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Disease on EC 3.1.3.3 - phosphoserine phosphatase

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DISEASE
TITLE OF PUBLICATION
LINK TO PUBMED
Acidosis
Cytochalasin D reduces Ca2+ currents via cofilin-activated depolymerization of F-actin in guinea-pig cardiomyocytes.
Acne Vulgaris
Evaluation of PSP technique including dot peeling, subcision and intradermal injection of PRP in the treatment of atrophic post-acne scars.
aconitate hydratase deficiency
Brain aconitase activity is not decreased in progressive supranuclear palsy.
Acquired Immunodeficiency Syndrome
Cognitive and magnetic resonance imaging aspects of corticobasal degeneration and progressive supranuclear palsy.
Long-term perspective on the prevalent-cohort biases in studies of human immunodeficiency virus progression.
Acute Kidney Injury
A validation of presepsin levels in kidney dysfunction patients: four case reports.
Rectal ulcer due to Kayexalate deposition - an unusual case.
Adenocarcinoma
A case of pulmonary sclerosing pneumocytoma diagnosed preoperatively using transbronchial cryobiopsy.
Human colon tumors: enzymic and histological characteristics.
Positive Resection Margins Detected by Standardized Study of a Pancreaticoduodenectomy Sample: Is There Any Real Impact on Long-term Survival?
Pulmonary sclerosing pneumocytoma with mediastinal lymph node metastasis: a case report.
Adenoma
Interendoscopist variability in proximal colon polyp detection is twice higher for serrated polyps than adenomas.
Pituitary tumors contain a side population with tumor stem cell-associated characteristics.
Relationships of parathyroid hormone, parathyroid secretory protein, parathyroid hormone messenger RNA, parathyroid secretory protein mRNA, and replication in human parathyroid adenoma and secondary hyperplasia tissues and cultures.
Adenoma, Pleomorphic
Pleomorphic adenoma: extracapsular dissection versus partial superficial parotidectomy with facial nerve dissection.
Agnosia
Cognitive disturbances in progressive supranuclear palsy.
Agraphia
Profile of children with poor school performance in Mumbai.
Akinetic Mutism
Vascular Parkinsonism: deconstructing a syndrome.
[The thalamic changes in progressive supranuclear palsy]
Alzheimer Disease
Action and object naming in frontotemporal dementia, progressive supranuclear palsy, and corticobasal degeneration.
Advances in progressive supranuclear palsy: new diagnostic criteria, biomarkers, and therapeutic approaches.
An association study of common variation at the MAPT locus with late-onset Alzheimer's disease.
An autopsy case of frontotemporal lobar degeneration with the appearance of fused in sarcoma inclusions (basophilic inclusion body disease) clinically presenting corticobasal syndrome.
Anti-tau phospho-specific Ser262 antibody recognizes a variety of abnormal hyper-phosphorylated tau deposits in tauopathies including Pick bodies and argyrophilic grains.
Antigenic characteristics of neurofibrillary tangles in progressive supranuclear palsy.
Applause sign: is it really specific for Parkinsonian disorders? Evidence from cortical dementias.
Argyrophilic grain disease is a sporadic 4-repeat tauopathy.
Argyrophilic grain disease: a late-onset dementia with distinctive features among tauopathies.
Assessment of 18F-PI-2620 as a Biomarker in Progressive Supranuclear Palsy.
Brain somatostatin concentrations do not decrease in progressive supranuclear palsy.
C9orf72 repeat expansions are restricted to the ALS-FTD spectrum.
Cerebrospinal fluid levels of neurogranin in Parkinsonian disorders.
Clinical and pathological study of two patients with progressive supranuclear palsy and Alzheimer's changes. Antigenic determinants that distinguish cortical and subcortical neurofibrillary tangles.
Constant neurofibrillary changes in the neocortex in progressive supranuclear palsy. Basic differences with Alzheimer's disease and aging.
CSF neurofilament light chain and phosphorylated tau 181 predict disease progression in PSP.
Cytokine expression and microglial activation in progressive supranuclear palsy.
Direct analysis of tau from PSP brain identifies new phosphorylation sites and a major fragment of N-terminally cleaved tau containing four microtubule-binding repeats.
Early Stage of Progressive Supranuclear Palsy: A Neuropathological Study of 324 Consecutive Autopsy Cases.
Essential tremor followed by progressive supranuclear palsy: postmortem reports of 11 patients.
Factors associated with development and distribution of granular/fuzzy astrocytes in neurodegenerative diseases.
Frontrunner in Translation: Progressive Supranuclear Palsy.
Haplotype-specific expression of exon 10 at the human MAPT locus.
Identification of a novel polymorphism in the promoter region of the tau gene highly associated to progressive supranuclear palsy in humans.
Increase in the relative expression of tau with four microtubule binding repeat regions in frontotemporal lobar degeneration and progressive supranuclear palsy brains.
Leucine Carboxyl Methyltransferase 1 Overexpression Protects Against Cognitive and Electrophysiological Impairments in Tg2576 APP Transgenic Mice.
Lewy bodies in progressive supranuclear palsy represent an independent disease process.
Lipoperoxidation is selectively involved in progressive supranuclear palsy.
Loss of pedunculopontine neurons in progressive supranuclear palsy.
Molecular genetics of chromosome 17 tauopathies.
Muscarinic receptors in the thalamus in progressive supranuclear palsy and other neurodegenerative disorders.
Mutations in bassoon in individuals with familial and sporadic progressive supranuclear palsy-like syndrome.
Neurofibrillary pathology in progressive supranuclear palsy (PSP).
Neurofibrillary tangles in progressive supranuclear palsy contain the same tau epitopes identified in Alzheimer's disease PHFtau.
Neuronal loss in the basal nucleus of Meynert in progressive supranuclear palsy.
Neuropathologic differentiation of progressive supranuclear palsy and corticobasal degeneration.
No evidence of CRHR1 gene involvement in progressive supranuclear palsy.
Oculomotor function in frontotemporal lobar degeneration, related disorders and Alzheimer's disease.
Overexpression of four-repeat tau mRNA isoforms in progressive supranuclear palsy but not in Alzheimer's disease.
Pathological, clinical and genetic heterogeneity in progressive supranuclear palsy.
Pattern of Tau forms in CSF is altered in progressive supranuclear palsy.
PET Tau Imaging and Motor Impairments Differ Between Corticobasal Syndrome and Progressive Supranuclear Palsy With and Without Alzheimer's Disease Biomarkers.
Phosphorylation and cleavage of tau in non-AD tauopathies.
Pittsburgh Compound B and AV-1451 positron emission tomography assessment of molecular pathologies of Alzheimer's disease in progressive supranuclear palsy.
Polymorphisms in the tau gene in sporadic frontotemporal dementia and other neurodegenerative disorders.
Preclinical and Clinical Development of ABBV-8E12, a Humanized Anti-Tau Antibody, for Treatment of Alzheimer's Disease and Other Tauopathies.
Preliminary NINDS neuropathologic criteria for Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy).
Progressive Supranuclear Palsy and Corticobasal Degeneration: Pathophysiology and Treatment Options.
Progressive supranuclear palsy often develops idiopathic normal pressure hydrocephalus-like magnetic resonance imaging features.
Progressive supranuclear palsy with fronto-temporal atrophy and various tau-positive abnormal structures.
Progressive supranuclear palsy with widespread cerebral lesions.
Progressive supranuclear palsy: neuropathologic and clinical heterogeneity.
Rates of cerebral atrophy differ in different degenerative pathologies.
Regional quantitative analysis of tau-positive neurons in progressive supranuclear palsy: comparison with Alzheimer's disease.
Relationship of the extended tau haplotype to tau biochemistry and neuropathology in progressive supranuclear palsy.
Role of serine/threonine protein phosphatase in Alzheimer's disease.
Stimulation over the cerebellum with a regular figure-of-eight coil induces reduced motor cortex inhibition in patients with progressive supranuclear palsy.
Substructure of 20 nm filaments of progressive supranuclear palsy.
Tau accumulation in astrocytes in progressive supranuclear palsy is a degenerative rather than a reactive process.
Tau and saitohin gene expression pattern in progressive supranuclear palsy.
Tau burden and the functional connectome in Alzheimer's disease and progressive supranuclear palsy.
Tau forms in CSF as a reliable biomarker for progressive supranuclear palsy.
Tau Imaging in the 4-Repeat-Tauopathies Progressive Supranuclear Palsy and Corticobasal Syndrome: A 11C-Pyridinyl-Butadienyl-Benzothiazole 3 PET Pilot Study.
Tau imaging with [(18) F]THK-5351 in progressive supranuclear palsy.
The basal ganglia cholinergic neurochemistry of progressive supranuclear palsy and other neurodegenerative diseases.
The midbrain-to-pons ratio distinguishes progressive supranuclear palsy from non-fluent primary progressive aphasias.
The neuropathology of progressive supranuclear palsy.
The pedunculopontine nucleus in Parkinson's disease, progressive supranuclear palsy and Alzheimer's disease.
The Role of Stress as a Risk Factor for Progressive Supranuclear Palsy.
The tau positron-emission tomography tracer AV-1451 binds with similar affinities to tau fibrils and monoamine oxidases.
The unfolded protein response is activated in disease-affected brain regions in progressive supranuclear palsy and Alzheimer's disease.
Traumatic Brain Injury and Firearm Use and Risk of Progressive Supranuclear Palsy Among Veterans.
[An autopsy case of postencephalitic parkinsonism: investigation on neurofibrillary tangles in comparison with those in progressive supranuclear palsy]
[Progressive nonfluent aphasia].
[Progressive supranuclear palsy-Richardson syndrome with visual attention disturbance (Holmes and Horrax) and ataxie optique (Garcin): a case report].
[Sleep in progressive supranuclear palsy]
[The genetics of corticobasal syndrome].
Amnesia
Progressive Supranuclear Palsy: What do we know About it?
Amyotrophic Lateral Sclerosis
Guadeloupean parkinsonism: a cluster of progressive supranuclear palsy-like tauopathy.
Human positron emission tomographic [18F]fluorodopa studies correlate with dopamine cell counts and levels.
Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases.
Progress in clinical neurosciences: Frontotemporal dementia-pick's disease.
The unfolded protein response is activated in disease-affected brain regions in progressive supranuclear palsy and Alzheimer's disease.
Under-recognized primary spontaneous pneumothorax in ALS: a multicenter retrospective study.
Aneurysm
Syndrome resembling PSP after surgical repair of ascending aorta dissection or aneurysm.
[A case of a syndrome resembling PSP after aortic arch replacement under deep hypothermic circulatory arrest].
Angina, Stable
The role of polysaccharide peptide of Ganoderma lucidum as a potent antioxidant against atherosclerosis in high risk and stable angina patients.
Anhedonia
Alexithymia and anhedonia in early Richardson's syndrome and progressive supranuclear palsy with predominant parkinsonism.
Major depressive disorder preceding the onset of progressive supranuclear palsy.
Negative symptoms and everyday functioning in schizophrenia: a cross-sectional study in a real world-setting.
Anosmia
Hyposmia in progressive supranuclear palsy.
Olfaction in Neuropathologically Defined Progressive Supranuclear Palsy.
Olfactory function in idiopathic Parkinson's disease (IPD): results from cross-sectional studies in IPD patients and long-term follow-up of de-novo IPD patients.
Anovulation
A single dose of mifepristone induces ovulation in pseudopregnant rats.
Anthracosis
Fluorescein-enhanced Autofluorescence Thoracoscopy in Patients with Primary Spontaneous Pneumothorax and Normal Subjects.
Aphasia
A case of atypical progressive supranuclear palsy.
Aphasia in Progressive Supranuclear Palsy: As Severe as Progressive Non-Fluent Aphasia.
Beyond the midbrain atrophy: wide spectrum of structural MRI finding in cases of pathologically proven progressive supranuclear palsy.
Clinical features differentiating patients with postmortem confirmed progressive supranuclear palsy and corticobasal degeneration.
Clinical use of SAND battery to evaluate language in patients with Progressive Supranuclear Palsy.
Clinicopathologic analysis of frontotemporal and corticobasal degenerations and PSP.
Cognitive disturbances in progressive supranuclear palsy.
Extrapyramidal syndromes in frontotemporal degeneration.
Family history of frontotemporal lobar degeneration in Asia - an international multi-center research.
First symptom guides diagnosis and prognosis in neurodegenerative diseases-a retrospective study of autopsy proven cases.
Frontal dynamic aphasia in progressive supranuclear palsy: Distinguishing between generation and fluent sequencing of novel thoughts.
Negative symptoms and everyday functioning in schizophrenia: a cross-sectional study in a real world-setting.
Oculomotor function in frontotemporal lobar degeneration, related disorders and Alzheimer's disease.
Pattern of behavioral disturbances in corticobasal degeneration syndrome and progressive supranuclear palsy.
Progressive Supranuclear Palsy: What do we know About it?
The midbrain-to-pons ratio distinguishes progressive supranuclear palsy from non-fluent primary progressive aphasias.
The overlapping syndromes of the pick complex.
Aphasia, Broca
Apraxia of speech and nonfluent aphasia: a new clinical marker for corticobasal degeneration and progressive supranuclear palsy.
Aphasia, Primary Progressive
Action and object naming in frontotemporal dementia, progressive supranuclear palsy, and corticobasal degeneration.
Language impairment in progressive supranuclear palsy and corticobasal syndrome.
Progressive supranuclear palsy presenting with primary progressive aphasia--clinicopathological report of an autopsy case.
Relationship between frontotemporal dementia and corticobasal degeneration/progressive supranuclear palsy.
[A 62-year-old Woman Presenting with Progressive Nonfluent Aphasia, Apraxia of Eyelid Opening, Supranuclear Gaze Palsy, and Asymmetric Rigidity].
[Corticobasal degeneration and atypical progressive supranuclear palsy: their symptomatology, laboratory examination and differential diagnosis]
Apnea
Effects of neural drives on breathing in the awake state in humans.
Apraxia, Ideomotor
Apraxia in Parkinson's disease, progressive supranuclear palsy, multiple system atrophy and neuroleptic-induced parkinsonism.
Clinical features differentiating patients with postmortem confirmed progressive supranuclear palsy and corticobasal degeneration.
Cognitive and magnetic resonance imaging aspects of corticobasal degeneration and progressive supranuclear palsy.
Cognitive dysfunction and impaired organization of complex motility in degenerative parkinsonian syndromes.
Cognitive dysfunction associated with falls in progressive supranuclear palsy.
Distal-proximal differences in limb apraxia in corticobasal degeneration but not progressive supranuclear palsy.
Limb apraxia and cognitive impairment in progressive supranuclear palsy.
Limb apraxia in corticobasal degeneration and progressive supranuclear palsy.
Motor, cognitive and behavioral differences in MDS PSP phenotypes.
Somatosensory evoked potentials in progressive supranuclear palsy.
Apraxias
A case of atypical progressive supranuclear palsy.
Apraxia in movement disorders.
Apraxia in Parkinson's disease, progressive supranuclear palsy, multiple system atrophy and neuroleptic-induced parkinsonism.
Apraxia of speech and nonfluent aphasia: a new clinical marker for corticobasal degeneration and progressive supranuclear palsy.
Autopsy-proven progressive supranuclear palsy presenting as behavioral variant frontotemporal dementia.
Cognitive disturbances in progressive supranuclear palsy.
Comparison of clinical features in pathologically confirmed PSP and MSA patients followed at a tertiary center.
Extrapyramidal syndromes in frontotemporal degeneration.
How to spot ocular abnormalities in progressive supranuclear palsy? A practical review.
Increased tau burden in the cortices of progressive supranuclear palsy presenting with corticobasal syndrome.
Language impairment in progressive supranuclear palsy and corticobasal syndrome.
Limb apraxia and cognitive impairment in progressive supranuclear palsy.
Limb apraxia in corticobasal degeneration and progressive supranuclear palsy.
Long-term locomotor training for gait and balance in a patient with mixed progressive supranuclear palsy and corticobasal degeneration.
Motor Speech Disorders and Communication Limitations in Progressive Supranuclear Palsy.
Neuropathology of variants of progressive supranuclear palsy.
Progressive supranuclear palsy and corticobasal degeneration: lumping versus splitting.
Quantitative evaluation of oculomotor disturbances in progressive supranuclear palsy.
The evolution of parkinsonism in primary progressive apraxia of speech: A 6-year longitudinal study.
[A 68-year-old man with speech disturbance as the initial symptom followed by bradykinesia and dementia. Clinical conference]
[A case of progressive supranuclear palsy presenting mouth opening difficulty with tonic contraction of the orbicularis oris muscle]
[Progressive supranuclear palsy with macular degeneration--report of three cases]
[Progressive supranuclear palsy: what's new?].
Arthritis
Patient Support Program Increased Medication Adherence with Lower Total Health Care Costs Despite Increased Drug Spending.
Arthritis, Psoriatic
Patient Support Program Increased Medication Adherence with Lower Total Health Care Costs Despite Increased Drug Spending.
Astrocytoma
Analysis of pseudoprogression after proton or photon therapy of 99 patients with low grade and anaplastic glioma.
Ataxia
Comparison of clinical features in pathologically confirmed PSP and MSA patients followed at a tertiary center.
Effect of verapamil on organophosphorus-induced delayed neuropathy in hens.
Effects of organophosphate phenyl saligenin phosphate and polyether carboxylic ionophore lasalocid on motor nerve conduction velocity, neuropathy target esterase enzyme activity, and clinical ataxia in chickens.
Modification of phenyl saligenin phosphate-induced delayed effects by calcium channel blockers: in vivo and in vitro electrophysiological assessment.
Progressive Supranuclear Palsy with Predominant Cerebellar Ataxia.
Types of adrenocorticoids and their effect on organophosphorus-induced delayed neuropathy in chickens.
Atherosclerosis
Decreasing angiogenesis vasa vasorum through Lp-PLA2 and H2O2 inhibition by PSP from Ganoderma lucidum in atherosclerosis: in vivo diabetes mellitus type 2.
The reduction of aorta histopathological images through inhibition of reactive oxygen species formation in hypercholesterolemia rattus norvegicus treated with polysaccharide peptide of Ganoderma lucidum.
The role of polysaccharide peptide of Ganoderma lucidum as a potent antioxidant against atherosclerosis in high risk and stable angina patients.
Atrial Fibrillation
Alterations in the interactome of serine/threonine protein phosphatase type-1 in atrial fibrillation patients.
Post-stroke pneumonia at the stroke unit - a registry based analysis of contributing and protective factors.
Prolonged Sinus Pauses upon Termination of Paroxysmal Atrial Fibrillation: Abnormal Right Atrial Electrophysiologic and Electroanatomic Findings.
Risk factors for and impact of poststroke pneumonia in patients with acute ischemic stroke.
Risk stratification model for post-stroke pneumonia in patients with acute ischemic stroke.
Autoimmune Diseases
Autoantibodies, detection methods and panels for diagnosis of Sjögren's syndrome.
Polysaccharopeptide mimics ciclosporin-mediated Th1/Th2 cytokine balance for suppression of activated human T cell proliferation by MAPKp38 and STAT5 pathways.
Regulatory properties of polysaccharopeptide derived from Coriolus versicolor and its combined effect with ciclosporin on the homeostasis of human lymphocytes.
Azotemia
Relationship of selected clinical renal function tests to glomerular filtration rate and renal blood flow in cats.
Bacterial Infections
Clinical application of presepsin as diagnostic biomarker of infection: overview and updates.
Plasmatocyte-spreading peptide (PSP) plays a central role in insect cellular immune defenses against bacterial infection.
Basal Ganglia Diseases
CT findings in progressive supranuclear palsy.
Pattern of Tau forms in CSF is altered in progressive supranuclear palsy.
Progressive supranuclear palsy: clinico-pathological and biochemical studies.
Biliary Fistula
[Benign obstruction of the common bile duct: what is the current role of transduodenal sphincteroplasty?]
Birt-Hogg-Dube Syndrome
Mutation analysis of the FLCN gene in Chinese patients with sporadic and familial isolated primary spontaneous pneumothorax.
Blepharospasm
Dystonia in Parkinson's disease, multiple system atrophy, and progressive supranuclear palsy.
Eyelid motor abnormalities in progressive supranuclear palsy.
How to spot ocular abnormalities in progressive supranuclear palsy? A practical review.
Blister
A 4-bp deletion in the Birt-Hogg-Dubé gene (FLCN) causes dominantly inherited spontaneous pneumothorax.
A deep azygoesophageal recess may increase the risk of secondary spontaneous pneumothorax.
Alveolar epithelial permeability in patients with primary spontaneous pneumothorax as determined by Tc-99m DTPA aerosol scintigraphy.
Association between postoperative bulla neogenesis at the staple line and resected lung weight for primary spontaneous pneumothorax: a retrospective study using the inverse-probability of treatment weighted method in patients grouped according to age.
Association of MMP-2 and MMP-9 expression with recurrences in primary spontaneous pneumothorax.
Bilateral primary spontaneous pneumothorax with multiple bleb performed by VATS and wedge resection: A rare case in Indonesian adult and review article.
Can CT scanning be used to select patients with unilateral primary spontaneous pneumothorax for bilateral surgery?
Comparison of additional minocycline versus iodopovidone pleurodesis during video-assisted thoracoscopic bleb resection for primary spontaneous pneumothorax: a propensity score-matched analysis.
Contralateral bulla neogenesis associated with postoperative recurrences of primary spontaneous pneumothorax in young patients.
Correlation of matrix metalloproteinase-2 and -9 expression with recurrences in primary spontaneous pneumothorax patients.
Do Blebs or Bullae on High-Resolution Computed Tomography Predict Ipsilateral Recurrence in Young Patients at the First Episode of Primary Spontaneous Pneumothorax?
Efficacy of blebs detection for preventive surgery in children's idiopathic spontaneous pneumothorax.
ERS task force statement: diagnosis and treatment of primary spontaneous pneumothorax.
Evidence-based management of paediatric primary spontaneous pneumothorax.
Expression of TGF-beta receptor 1 and Smads in the tissues of primary spontaneous pneumothorax.
First Episode of Spontaneous Pneumothorax: CT-based Scoring to Select Patients for Early Surgery.
High-Resolution CT Following Primary Spontaneous Pneumothorax in Adolescents: Useful Tool or Wasted Radiation?
Influence of lung resection volume on risk of primary spontaneous pneumothorax recurrence.
Is it a myth to perform blind apical wedge resection in primary spontaneous pneumothorax surgery to improve recurrence rates?
Male adolescents with contralateral blebs undergoing surgery for primary spontaneous pneumothorax may benefit from simultaneous contralateral blebectomies.
Metachronous recurrent pediatric primary spontaneous pneumothorax: A case presentation and literature review.
Natural Course of Spontaneous Pneumothorax without Bullae or Blebs under High-Resolution Computed Tomography.
Neo-generation of neogenetic bullae after surgery for spontaneous pneumothorax in young adults: a prospective study.
New insights and improved strategies for the management of primary spontaneous pneumothorax.
One hundred consecutive cases of video-assisted thoracoscopic surgery for primary spontaneous pneumothorax.
Outcomes of Contralateral Bullae in Primary Spontaneous Pneumothorax.
Physical fitness after apical resection for the treatment of primary spontaneous pneumothorax.
Primary spontaneous pneumothorax in children: factors predicting recurrence and contralateral occurrence.
Primary spontaneous pneumothorax in children: the role of CT in guiding management.
Relationship between postoperative bulla neogenesis at the staple line and the resected lung volume in primary spontaneous pneumothorax.
Results of thoracoscopic pleural abrasion for primary spontaneous pneumothorax.
Role of Blebs and Bullae Detected by High-Resolution Computed Tomography and Recurrent Spontaneous Pneumothorax.
Severity of Pectus Excavatum is a Risk Factor for Primary Spontaneous Pneumothorax.
Should We Consider the Resected Lung Volume in Primary Spontaneous Pneumothorax?
Simultaneous Bilateral Video-Assisted Thoracoscopic Surgery for the Treatment of Primary Spontaneous Pneumothorax.
Surgical Intervention for Primary Spontaneous Pneumothorax in Pediatric Population: When and Why?
The Presence of a Reticulated Trabecula-Like Structure Increases the Risk for the Recurrence of Primary Spontaneous Pneumothorax after Thoracoscopic Bullectomy.
Unilateral single-port thoracoscopic surgery for bilateral pneumothorax or pulmonary bullae.
Uniportal approach as an alternative to the three-portal approach to video-assisted thoracic surgery for primary spontaneous pneumothorax.
Value of computer tomography in the detection of bullae and blebs in patients with primary spontaneous pneumothorax.
Vascular-penetration defect detected in parietal pleura of primary spontaneous pneumothorax.
Video-assisted extrathoracic bleb excision: An ultra-minithoracotomy for primary spontaneous pneumothorax.
Video-assisted thoracoscopic surgery (VATS) for bilateral primary spontaneous pneumothorax.
Video-assisted thoracoscopic surgery for primary spontaneous pneumothorax: clinicopathological correlation.
Video-assisted thoracoscopic suture closure of blebs to treat primary spontaneous pneumothorax.
Videothoracoscopic treatment of primary spontaneous pneumothorax: a 6-year experience.
What Factors Predict Recurrence after an Initial Episode of Primary Spontaneous Pneumothorax in Children?
Bone Diseases, Metabolic
Abnormal bone mineral density and bone turnover marker expression profiles in patients with primary spontaneous pneumothorax.
Bone Resorption
Abnormal bone mineral density and bone turnover marker expression profiles in patients with primary spontaneous pneumothorax.
Role of Porphyromonas gingivalis phosphoserine phosphatase enzyme SerB in inflammation, immune response, and induction of alveolar bone resorption in rats.
Botulism
[Clinical analysis of paralytic shellfish poisoning following ingestion of oysters]
Bradycardia
Perinatal and infant outcomes of prenatal diagnosis of heterotaxy syndrome (asplenia and polysplenia).
Brain Diseases
Parkinsonian Syndrome with Frontal Lobe Involvement and Anti-Glycine Receptor Antibodies.
Positron emission tomography study in progressive supranuclear palsy. Brain hypometabolic pattern and clinicometabolic correlations.
Typical cerebral metabolic patterns in neurodegenerative brain diseases.
Vascular Parkinsonism: deconstructing a syndrome.
Brain Injuries
Cerebrospinal Fluid Presepsin As a Marker of Nosocomial Infections of the Central Nervous System: A Prospective Observational Study.
Brain Injuries, Traumatic
Traumatic Brain Injury and Firearm Use and Risk of Progressive Supranuclear Palsy Among Veterans.
Brain Ischemia
Parkinsonian syndromes associated with hydrocephalus: case reports, a review of the literature, and pathophysiological hypotheses.
Brain Neoplasms
Diagnostic value of radiolabeled amino acid PET for detection of pseudoprogression of brain tumor after treatment: a meta-analysis.
Breast Neoplasms
A murine preclinical syngeneic transplantation model for breast cancer precision medicine.
Anti- RI antibody associated progressive supranuclear palsy like presentation in a patient with breast carcinoma.
Cell cycle-independent regulation of p21Waf1/Cip1 and retinoblastoma protein during okadaic acid-induced apoptosis is coupled with induction of Bax protein in human breast carcinoma cells.
Combination of zoledronic acid and serine/threonine phosphatase inhibitors induces synergistic cytotoxicity and apoptosis in human breast cancer cells via inhibition of PI3K/Akt pathway.
Growth stimulatory effect of pancreatic spasmolytic polypeptide on cultured colon and breast tumor cells.
Long-term incidence of breast cancer by trial arm in one county of the Swedish Two-County Trial of mammographic screening.
Oncogenic properties of PPM1D located within a breast cancer amplification epicenter at 17q23.
Polysaccharide peptide mediates apoptosis by up-regulating p21 gene and down-regulating cyclin D1 gene.
Polysaccharopeptide enhances the anticancer activity of doxorubicin and etoposide on human breast cancer cells ZR-75-30.
PPM1B depletion in U2OS cells supresses cell growth through RB1-E2F1 pathway and stimulates bleomycin-induced cell death.
The relative contributions of screen-detected in situ and invasive breast carcinomas in reducing mortality from the disease.
The Swedish Two-County Trial of mammographic screening: cluster randomisation and end point evaluation.
Bronchiectasis
Multifocal neuroendocrine cell hyperplasia accompanied by tumorlet formation and pulmonary sclerosing pneumocytoma: A case report.
Bronchiolitis
New insights and improved strategies for the management of primary spontaneous pneumothorax.
Bronchitis, Chronic
Coriolus versicolor polysaccharopeptide as an immunotherapeutic in China.
Bulbar Palsy, Progressive
Progressive supranuclear palsy.
[Progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): report of a case and review of the literature]
Carcinogenesis
Phosphatase Wip1 as a new therapeutic target for intestinal ischemia-reperfusion injury.
[Minisatellite instability induced by okadaic acid]
Carcinoid Tumor
68Ga-DOTATATE-avid pulmonary sclerosing pneumocytoma in a man of North African descent: Case report, imaging findings and pathology.
A case of pulmonary sclerosing pneumocytoma diagnosed preoperatively using transbronchial cryobiopsy.
Carcinoma
Differences in association of the serine/threonine protein phosphatase PP-2A with microtubules of metastatic and nonmetastatic tumor cells.
Dihydroxyphenylethanol induces apoptosis by activating serine/threonine protein phosphatase PP2A and promotes the endoplasmic reticulum stress response in human colon carcinoma cells.
Early progressive supranuclear palsy: pathology and clinical presentation.
Enhancing the utility of Proteomics Signature Profiling (PSP) with Pathway Derived Subnets (PDSs), performance analysis and specialised ontologies.
Enzyme pathology of human mesotheliomas.
FLCN-regulated miRNAs suppressed reparative response in cells and pulmonary lesions of Birt-Hogg-Dubé syndrome.
Inducible expression of catalytically active type 1 serine/threonine protein phosphatase in a human carcinoma cell line.
Paraneoplastic syndrome mimicking progressive supranuclear palsy.
Radical resection of gastric carcinoma with pancreas and spleen preservation and functional cleaning of lymph nodes.
Serine/threonine protein phosphatase type 1gamma1 is required for the completion of cytokinesis in human A549 lung carcinoma cells.
[A fluorescent dye method based on changes in membrane potential for detecting PSP toxins in shellfish]
[Analysis of Clinical Characteristics of 35 Cases ?of Pulmonary Sclerosing Pneumocytoma].
[Resection of gastric carcinoma with preserving of the spleen and pancreas and functional clearance lymph nodes of the spleen hillus and splenic artery]
Carcinoma, Hepatocellular
cMyc-mediated activation of serine biosynthesis pathway is critical for cancer progression under nutrient deprivation conditions.
Down regulation of a novel protein, PSP, in rat hepatoma cdRLh 84-beared tumor.
Recombinant expression of perchloric acid-soluble protein reduces cell proliferation.
Carcinoma, Lewis Lung
Differences in association of the serine/threonine protein phosphatase PP-2A with microtubules of metastatic and nonmetastatic tumor cells.
Carcinoma, Non-Small-Cell Lung
Enhancing the utility of Proteomics Signature Profiling (PSP) with Pathway Derived Subnets (PDSs), performance analysis and specialised ontologies.
Upregulation of phosphoserine phosphatase contributes to tumor progression and predicts poor prognosis in non-small cell lung cancer patients.
Carcinoma, Renal Cell
FLCN-regulated miRNAs suppressed reparative response in cells and pulmonary lesions of Birt-Hogg-Dubé syndrome.
Carcinoma, Small Cell
Paraneoplastic syndrome mimicking progressive supranuclear palsy.
Carcinoma, Squamous Cell
[Analysis of Clinical Characteristics of 35 Cases ?of Pulmonary Sclerosing Pneumocytoma].
Carcinoma, Transitional Cell
[A fluorescent dye method based on changes in membrane potential for detecting PSP toxins in shellfish]
Cardiomegaly
Four and a half LIM domain protein signaling and cardiomyopathy.
Functional and phenotypic relevance of differentially expressed proteins in calcineurin mutants of Caenorhabditis elegans.
Multiple domains of MCIP1 contribute to inhibition of calcineurin activity.
Protein kinase-mediated regulation of calcineurin through the phosphorylation of modulatory calcineurin-interacting protein 1.
Structures of calcineurin and its complexes with immunophilins-immunosuppressants.
The essential role of MEKK3 signaling in angiotensin II-induced calcineurin/nuclear factor of activated T-cells activation.
The role of modulatory calcineurin-interacting proteins in calcineurin signaling.
Cardiovascular Diseases
A Random Forest Model for Predicting Social Functional Improvement in Chinese Patients with Schizophrenia After 3 Months of Atypical Antipsychotic Monopharmacy: A Cohort Study.
ECHOCARDIOGRAPHIC CHARACTERISTICS OF DIFFERENT WHO/ISH CARDIOVASCULAR DISEASE RISK GROUPS.
Cardiovascular Infections
Clinical application of presepsin as diagnostic biomarker of infection: overview and updates.
Cataract
[Experimental study of changes in the pressure of the posterior segment of the eye under general anesthesia. Consequences for surgery of the anterior segment]
Cellulitis
Which outcomes are reported in cellulitis trials? Results of a review of outcomes included in cellulitis trials and a patient priority setting survey.
Cerebellar Ataxia
Beyond the midbrain atrophy: wide spectrum of structural MRI finding in cases of pathologically proven progressive supranuclear palsy.
Cerebellar dentate nucleus in progressive supranuclear palsy.
Cerebellar involvement in progressive supranuclear palsy: A clinicopathological study.
Deterioration of horizontal saccades in progressive supranuclear palsy.
Differences in cerebellar perfusion between Parkinson's disease and multiple system atrophy.
Effects of cerebellar neuromodulation in movement disorders: A systematic review.
FTLD-TDP and progressive supranuclear palsy in comorbidity-a report of two cases with different clinical presentations.
Progressive Supranuclear Gaze Palsy with Predominant Cerebellar Ataxia: A Case Series with Videos.
Progressive Supranuclear Palsy with Predominant Cerebellar Ataxia.
The linear vestibulo-ocular reflex, locomotion and falls in neurological disorders.
Unusual phenotype of pathologically confirmed progressive supranuclear palsy with autonomic dysfunction and cerebellar ataxia: Case report.
When DLB, PD, and PSP masquerade as MSA: an autopsy study of 134 patients.
Cerebellar Diseases
Automated Brainstem Segmentation Detects Differential Involvement in Atypical Parkinsonian Syndromes.
Deciphering the saccade velocity profile of progressive supranuclear palsy: A sign of latent cerebellar/brainstem dysfunction?
Cerebral Amyloid Angiopathy
Progressive supranuclear palsy and a multi-infarct state.
Cerebral Cortical Thinning
18F-AV1451 PET imaging and multimodal MRI changes in progressive supranuclear palsy.
Integrated 18F-T807 Tau PET, Structural MRI, and Plasma Tau in Tauopathy Neurodegenerative Disorders.
Cerebral Infarction
Multi-infarct progressive supranuclear palsy--case report.
Protective effect of polysaccharide peptide on cerebral ischemia?reperfusion injury in rats.
Risk factors for and impact of poststroke pneumonia in patients with acute ischemic stroke.
Cerebrovascular Disorders
Clinical Features Observed in General Practice Associated With the Subsequent Diagnosis of Progressive Supranuclear Palsy.
Copathology in Progressive Supranuclear Palsy: Does It Matter?
Lack of association between progressive supranuclear palsy and arterial hypertension: a clinicopathological study.
No evidence of CRHR1 gene involvement in progressive supranuclear palsy.
Vascular progressive supranuclear palsy.
Cholangiocarcinoma
Comparison of intraluminal radiofrequency ablation and stents vs. stents alone in the management of malignant biliary obstruction.
Cholera
Regulation of the transmodulated epidermal growth factor receptor by cholera toxin and the protein phosphatase inhibitor okadaic acid.
Chronic Traumatic Encephalopathy
Advances in progressive supranuclear palsy: new diagnostic criteria, biomarkers, and therapeutic approaches.
Frontrunner in Translation: Progressive Supranuclear Palsy.
Colitis, Ulcerative
Patient Support Program Increased Medication Adherence with Lower Total Health Care Costs Despite Increased Drug Spending.
Colonic Neoplasms
Alterations of the PPP2R1B gene located at 11q23 in human colorectal cancers.
Birt-Hogg-Dube Syndrome with a Novel Mutation in the FLCN Gene.
Colorectal Neoplasms
A 4-bp deletion in the Birt-Hogg-Dubé gene (FLCN) causes dominantly inherited spontaneous pneumothorax.
Gene mutations in stool from gastric and colorectal neoplasia patients by next-generation sequencing.
Inhibition of phosphoserine phosphatase enhances the anticancer efficacy of 5-fluorouracil in colorectal cancer.
Phosphoserine Phosphatase Is a Novel Prognostic Biomarker on Chromosome 7 in Colorectal Cancer.
Communicable Diseases
Presepsin in risk stratification of SARS-CoV-2 patients.
Complex Regional Pain Syndromes
Poststroke Pain.
Confusion
Health-related quality of life in patients with progressive supranuclear palsy.
Limited usefulness of electroconvulsive therapy in progressive supranuclear palsy.
PATH47 Slow saccades in bulbar-onset motor neuron disease.
qPCR assays for Alexandrium fundyense and A. ostenfeldii (Dinophyceae) identified from Alaskan waters and a review of species-specific Alexandrium molecular assays.
Congenital Abnormalities
A meta-analysis of the pros and cons of partial superficial parotidectomy versus superficial parotidectomy for the treatment of benign parotid neoplasms.
Anesthetic management of a patient with progressive supranuclear palsy.
Joint and skeletal deformities in Parkinson's disease, multiple system atrophy, and progressive supranuclear palsy.
Risk of Primary Spontaneous Pneumothorax According to Chest Configuration.
Contracture
Erratum to: Novel Report of Phosphoserine Phosphatase Deficiency in an Adult with Myeloneuropathy and Limb Contractures.
Novel Report of Phosphoserine Phosphatase Deficiency in an Adult with Myeloneuropathy and Limb Contractures.
Corticobasal Degeneration
A combination of CSF tau ratio and midsaggital midbraintopons atrophy for the early diagnosis of progressive supranuclear palsy.
A novel diagnostic marker for progressive supranuclear palsy targeting atrophy of the subthalamic nucleus.
Accuracy of the National Institute for Neurological Disorders and Stroke/Society for Progressive Supranuclear Palsy and Neuroprotection and Natural History in Parkinson Plus Syndromes Criteria for the Diagnosis of Progressive Supranuclear Palsy.
An autopsy case of frontotemporal lobar degeneration with the appearance of fused in sarcoma inclusions (basophilic inclusion body disease) clinically presenting corticobasal syndrome.
Anti-tau phospho-specific Ser262 antibody recognizes a variety of abnormal hyper-phosphorylated tau deposits in tauopathies including Pick bodies and argyrophilic grains.
APOE ?2 is associated with increased tau pathology in primary tauopathy.
Applause sign in Parkinsonian disorders and Huntington's disease.
Apraxia of speech and nonfluent aphasia: a new clinical marker for corticobasal degeneration and progressive supranuclear palsy.
Argyrophilic grain disease: a late-onset dementia with distinctive features among tauopathies.
Association of PSP phenotypes with survival: A brain-bank study.
Automated Brainstem Segmentation Detects Differential Involvement in Atypical Parkinsonian Syndromes.
Beyond the midbrain atrophy: wide spectrum of structural MRI finding in cases of pathologically proven progressive supranuclear palsy.
Blood-based NfL: A biomarker for differential diagnosis of parkinsonian disorder.
Brain MR Contribution to the Differential Diagnosis of Parkinsonian Syndromes: An Update.
Cerebral blood flow in corticobasal degeneration and progressive supranuclear palsy.
Cerebral peduncle angle: Unreliable in differentiating progressive supranuclear palsy from other neurodegenerative diseases.
Cerebrospinal fluid levels of neurogranin in Parkinsonian disorders.
Characteristics of progressive supranuclear palsy presenting with corticobasal syndrome: a cortical variant.
Clinical and pathologic evidence of corticobasal degeneration and progressive supranuclear palsy in familial tauopathy.
Clinical features of dystonia in atypical parkinsonism.
Co-morbidity of progressive supranuclear palsy and amyotrophic lateral sclerosis: a clinical-pathological case report.
Consecutive analyses of cerebrospinal fluid axonal and glial markers in Parkinson's disease and atypical parkinsonian disorders.
Conventional magnetic resonance imaging in confirmed progressive supranuclear palsy and multiple system atrophy.
Cortical ballooned neurons in progressive supranuclear palsy.
CSF sAPP? and sAPP? levels in Alzheimer's Disease and Multiple Other Neurodegenerative Diseases: A Network Meta-Analysis.
Development and assessment of sensitive immuno-PCR assays for the quantification of cerebrospinal fluid three- and four-repeat tau isoforms in tauopathies.
Direct analysis of tau from PSP brain identifies new phosphorylation sites and a major fragment of N-terminally cleaved tau containing four microtubule-binding repeats.
Distinct Lysosomal Network Protein Profiles in Parkinsonian Syndrome Cerebrospinal Fluid.
Early Stage of Progressive Supranuclear Palsy: A Neuropathological Study of 324 Consecutive Autopsy Cases.
Environmental Risk Factors for Progressive Supranuclear Palsy.
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases.
Family history of frontotemporal lobar degeneration in Asia - an international multi-center research.
Frontrunner in Translation: Progressive Supranuclear Palsy.
High-Contrast In Vivo Imaging of Tau Pathologies in Alzheimer's and Non-Alzheimer's Disease Tauopathies.
Is brain perfusion a differentiating feature in the comparison of Progressive Supranuclear Palsy Syndrome (PSPS) and Corticobasal Syndrome (CBS)?
Late-onset Niemann-Pick disease type C overlapping with frontotemporal dementia syndromes: a case report.
Metabolic network expression in parkinsonism: Clinical and dopaminergic correlations.
Microtubule-associated protein tau genetic variations are uncommon cause of frontotemporal dementia in south India.
Molecular pathology and synaptic loss in primary tauopathies: an 18F-AV-1451 and 11C-UCB-J PET study.
Motor, cognitive and behavioral differences in MDS PSP phenotypes.
MRI for the differential diagnosis of neurodegenerative parkinsonism in clinical practice.
MRI gray and white matter measures in progressive supranuclear palsy and corticobasal syndrome.
Neuroimaging of PD, PSP, CBD and MSA-PET and SPECT studies.
Neuronal correlates of clinical asymmetry in progressive supranuclear palsy.
Neuropathological comorbidity associated with argyrophilic grain disease.
Neuropathology of variants of progressive supranuclear palsy.
Pathologic correlates of supranuclear gaze palsy with parkinsonism.
Pattern of Tau forms in CSF is altered in progressive supranuclear palsy.
Preferential neurodegeneration in the cervical spinal cord of progressive supranuclear palsy.
Primary Tau Pathology, Not Copathology, Correlates With Clinical Symptoms in PSP and CBD.
Profound degeneration of wake-promoting neurons in Alzheimer's disease.
Progressive supranuclear palsy presenting with hyperkinetic movement disorder and hemiplegic dystonia: a case report.
Progressive supranuclear palsy with fronto-temporal atrophy and various tau-positive abnormal structures.
Progressive supranuclear palsy.
Pyramidal system involvement in progressive supranuclear palsy - a clinicopathological correlation.
Relationship between frontotemporal dementia and corticobasal degeneration/progressive supranuclear palsy.
Side effects induced by the acute levodopa challenge in Parkinson's Disease and atypical parkinsonisms.
Stimulation over the cerebellum with a regular figure-of-eight coil induces reduced motor cortex inhibition in patients with progressive supranuclear palsy.
Structural basis of dementia in neurodegenerative disorders.
Study of LRRK2 variation in tauopathy: Progressive supranuclear palsy and corticobasal degeneration.
Tau forms in CSF as a reliable biomarker for progressive supranuclear palsy.
The evolution and pathology of frontotemporal dementia.
The midbrain-to-pons ratio distinguishes progressive supranuclear palsy from non-fluent primary progressive aphasias.
The Relationship Between Development of Neuronal and Astrocytic Tau Pathologies in Subcortical Nuclei and Progression of Argyrophilic Grain Disease.
The Value of GRE, ADC and Routine MRI in Distinguishing Parkinsonian Disorders.
Transcranial sonography in atypical parkinsonism: How reliable is it in real clinical practice? A multicentre comprehensive study.
Ultrastructural characteristics of tau filaments in tauopathies: immuno-electron microscopic demonstration of tau filaments in tauopathies.
Ultrastructural characterization of the tau-immunoreactive tubules in the oligodendroglial perikarya and their inner loop processes in progressive supranuclear palsy.
Unexpected abundance of pathological tau in progressive supranuclear palsy white matter.
Unilateral perseveration.
Untangling the tau gene association with neurodegenerative disorders.
Voxel-based comparison of regional cerebral glucose metabolism between PSP and corticobasal degeneration.
What can artificial neural networks teach us about neurodegenerative disorders with extrapyramidal features?
Which ante mortem clinical features predict progressive supranuclear palsy pathology?
Which clinical features differentiate progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) from related disorders? A clinicopathological study.
[A 57-year-old woman with progressive disturbance of gait and mental deterioration]
[A 62-year-old Woman Presenting with Progressive Nonfluent Aphasia, Apraxia of Eyelid Opening, Supranuclear Gaze Palsy, and Asymmetric Rigidity].
[A 68-year-old man with speech disturbance as the initial symptom followed by bradykinesia and dementia. Clinical conference]
[Progressive supranuclear palsy-Richardson syndrome with visual attention disturbance (Holmes and Horrax) and ataxie optique (Garcin): a case report].
[Progressive supranuclear palsy: what's new?].
[Progressive supranuclear palsy]
[The application of Gallyas-Braak stainings in pathologic diagnosis of neurodegenerative diseases]
Cough
Analysis of the clinical differentiation of pulmonary sclerosing pneumocytoma and lung cancer.
Comparison of tracheal intubation with controlled ventilation and laryngeal mask airway with spontaneous ventilation for thoracoscopic bullectomy.
Cough reflex attenuation and swallowing dysfunction in sub-acute post-stroke patients: prevalence, risk factors, and clinical outcome.
Immediate Effects of Sensorimotor Training in Airway Protection (smTAP) on Cough Outcomes in Progressive Supranuclear Palsy: A Feasibility Study.
Sensorimotor Cough Dysfunction Is Prevalent and Pervasive in Progressive Supranuclear Palsy.
The Role of Vocal Fold Bowing on Cough and Swallowing Dysfunction in Progressive Supranuclear Palsy.
COVID-19
How Have Public Safety Personnel Seeking Digital Mental Healthcare Been Affected by the COVID-19 Pandemic? An Exploratory Mixed Methods Study.
Periphery-aware COVID-19 diagnosis with contrastive representation enhancement.
Presepsin in risk stratification of SARS-CoV-2 patients.
Craniocerebral Trauma
Follow-up study of risk factors in progressive supranuclear palsy.
Creutzfeldt-Jakob Syndrome
Creutzfeldt-Jakob disease presenting as progressive supranuclear palsy.
[The genetics of corticobasal syndrome].
Crohn Disease
Patient Support Program Increased Medication Adherence with Lower Total Health Care Costs Despite Increased Drug Spending.
Cross Infection
[The use of data on the composition and drug resistance of the causative agents of suppuration in a retrospective analysis of the epidemiological situation in a hospital]
Cysts
Determination of paralytic shellfish toxins in Portuguese shellfish by automated pre-column oxidation.
Dynamics of Alexandrium fundyense blooms and shellfish toxicity in the Nauset Marsh System of Cape Cod (Massachusetts, USA).
Evidence-based management of paediatric primary spontaneous pneumothorax.
Promoter methylation is not associated with FLCN irregulation in lung cyst lesions of primary spontaneous pneumothorax.
Pulmonary sclerosing pneumocytoma demonstrating intratumoral hematoma.
Saxitoxin and neosaxitoxin as toxic principles of Alexandrium andersoni (Dinophyceae) from the Gulf of Naples, Italy.
Source and profile of paralytic shellfish poisoning toxins in shellfish in Daya Bay, South China Sea.
Termination of a toxic Alexandrium bloom with hydrogen peroxide.
Deglutition Disorders
A case of spinal anesthesia in a patient with progressive supranuclear palsy.
Case diagnosis and characterization of suspected paralytic shellfish poisoning in Alaska.
Clinical and neuropathologic features of progressive supranuclear palsy with severe pallido-nigro-luysial degeneration and axonal dystrophy.
Clinical Profile of Dysphagia in Patients with Parkinson's Disease, Progressive Supranuclear Palsy and Multiple System Atrophy.
Comparison of swallowing function in Parkinson's disease and progressive supranuclear palsy.
Cough reflex attenuation and swallowing dysfunction in sub-acute post-stroke patients: prevalence, risk factors, and clinical outcome.
Dysphagia in Progressive Supranuclear Palsy.
Dysphagia in progressive supranuclear palsy: radiologic features.
Endoscopic characteristics and levodopa responsiveness of swallowing function in progressive supranuclear palsy.
Eye movements and association with regional brain atrophy in clinical subtypes of progressive supranuclear palsy.
Freezing of gait is an early clinical feature of progressive supranuclear palsy.
Health-related quality of life in patients with progressive supranuclear palsy.
Low body weight in Parkinson's disease.
Natural clinical course of progressive supranuclear palsy in Chinese patients in Hong Kong.
Natural history of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) and clinical predictors of survival: a clinicopathological study.
Orofaryngeale slikstoornissen bij neurodegeneratieve aandoeningen.
Predictors of survival in progressive supranuclear palsy and multiple system atrophy: a systematic review and meta-analysis.
Progression of dysarthria and dysphagia in postmortem-confirmed parkinsonian disorders.
Risk factors for and impact of poststroke pneumonia in patients with acute ischemic stroke.
Usefulness of the Neutrophil-to-Lymphocyte Ratio as a Predictor of Pneumonia and Urinary Tract Infection Within the First Week After Acute Ischemic Stroke.
[A case of a syndrome resembling PSP after aortic arch replacement under deep hypothermic circulatory arrest].
[An assessment of dysphagia using videofluorography in Parkinson's disease and progressive supranuclear palsy]
Dehydration
Contribution of arbuscular mycorrhizal fungi and/or bacteria to enhancing plant drought tolerance under natural soil conditions: effectiveness of autochthonous or allochthonous strains.
Dementia
?-Synuclein in Plasma-Derived Extracellular Vesicles Is a Potential Biomarker of Parkinson's Disease.
A Novel MAPT Mutation, G55R, in a Frontotemporal Dementia Patient Leads to Altered Tau Function.
Accuracy of clinical criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome).
Accuracy of four clinical diagnostic criteria for the diagnosis of neurodegenerative dementias.
Alpha-synuclein Levels in the Differential Diagnosis of Lewy Bodies Dementia and Other Neurodegenerative Disorders: A Meta-analysis.
Anti-inflammatory drug use and progressive supranuclear palsy.
Apraxia of speech and nonfluent aphasia: a new clinical marker for corticobasal degeneration and progressive supranuclear palsy.
Argyrophilic grain disease is a sporadic 4-repeat tauopathy.
Argyrophilic grain disease: a late-onset dementia with distinctive features among tauopathies.
Basal ganglia cholinergic and dopaminergic function in progressive supranuclear palsy.
Behavior and cognition in corticobasal degeneration and progressive supranuclear palsy.
Brain dopamine transporter binding and glucose metabolism in progressive supranuclear palsy-like creutzfeldt-jakob disease.
Can the frontal assessment battery (FAB) differentiate bradykinetic rigid syndromes? Relation of the FAB to formal neuropsychological testing.
Cerebrospinal fluid levels of neurogranin in Parkinsonian disorders.
Characteristics and progression of cognitive deficits in progressive supranuclear palsy vs. multiple system atrophy and Parkinson's disease.
Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism.
Cholinergic cortical circuits in Parkinson's disease and in progressive supranuclear palsy: a transcranial magnetic stimulation study.
Clinical and genetic aspects of progressive supranuclear palsy.
Clinical genetics of familial progressive supranuclear palsy.
Clinical, MRI and 18F-FDG-PET/CT analysis of progressive supranuclear palsy.
Cognitive and behavioral aspects of PSP since Steele, Richardson and Olszewski's description of PSP 40 years ago and Albert's delineation of the subcortical dementia 30 years ago.
Cognitive disturbances in progressive supranuclear palsy.
Comparison of impaired subcortico-frontal metabolic networks in normal aging, subcortico-frontal dementia, and cortical frontal dementia.
Comparison of the pattern of atrophy of the corpus callosum in frontotemporal dementia, progressive supranuclear palsy, and Alzheimer's disease.
Concentration of neural thread protein in cerebrospinal fluid from progressive supranuclear palsy and Parkinson's disease.
Corticobasal ganglionic degeneration and progressive supranuclear palsy presenting with cognitive decline.
Critical appraisal of the role of davunetide in the treatment of progressive supranuclear palsy.
CSF sAPP? and sAPP? levels in Alzheimer's Disease and Multiple Other Neurodegenerative Diseases: A Network Meta-Analysis.
Development and assessment of sensitive immuno-PCR assays for the quantification of cerebrospinal fluid three- and four-repeat tau isoforms in tauopathies.
Diagnostic accuracy of progressive supranuclear palsy in the Society for Progressive Supranuclear Palsy brain bank.
Diagnostic Approach to Atypical Parkinsonian Syndromes.
Diagnostic potential of saccadometry in progressive supranuclear palsy.
Differentiation of PA from early PSP with different patterns of symptoms and CBF reduction.
Direct analysis of tau from PSP brain identifies new phosphorylation sites and a major fragment of N-terminally cleaved tau containing four microtubule-binding repeats.
Disease course and treatment patterns in progressive supranuclear palsy: A real-world study.
Early progressive supranuclear palsy: pathology and clinical presentation.
Early Stage of Progressive Supranuclear Palsy: A Neuropathological Study of 324 Consecutive Autopsy Cases.
Familial aggregation in atypical Parkinson's disease: a case control study in multiple system atrophy and progressive supranuclear palsy.
Familial aggregation in Progressive Supranuclear Palsy and Corticobasal Syndrome.
Familial aggregation of parkinsonism in progressive supranuclear palsy.
Follow-up study of risk factors in progressive supranuclear palsy.
Freezing of gait is an early clinical feature of progressive supranuclear palsy.
FTLD-TDP and progressive supranuclear palsy in comorbidity-a report of two cases with different clinical presentations.
Guadeloupean parkinsonism: a cluster of progressive supranuclear palsy-like tauopathy.
How to spot ocular abnormalities in progressive supranuclear palsy? A practical review.
In vivo retention of (18)F-AV-1451 in corticobasal syndrome.
Incipient progressive supranuclear palsy is more common than expected and may comprise clinicopathological subtypes: a forensic autopsy series.
It takes two to tango: carers' reflections on their participation and the participation of people with dementia in the James Lind Alliance process.
Late-onset Niemann-Pick disease type C overlapping with frontotemporal dementia syndromes: a case report.
Limb apraxia and cognitive impairment in progressive supranuclear palsy.
Long leukocyte telomere length at diagnosis is a risk factor for dementia progression in idiopathic parkinsonism.
Metabolic network expression in parkinsonism: Clinical and dopaminergic correlations.
Microtubule-associated protein tau genetic variations are uncommon cause of frontotemporal dementia in south India.
Mild Cognitive Impairment and Progression to Dementia in Progressive Supranuclear Palsy.
Motor, cognitive and behavioral differences in MDS PSP phenotypes.
Muscarinic receptors in the thalamus in progressive supranuclear palsy and other neurodegenerative disorders.
Mutations in bassoon in individuals with familial and sporadic progressive supranuclear palsy-like syndrome.
Natural history and predictors of survival in progressive supranuclear palsy.
Natural history of progressive supranuclear palsy: a clinicopathologic study from a population of brain donors.
Neuropathologic basis of frontotemporal dementia in progressive supranuclear palsy.
Neuropathological findings of PSP in the elderly without clinical PSP: Possible incidental PSP?
Neuropsychiatric assessment of patients with hyperkinetic and hypokinetic movement disorders.
Neuropsychiatric symptoms of progressive supranuclear palsy in a dementia clinic.
Obsessive-compulsive behavior as a symptom of dementia in progressive supranuclear palsy.
Orofaryngeale slikstoornissen bij neurodegeneratieve aandoeningen.
Patient and Public Involvement in Identifying Dementia Research Priorities.
Pattern of Tau forms in CSF is altered in progressive supranuclear palsy.
Phosphorylated TDP-43 pathology and hippocampal sclerosis in progressive supranuclear palsy.
Post mortem cerebrospinal fluid ?-synuclein levels are raised in multiple system atrophy and distinguish this from the other ?-synucleinopathies, Parkinson's disease and Dementia with Lewy bodies.
Progressive nonfluent aphasia and subsequent aphasic dementia associated with atypical progressive supranuclear palsy pathology.
Progressive Supranuclear Palsy and Statin Use.
Progressive supranuclear palsy combined with Alzheimer's disease: A clinicopathological study of two autopsy cases.
Progressive supranuclear palsy often develops idiopathic normal pressure hydrocephalus-like magnetic resonance imaging features.
Progressive supranuclear palsy on Guam.
Progressive supranuclear palsy with dementia: cortical pathology.
Progressive supranuclear palsy with fronto-temporal atrophy and various tau-positive abnormal structures.
Progressive supranuclear palsy.
Progressive supranuclear palsy: a clinicopathological study of 21 cases.
Progressive supranuclear palsy: clinico-pathological and biochemical studies.
Progressive Supranuclear Palsy: What do we know About it?
Psychiatric symptoms in progressive supranuclear palsy.
Quantitative proteomics identifies surfactant-resistant alpha-synuclein in cerebral cortex of parkinsonism-dementia complex of Guam but not alzheimer's disease or progressive supranuclear palsy.
Regional brain atrophy in progressive supranuclear palsy and Lewy body disease.
Rivastigmine for the treatment of dementia in patients with progressive supranuclear palsy: Clinical observations as a basis for power calculations and safety analysis.
Severity and specificity of cognitive impairment in Alzheimer's, Huntington's, and Parkinson's diseases and progressive supranuclear palsy.
Somatosensory evoked potentials in progressive supranuclear palsy.
Stimulation over the cerebellum with a regular figure-of-eight coil induces reduced motor cortex inhibition in patients with progressive supranuclear palsy.
Tau forms in CSF as a reliable biomarker for progressive supranuclear palsy.
Tau-Induced Pathology in Epilepsy and Dementia: Notions from Patients and Animal Models.
The basal ganglia cholinergic neurochemistry of progressive supranuclear palsy and other neurodegenerative diseases.
The Dementia Rating Scale in Alzheimer's disease, Huntington's disease and progressive supranuclear palsy.
The evolution and pathology of frontotemporal dementia.
The neuropsychological pattern of corticobasal degeneration: comparison with progressive supranuclear palsy and Alzheimer's disease.
Understanding the relationship between freezing of gait and other progressive supranuclear palsy features.
Visual event-related potentials in progressive supranuclear palsy.
Voxel-based morphometry in autopsy proven PSP and CBD.
Which clinical features differentiate progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) from related disorders? A clinicopathological study.
YKL-40: a novel prognostic fluid biomarker for preclinical Alzheimer's disease.
[A 57-year-old woman with progressive disturbance of gait and mental deterioration]
[A 85-year-old woman with the onset of progressive gait disturbance at 80 years of the age]
[An autopsy case of corticobasal degeneration without prominent cortical pathology--an imitator of progressive supranuclear palsy]
[Cerebral blood flow and oxygen metabolism in patients with pure akinesia and progressive supranuclear palsy]
[Corticobasal degeneration and atypical progressive supranuclear palsy: their symptomatology, laboratory examination and differential diagnosis]
[Event-related potentials in progressive supranuclear palsy]
[Palilalia associated with progressive supranuclear palsy]
[Progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): report of a case and review of the literature]
[Progressive supranuclear palsy with macular degeneration--report of three cases]
[Progressive supranuclear palsy]
[The thalamic changes in progressive supranuclear palsy]
Demyelinating Diseases
Abnormal signals on proton density-weighted MRI of the superior cerebellar peduncle in progressive supranuclear palsy.
Central hypoventilation in progressive supranuclear palsy.
Depression, Postpartum
Supporting women with perinatal mental health problems: the role of the voluntary sector.
Diabetes Mellitus
Antidiabetic activity of a polysaccharide-protein complex from Asian Clam (Corbicula fluminea) in streptozotoxin-induced diabetic rats and its underlying mechanism.
Black soybean tempeh and purple sweet potato improve sperm quality in streptozotocin-induced diabetic rats.
Clinical Features Observed in General Practice Associated With the Subsequent Diagnosis of Progressive Supranuclear Palsy.
Decreasing angiogenesis vasa vasorum through Lp-PLA2 and H2O2 inhibition by PSP from Ganoderma lucidum in atherosclerosis: in vivo diabetes mellitus type 2.
Optimizing insulin initiation in primary care: the Diabetes CoStars patient support program.
Polygonatum sibiricum polysaccharide potentially attenuates diabetic retinal injury in a diabetic rat model.
Serum pancreatic stone protein in pancreatic diseases.
Diabetes Mellitus, Type 2
Optimizing insulin initiation in primary care: the Diabetes CoStars patient support program.
Diabetic Nephropathies
Immunological characterization of pancreatic stone protein in human urine.
Urinary excretion of pancreatic stone protein in diabetic nephropathy.
Diabetic Retinopathy
Polygonatum sibiricum polysaccharide inhibits high glucose-induced oxidative stress, inflammatory response, and apoptosis in RPE cells.
Disorders of Excessive Somnolence
Sleep disturbances and brain MRI morphometry in Parkinson's disease, multiple system atrophy and progressive supranuclear palsy - a comparative study.
Drug-Related Side Effects and Adverse Reactions
Analysis of Pharmacology Data and the Prediction of Adverse Drug Reactions and Off-Target Effects from Chemical Structure.
Dry Eye Syndromes
Analysis of novel Sjogren's syndrome autoantibodies in patients with dry eyes.
Prevalence of Novel Candidate Sjögren Syndrome Autoantibodies in the Penn Sjögren's International Collaborative Clinical Alliance Cohort.
Dry Socket
Persistent socket pain postenucleation and post evisceration: a systematic review.
Duodenogastric Reflux
Comparative inhibition of coffee-induced gastric acid secretion employing misoprostol and cimetidine.
Dysarthria
A case of spinal anesthesia in a patient with progressive supranuclear palsy.
Acoustical Analysis of Speech in Progressive Supranuclear Palsy.
Case diagnosis and characterization of suspected paralytic shellfish poisoning in Alaska.
Clinical speech impairment in Parkinson's disease, progressive supranuclear palsy, and multiple system atrophy.
Differentiation of PA from early PSP with different patterns of symptoms and CBF reduction.
Distinct patterns of imprecise consonant articulation among Parkinson's disease, progressive supranuclear palsy and multiple system atrophy.
Early progressive supranuclear palsy: pathology and clinical presentation.
Effects of cerebellar neuromodulation in movement disorders: A systematic review.
Features of Patients With Nonfluent/Agrammatic Primary Progressive Aphasia With Underlying Progressive Supranuclear Palsy Pathology or Corticobasal Degeneration.
Freezing of gait is an early clinical feature of progressive supranuclear palsy.
Health-related quality of life in patients with progressive supranuclear palsy.
Low body weight in Parkinson's disease.
Major depressive disorder preceding the onset of progressive supranuclear palsy.
Motor Speech Disorders and Communication Limitations in Progressive Supranuclear Palsy.
Perceptual analysis of speech disorders in progressive supranuclear palsy.
Progression of dysarthria and dysphagia in postmortem-confirmed parkinsonian disorders.
Progressive Supranuclear Palsy: What do we know About it?
Speech disorders reflect differing pathophysiology in Parkinson's disease, progressive supranuclear palsy and multiple system atrophy.
Trial of Zolpidem, Eszopiclone, and Other GABA Agonists in a Patient with Progressive Supranuclear Palsy.
Dyskinesias
Comparison of motor, cognitive, and behavioral features in progressive supranuclear palsy and Parkinson's disease.
Dyskinesia in multiple system atrophy and progressive supranuclear palsy.
Effects of cerebellar neuromodulation in movement disorders: A systematic review.
Levodopa responsiveness in disorders with parkinsonism: a review of the literature.
Quantitative evaluation of oculomotor disturbances in progressive supranuclear palsy.
Dyspareunia
The clinical features and management of perineal endometriosis with anal sphincter involvement: a clinical analysis of 31 cases.
Dyspnea
Assessment of spontaneous pneumothorax in adults in a tertiary care hospital.
Bilateral primary spontaneous pneumothorax with multiple bleb performed by VATS and wedge resection: A rare case in Indonesian adult and review article.
Dystonia
Alternating flexed-extended posturing in progressive supranuclear palsy.
Botulinum toxin treatment in atypical parkinsonian disorders associated with disabling focal dystonia.
Clinical features differentiating patients with postmortem confirmed progressive supranuclear palsy and corticobasal degeneration.
Clinical features of dystonia in atypical parkinsonism.
Clinical genetics of familial progressive supranuclear palsy.
Comparison of dystonia between Parkinson's disease and atypical parkinsonism: The clinical usefulness of dystonia distribution and characteristics in the differential diagnosis of parkinsonism.
Dystonia in Parkinson's disease, multiple system atrophy, and progressive supranuclear palsy.
Dystonia in progressive supranuclear palsy.
Effects of cerebellar neuromodulation in movement disorders: A systematic review.
Laryngeal dystonia causing upper airway obstruction in progressive supranuclear palsy.
Levodopa-induced facial dystonia in a case of progressive supranuclear palsy.
Levodopa-induced oromandibular dystonia in progressive supranuclear palsy.
Limb dystonia in progressive supranuclear palsy.
Nocturnal manifestations of atypical and vascular parkinsonism: How do they differ from Parkinson's disease?
Progressive supranuclear palsy presenting with hyperkinetic movement disorder and hemiplegic dystonia: a case report.
Progressive supranuclear palsy with asymmetric tau pathology presenting with unilateral limb dystonia.
[A case of a syndrome resembling PSP after aortic arch replacement under deep hypothermic circulatory arrest].
[An assessment of dysphagia using videofluorography in Parkinson's disease and progressive supranuclear palsy]
[Dopaminergic drug-induced jaw-opening dystonia in a patient with progressive supranuclear palsy].
[Progressive supranuclear palsy: what's new?].
[Progressive supranuclear palsy]
[Widespread argentophilic structures in progressive supranuclear palsy--an autopsy case report]
Dystonic Disorders
Progressive supranuclear palsy: report of a case with torticollis, blepharospasm, and dysfluency.
Echolalia
Case Report: Barely Able to Speak, Can't Stop Echoing: Echolalic Dynamic Aphasia in Progressive Supranuclear Palsy.
Empyema
Pleural space problems after living lobar transplantation.
Encephalitis
Hashimoto's encephalopathy presenting as pseudobulbar palsy.
[A 85-year-old woman with the onset of progressive gait disturbance at 80 years of the age]
Encephalitis, Arbovirus
Progressive supranuclear palsy: new disease or variant of postencephalitic parkinsonism?
Endometrial Neoplasms
Membrane-associated serine/threonine protein phosphatase in endometrial cancer.
Epiretinal Membrane
Perisilicone proliferation after vitrectomy for proliferative vitreoretinopathy.
Erythema Infectiosum
Detection of IgE anti-parvovirus B19 and increased CD23+ B cells in parvovirus B19 infection: relation to Th2 cytokines.
Esophageal Achalasia
Full-layer mucosal histology in achalasia: Histological epithelial wave is characteristic in "pinstripe pattern"-positive achalasia.
Esophageal Neoplasms
A review of research on the protein-bound polysaccharide (polysaccharopeptide, PSP) from the mushroom Coriolus versicolor (Basidiomycetes: Polyporaceae).
The use of mushroom glucans and proteoglycans in cancer treatment.
Essential Tremor
Enlargements of somatosensory-evoked potentials in progressive supranuclear palsy.
Obsessive compulsive personality disorder in Progressive Supranuclear Palsy, Multiple System Atrophy and Essential Tremor.
The feasibility of statistical parametric mapping for the analysis of positron emission tomography studies using 11C-2-beta-carbomethoxy-3-beta-(4-fluorophenyl)-tropane in patients with movement disorders.
Tremor and longevity in relatives of patients with Parkinson's disease, essential tremor, and control subjects.
Exotropia
Exodeviated ophthalmoplegia in a patient with progressive supranuclear palsy.
Facial Nerve Injuries
Superficial parotidectomy versus retrograde partial superficial parotidectomy in treating benign salivary gland tumor (pleomorphic adenoma).
Febrile Neutropenia
Analyzing the capability of PSP, PCT and sCD25 to support the diagnosis of infection in cancer patients with febrile neutropenia.
Fecal Incontinence
The clinical features and management of perineal endometriosis with anal sphincter involvement: a clinical analysis of 31 cases.
Fetal Death
Perinatal and infant outcomes of prenatal diagnosis of heterotaxy syndrome (asplenia and polysplenia).
Foodborne Diseases
Measurements of paralytic shellfish poisons. A review of biological and chemical procedures.
Non-traditional vectors for paralytic shellfish poisoning.
Saxitoxin puffer fish poisoning in the United States, with the first report of Pyrodinium bahamense as the putative toxin source.
Simultaneous determination of twelve paralytic shellfish poisoning toxins in bivalve molluscs by UPLC-MS/MS and its applications to a food poisoning incident.
Foot Deformities
Joint and skeletal deformities in Parkinson's disease, multiple system atrophy, and progressive supranuclear palsy.
Frontotemporal Dementia
A combination of CSF tau ratio and midsaggital midbraintopons atrophy for the early diagnosis of progressive supranuclear palsy.
A Novel MAPT Mutation, G55R, in a Frontotemporal Dementia Patient Leads to Altered Tau Function.
Applause sign: is it really specific for Parkinsonian disorders? Evidence from cortical dementias.
Cognitive-behavioural features of progressive supranuclear palsy syndrome overlap with frontotemporal dementia.
Early and pre-symptomatic neuropsychological dysfunction in the PPND family with the N279K tau mutation.
Energization and spoken language production: Evidence from progressive supranuclear palsy.
Family history of frontotemporal lobar degeneration in Asia - an international multi-center research.
Frameshift proteins in autosomal dominant forms of Alzheimer disease and other tauopathies.
Frontotemporal lobar degeneration (FTLD) concept and classification update.
FTLD-TDP and progressive supranuclear palsy in comorbidity-a report of two cases with different clinical presentations.
Further extension of the H1 haplotype associated with progressive supranuclear palsy.
Increase in the relative expression of tau with four microtubule binding repeat regions in frontotemporal lobar degeneration and progressive supranuclear palsy brains.
Mild Cognitive Impairment and Progression to Dementia in Progressive Supranuclear Palsy.
Neurofibrillary tangle parkinsonian disorders--tau pathology and tau genetics.
Neuropathologic basis of frontotemporal dementia in progressive supranuclear palsy.
Neuropathology of variants of progressive supranuclear palsy.
Neuropsychiatric symptoms of progressive supranuclear palsy in a dementia clinic.
Oculomotor function in frontotemporal lobar degeneration, related disorders and Alzheimer's disease.
Parkinsonism plus syndrome--a review.
Pattern of Tau forms in CSF is altered in progressive supranuclear palsy.
Pin1 colocalization with phosphorylated tau in Alzheimer's disease and other tauopathies.
Polymorphisms in the tau gene in sporadic frontotemporal dementia and other neurodegenerative disorders.
Primary Tau Pathology, Not Copathology, Correlates With Clinical Symptoms in PSP and CBD.
Progressive supranuclear palsy presenting with hyperkinetic movement disorder and hemiplegic dystonia: a case report.
Relationship between frontotemporal dementia and corticobasal degeneration/progressive supranuclear palsy.
Sequence analysis of tau in familial and sporadic progressive supranuclear palsy.
Simulated brain biopsy for diagnosing neurodegeneration using autopsy-confirmed cases.
Staging disease severity in movement disorder tauopathies: brain atrophy separates progressive supranuclear palsy from corticobasal degeneration.
Stimulation over the cerebellum with a regular figure-of-eight coil induces reduced motor cortex inhibition in patients with progressive supranuclear palsy.
Strong association of a novel Tau promoter haplotype in progressive supranuclear palsy.
Tau exon 10 +16 mutation FTDP-17 presenting clinically as sporadic young onset PSP.
Tau forms in CSF as a reliable biomarker for progressive supranuclear palsy.
The Differential Diagnosis and Treatment of Atypical Parkinsonism.
The frontal assessment battery is not useful to discriminate progressive supranuclear palsy from frontotemporal dementias.
The tau gene in progressive supranuclear palsy: exclusion of mutations in coding exons and exon 10 splice sites, and identification of a new intronic variant of the disease-associated H1 haplotype in Italian cases.
Transglutaminase 1 and its regulator tazarotene-induced gene 3 localize to neuronal tau inclusions in tauopathies.
Untangling the tau gene association with neurodegenerative disorders.
[A clinical case of progressive supranuclear palsy with long-term frontal presentation preceding the onset of gaze palsy].
[Frontotemporal lobar degeneration (FTLD) - changes of its concept and classification based on aggregated proteins].
[Neurophysiology of corticobasal degeneration]
[Progressive nonfluent aphasia].
[The genetics of corticobasal syndrome].
Frontotemporal Lobar Degeneration
An autopsy case of frontotemporal lobar degeneration with the appearance of fused in sarcoma inclusions (basophilic inclusion body disease) clinically presenting corticobasal syndrome.
Analyses of the MAPT, PGRN, and C9orf72 mutations in Japanese patients with FTLD, PSP, and CBS.
Are frontotemporal lobar degeneration, progressive supranuclear palsy and corticobasal degeneration distinct diseases?
Biomarkers in frontotemporal lobar degenerations-Progress and challenges.
Caspase-cleaved tau accumulation in neurodegenerative diseases associated with tau and alpha-synuclein pathology.
Clinicopathologic analysis of frontotemporal and corticobasal degenerations and PSP.
Detection of Alzheimer Disease (AD)-Specific Tau Pathology in AD and NonAD Tauopathies by Immunohistochemistry With Novel Conformation-Selective Tau Antibodies.
Detection of Alzheimer's disease (AD) specific tau pathology with conformation-selective anti-tau monoclonal antibody in co-morbid frontotemporal lobar degeneration-tau (FTLD-tau).
First symptom guides diagnosis and prognosis in neurodegenerative diseases-a retrospective study of autopsy proven cases.
Frontotemporal lobar degeneration (FTLD) concept and classification update.
Genetic pleiotropy and the shared pathological features of corticobasal degeneration and progressive supranuclear palsy: a case report and a review of the literature.
Genetics of Progressive Supranuclear Palsy.
High-Contrast In Vivo Imaging of Tau Pathologies in Alzheimer's and Non-Alzheimer's Disease Tauopathies.
Increase in the relative expression of tau with four microtubule binding repeat regions in frontotemporal lobar degeneration and progressive supranuclear palsy brains.
Integrative system biology analyses of CRISPR-edited iPSC-derived neurons and human brains reveal deficiencies of presynaptic signaling in FTLD and PSP.
Level of PICALM, a key component of clathrin-mediated endocytosis, is correlated with levels of phosphotau and autophagy-related proteins and is associated with tau inclusions in AD, PSP and Pick disease.
New insights into biological markers of frontotemporal lobar degeneration spectrum.
Niemann-Pick C disease gene mutations and age-related neurodegenerative disorders.
Non-Alzheimer's disease dementias: anatomic, clinical, and molecular correlates.
Oculomotor function in frontotemporal lobar degeneration, related disorders and Alzheimer's disease.
Progressive modulation of the human olfactory bulb transcriptome during Alzheimer´s disease evolution: novel insights into the olfactory signaling across proteinopathies.
Seizure prevalence in neurodegenerative diseases-a study of autopsy proven cases.
Sensitivity-Specificity of Tau and Amyloid ? Positron Emission Tomography in Frontotemporal Lobar Degeneration.
The olfactory bulb proteotype differs across frontotemporal dementia spectrum.
[Frontotemporal lobar degeneration (FTLD) - changes of its concept and classification based on aggregated proteins].
Gallstones
Serum pancreatic stone protein in pancreatic diseases.
Ganglioglioma
Ki-67 immunoreactivity in Alzheimer's disease and other neurodegenerative disorders.
Gaucher Disease
Central ocular motor disorders, including gaze palsy and nystagmus.
Glioblastoma
219?Liquid Biopsy Can Distinguish Recurrent Glioblastomas From Pseudoprogression and Radiation Necrosis After Concurrent Radiochemotherapy.
A Preliminary Study on Machine Learning-Based Evaluation of Static and Dynamic FET-PET for the Detection of Pseudoprogression in Patients with IDH-Wildtype Glioblastoma.
Can Tumor Location on Pre-treatment MRI Predict Likelihood of Pseudo-Progression vs. Tumor Recurrence in Glioblastoma?-A Feasibility Study.
Combined analysis of MGMT methylation and dynamic-susceptibility-contrast MRI for the distinction between early and pseudo-progression in glioblastoma patients.
Diagnosis of pseudoprogression in patients with glioblastoma using O-(2-[(18)F]fluoroethyl)-L-tyrosine PET.
Histopathology-validated machine learning radiographic biomarker for noninvasive discrimination between true progression and pseudo-progression in glioblastoma.
Low incidence of pseudoprogression by imaging in newly diagnosed glioblastoma patients treated with cediranib in combination with chemoradiation.
Pseudoprogression as an adverse event of glioblastoma therapy.
Serine/threonine protein phosphatase 6 modulates the radiation sensitivity of glioblastoma.
Systemic siRNA delivery to tumors by cell-penetrating ?-helical polypeptide-based metastable nanoparticles.
Glioma
Analysis of pseudoprogression after proton or photon therapy of 99 patients with low grade and anaplastic glioma.
Central ocular motor disorders, including gaze palsy and nystagmus.
Differentiating high-grade glioma recurrence from pseudoprogression: Comparing diffusion kurtosis imaging and diffusion tensor imaging.
Evaluation of polysaccharopeptide effects against C6 glioma in combination with radiation.
Increase of pseudoprogression and other treatment related effects in low-grade glioma patients treated with proton radiation and temozolomide.
Meta-analysis of the diagnostic performance of diffusion magnetic resonance imaging with apparent diffusion coefficient measurements for differentiating glioma recurrence from pseudoprogression.
Pseudoprogression in children, adolescents and young adults with non-brainstem high grade glioma and diffuse intrinsic pontine glioma.
Pseudoprogression: Patient experience and nursing in uncertainty.
The value of MGMT promote methylation and IDH-1 mutation on diagnosis of pseudoprogression in patients with high-grade glioma: A meta-analysis.
Hallucinations
Atypical parkinsonism in Guadeloupe: a common risk factor for two closely related phenotypes?
Hydrocephalic Parkinsonism: lessons from normal pressure hydrocephalus mimics.
Photophobia, visual hallucinations, and REM sleep behavior disorder in progressive supranuclear palsy and corticobasal degeneration: A prospective study.
Predominant cortical dysfunction in Guadeloupean parkinsonism.
Progressive supranuclear palsy, multiple system atrophy and corticobasal degeneration.
Heart Failure
Four and a half LIM domain protein signaling and cardiomyopathy.
HELLP Syndrome
[Hepatic Rupture as a Complication of Hypertensive Disease of Pregnancy Maternal and the HELLP Syndrome]
Hemangiosarcoma
Single agent polysaccharopeptide delays metastases and improves survival in naturally occurring hemangiosarcoma.
Hematuria
In vitro immunoglobulin production by peripheral blood mononuclear cells as a prognostic factor in IgA nephropathy.
Renal glomerular changes associated with liver cirrhosis.
Hemorrhagic Stroke
Vascular Parkinsonism: deconstructing a syndrome.
Hemothorax
The effect of pleural abrasion on the treatment of primary spontaneous pneumothorax: a systematic review of randomized controlled trials.
Hepatitis
Intake of purple sweet potato beverage affects on serum hepatic biomarker levels of healthy adult men with borderline hepatitis.
Preclinical and clinical studies of Coriolus versicolor polysaccharopeptide as an immunotherapeutic in China.
Herpes Simplex
Detection of herpes simplex virus and adenovirus DNA by dot blot hybridization using in vitro synthesized RNA transcripts.
Herpes Zoster
Aggregated and monomeric forms of proteins in boar seminal plasma: characterization and binding properties.
Sperm surface proteins in mammalian fertilization.
Hidradenitis
Patient Support Program Increased Medication Adherence with Lower Total Health Care Costs Despite Increased Drug Spending.
HIV Infections
Reversible progressive supranuclear palsy-like phenotype as an initial manifestation of HIV infection.
Huntington Disease
Applause sign in Parkinsonian disorders and Huntington's disease.
Pathologic correlates of supranuclear gaze palsy with parkinsonism.
Polymorphisms in the tau gene in sporadic frontotemporal dementia and other neurodegenerative disorders.
The Dementia Rating Scale in Alzheimer's disease, Huntington's disease and progressive supranuclear palsy.
Hydrocephalus
Hydrocephalic Parkinsonism: lessons from normal pressure hydrocephalus mimics.
Magnetic Resonance Imaging Biomarkers Distinguish Normal Pressure Hydrocephalus From Progressive Supranuclear Palsy.
Parkinsonian syndromes associated with hydrocephalus: case reports, a review of the literature, and pathophysiological hypotheses.
Progressive supranuclear palsy often develops idiopathic normal pressure hydrocephalus-like magnetic resonance imaging features.
The in vitro evaluation of the PSP and indigo carmine tests for obstruction in hydrocephalus.
Vascular Parkinsonism: deconstructing a syndrome.
[Cerebrospinal fluid absorption mechanism--based on measurement of CSF flow rate in shunt tube]
Hydrocephalus, Normal Pressure
Hydrocephalic Parkinsonism: lessons from normal pressure hydrocephalus mimics.
Magnetic Resonance Imaging Biomarkers Distinguish Normal Pressure Hydrocephalus From Progressive Supranuclear Palsy.
Hyperalgesia
Subcutaneous ?-Conotoxins Alleviate Mechanical Pain in Rodent Models of Acute Peripheral Neuropathy.
Hyperemia
Peripheral arterial endothelial dysfunction of neurodegenerative diseases.
Hyperglycemia
Seed Proteomic Profiles of Three Paeonia Varieties and Evaluation of Peony Seed Protein as a Food Product.
Hyperhidrosis
Characterisation of pleural inflammation occurring after primary spontaneous pneumothorax.
Hyperkinesis
Neuropsychiatric assessment of Gilles de la Tourette patients: comparative study with other hyperkinetic and hypokinetic movement disorders.
Progressive supranuclear palsy presenting with hyperkinetic movement disorder and hemiplegic dystonia: a case report.
Hyperlipidemias
Coriolus versicolor polysaccharopeptide as an immunotherapeutic in China.
Preclinical and clinical studies of Coriolus versicolor polysaccharopeptide as an immunotherapeutic in China.
[Effect of polysaccharides from Polygonatum sibiricum on lipid-metabolism related mRNA and protein expression in hyperlipidemic mice].
Hypersensitivity
Corrigendum.
Dietary supplementation with mushroom-derived protein-bound glucan does not enhance immune function in young and old mice.
Immune enhancement of a polysaccharides peptides isolated from Coriolus versicolor.
Patient engagement and patient support programs in allergy immunotherapy: a call to action for improving long-term adherence.
Use of the biventer cervicis nerve-muscle preparation to detect early changes following exposure to organophosphates inducing delayed neuropathy.
Hypertension
Cause, seasonality of death and co-morbidities in progressive supranuclear palsy (PSP).
Environmental Risk Factors for Progressive Supranuclear Palsy.
Hypertension and progressive supranuclear palsy.
In vitro immunoglobulin production by peripheral blood mononuclear cells as a prognostic factor in IgA nephropathy.
Relationship between postoperative blood pressure change and renal pathophysiology in primary aldosteronism.
Renal function studies in hypertension: with particular reference to the intravenous PSP test.
Risk factors for progressive supranuclear palsy.
[Incidence, etiology and prognostic value of persistent significant proteinuria in kidney transplants]
Hypesthesia
Hypodipsia discriminates progressive supranuclear palsy from other parkinsonian syndromes.
Hypokinesia
Application of the Unified Parkinson's Disease Rating Scale in progressive supranuclear palsy: factor analysis of the motor scale.
Assessing bradykinesia in parkinsonian disorders.
Brain regional iron contents in progressive supranuclear palsy.
Clinical and dual-tasking aspects in frequent and infrequent fallers with progressive supranuclear palsy.
Coexistence of Progressive Supranuclear Palsy With Pontocerebellar Atrophy and Myotonic Dystrophy Type 1.
Comparison of natural histories of progressive supranuclear palsy and multiple system atrophy.
Facial bradykinesia.
Increased tau burden in the cortices of progressive supranuclear palsy presenting with corticobasal syndrome.
Laboratory based assessment of gait and balance impairment in patients with progressive supranuclear palsy.
Motor function in Parkinson's disease and supranuclear palsy: simultaneous factor analysis of a clinical scale in several populations.
Natural history and clinical features of progressive supranuclear palsy: a clinical study.
Parkinson's syndrome associated with neurofibrillary degeneration and tau pathologic findings.
Progressive Supranuclear Palsy and Corticobasal Degeneration: Pathophysiology and Treatment Options.
Progressive supranuclear palsy.
The evolution of parkinsonism in primary progressive apraxia of speech: A 6-year longitudinal study.
Which clinical features differentiate progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) from related disorders? A clinicopathological study.
[An autopsy case of corticobasal degeneration without prominent cortical pathology--an imitator of progressive supranuclear palsy]
[Progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): report of a case and review of the literature]
Hypotension, Orthostatic
Physiological, pharmacological and neurohormonal assessment of autonomic function in progressive supranuclear palsy.
Progressive supranuclear palsy is not associated with neurogenic orthostatic hypotension.
Unusual phenotype of pathologically confirmed progressive supranuclear palsy with autonomic dysfunction and cerebellar ataxia: Case report.
Hypothyroidism
Adult-onset hypothyroidism impairs paired-pulse facilitation and long-term potentiation of the rat dorsal hippocampo-medial prefrontal cortex pathway in vivo.
Hypoventilation
Central hypoventilation in progressive supranuclear palsy.
Ichthyosis, Lamellar
The pathogenesis of severe congenital ichthyosis of the neonate.
Immune System Diseases
Patient engagement and patient support programs in allergy immunotherapy: a call to action for improving long-term adherence.
Infections
A phagemid vector using the E. coli phage shock promoter facilitates phage display of toxic proteins.
A validation of presepsin levels in kidney dysfunction patients: four case reports.
Accuracy of pancreatic stone protein for the diagnosis of infection in hospitalized adults: a systematic review and individual patient level meta-analysis.
Analysis of the proteins and cis-acting elements regulating the stress-induced phage shock protein operon.
Analyzing the capability of PSP, PCT and sCD25 to support the diagnosis of infection in cancer patients with febrile neutropenia.
Cerebrospinal Fluid Presepsin As a Marker of Nosocomial Infections of the Central Nervous System: A Prospective Observational Study.
Clinical application of presepsin as diagnostic biomarker of infection: overview and updates.
Detection of IgE anti-parvovirus B19 and increased CD23+ B cells in parvovirus B19 infection: relation to Th2 cytokines.
Effect of the endoparasite Amoebophrya sp. on toxin content and composition in the paralytic shellfish poisoning dinoflagellate Alexandrium fundyense (Dinophyceae).
Evaluating the Role of Phage-Shock Protein A in Burkholderia pseudomallei.
Identification of 3-acyl-2-phenylamino-1,4-dihydroquinolin-4-one derivatives as inhibitors of the phosphatase SerB653 in Porphyromonas gingivalis, implicated in periodontitis.
Leishmania donovani secretory serine protease alters macrophage inflammatory response via COX-2 mediated PGE-2 production.
Pancreatic stone protein and soluble CD25 for infection and sepsis in an emergency department.
Pancreatic stone protein as a novel marker for neonatal sepsis.
Pancreatic stone protein predicts postoperative infection in cardiac surgery patients irrespective of cardiopulmonary bypass or surgical technique.
Pancreatic Stone Protein Predicts Sepsis in Severely Burned Patients Irrespective of Trauma Severity: A Monocentric Observational Study.
Pneumonia caused by penicillin-non-susceptible and penicillin-susceptible pneumococci in adults: a case-control study.
Polysaccharide peptide from Coriolus versicolor induces interleukin 6-related extension of endotoxin fever in rats.
Presepsin in risk stratification of SARS-CoV-2 patients.
Prognostic value of flow cytometry in surgically treated primary gastric lymphoma.
Prognostic value of sCD14-ST (presepsin) in cardiac surgery.
Propagation of prions causing synucleinopathies in cultured cells.
Pseudomonas peritonitis in peritoneal dialysis patients: the Network #9 Peritonitis Study.
PSP and NT-proCNP assessed for predisposition to infection.
Regulation of the phage-shock-protein stress response in Yersinia enterocolitica.
Respiratory virus associated with surgery in children patients.
Risk factors for and impact of poststroke pneumonia in patients with acute ischemic stroke.
Stress-induced expression of the Escherichia coli phage shock protein operon is dependent on sigma 54 and modulated by positive and negative feedback mechanisms.
The phage-shock-protein response.
The value of pancreatic stone protein in predicting acute appendicitis in patients presenting at the emergency department with abdominal pain.
Understanding the Impact of Drought on Foliar and Xylem Invading Bacterial Pathogen Stress in Chickpea.
vRNA structured population model for Hepatitis C Virus dynamics.
[Inflammation markers and bloodstream infection (review of literature).]
Influenza, Human
Heterogeneous selective pressure acting on influenza B victoria- and yamagata-like hemagglutinins.
Insulin Resistance
Effects of calcineurin activation on insulin-, AICAR- and contraction-induced glucose transport in skeletal muscle.
Intellectual Disability
On the phenotypic spectrum of serine biosynthesis defects.
Phosphoserine phosphatase (PSPH) gene mutation in an intellectual disability family from Pakistan.
Profile of children with poor school performance in Mumbai.
Ischemic Stroke
Post-stroke pneumonia at the stroke unit - a registry based analysis of contributing and protective factors.
Reduction of Neuromelanin-Positive Nigral Volume in Patients with MSA, PSP and CBD.
Risk factors for and impact of poststroke pneumonia in patients with acute ischemic stroke.
Risk stratification model for post-stroke pneumonia in patients with acute ischemic stroke.
[Vascular Wallerian degeneration on magnetic resonance in a patient with probable progressive supranuclear palsy: aetiology or casual link?]
Kernicterus
Serum albumin reserve PSP dye binding capacity in infants with kernicterus.
Kidney Failure, Chronic
Serum pancreatic stone protein in pancreatic diseases.
Kidney Neoplasms
A 4-bp deletion in the Birt-Hogg-Dubé gene (FLCN) causes dominantly inherited spontaneous pneumothorax.
Novel in-frame deletion mutation in FLCN gene in a Korean family with recurrent primary spontaneous pneumothorax.
Language Disorders
Behavior and cognition in corticobasal degeneration and progressive supranuclear palsy.
Language Disorder in Progressive Supranuclear Palsy and Corticobasal Syndrome: Neural Correlates and Detection by the MLSE Screening Tool.
Learning Disabilities
Profile of children with poor school performance in Mumbai.
Leishmaniasis, Visceral
Leishmania donovani secretory serine protease alters macrophage inflammatory response via COX-2 mediated PGE-2 production.
Leukemia
A comparison of races and leukemia subtypes among patients in different cancer survivorship phases.
Augmentation of retinoic acid-induced granulocytic differentiation in HL-60 leukemia cells by serine/threonine protein phosphatase inhibitors.
Gossypol exerts its cytotoxic effect on HL-60 leukemic cell line via decreasing activity of protein phosphatase 2A and interacting with human telomerase reverse transcriptase activity.
Induction of S phase cell arrest and caspase activation by polysaccharide peptide isolated from Coriolus versicolor enhanced the cell cycle dependent activity and apoptotic cell death of doxorubicin and etoposide, but not cytarabine in HL-60 cells.
Polysaccharopeptide enhances the anticancer activity of doxorubicin and etoposide on human breast cancer cells ZR-75-30.
Polysaccharopeptides derived from Coriolus versicolor potentiate the S-phase specific cytotoxicity of Camptothecin (CPT) on human leukemia HL-60 cells.
The anti-tumor effect of a small polypeptide from Coriolus versicolor (SPCV).
The cell death process of the anticancer agent polysaccharide-peptide (PSP) in human promyelocytic leukemic HL-60 cells.
Leukemia, Lymphocytic, Chronic, B-Cell
Trisomy 12 in chronic lymphocytic leukemia: an interphase cytogenetic study.
Leukemia, Myeloid
Augmentation of methylprednisolone-induced differentiation of myeloid leukemia cells by serine/threonine protein phosphatase inhibitors.
Leukemia, T-Cell
Progressive spastic paraparesis associated with human T-cell leukemia virus type I (HTLV-I).
Leukocytosis
Progressive spastic paraparesis associated with human T-cell leukemia virus type I (HTLV-I).
Lewy Body Disease
Accuracy of clinical criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome).
An autopsy case of frontotemporal lobar degeneration with the appearance of fused in sarcoma inclusions (basophilic inclusion body disease) clinically presenting corticobasal syndrome.
Brain dopamine transporter binding and glucose metabolism in progressive supranuclear palsy-like creutzfeldt-jakob disease.
Cerebral peduncle angle: Unreliable in differentiating progressive supranuclear palsy from other neurodegenerative diseases.
Level of PICALM, a key component of clathrin-mediated endocytosis, is correlated with levels of phosphotau and autophagy-related proteins and is associated with tau inclusions in AD, PSP and Pick disease.
Lewy bodies in progressive supranuclear palsy.
Neurofibrillary tangles in the dentate granule cells of patients with Alzheimer's disease, Lewy body disease and progressive supranuclear palsy.
Predicting alpha-synuclein pathology by REM sleep behavior disorder diagnosis.
Progressive supranuclear palsy is not associated with neurogenic orthostatic hypotension.
Regional brain atrophy in progressive supranuclear palsy and Lewy body disease.
Susceptibility MRI captures nigral pathology in patients with parkinsonian syndromes.
Tau pathology in the olfactory bulb correlates with Braak stage, Lewy body pathology and apolipoprotein epsilon4.
Which clinical features differentiate progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) from related disorders? A clinicopathological study.
Liver Cirrhosis
Assessing the permeability of the gastrointestinal mucosa after oral administration of phenolsulfonphthalein.
Serum pancreatic stone protein in pancreatic diseases.
Liver Diseases
Diagnostic and prognostic role of presepsin in patients with cirrhosis and bacterial infection.
Influence of liver disease on phenolsulfonphthalein absorption from liver surface to examine possibility of direct liver surface application for drug targeting.
Proteoglycan isolated from Corbicula fluminea exerts hepato-protective effects against alcohol-induced liver injury in mice.
Significance of the peroral phenolsulfonphthalein test in hepatic resection: a possible predictor of bacterial translocation.
Liver Neoplasms
Enhancing the utility of Proteomics Signature Profiling (PSP) with Pathway Derived Subnets (PDSs), performance analysis and specialised ontologies.
Lordosis
Induction of pseudopregnancy using artificial VCS: importance of lordosis intensity and prestimulus estrous cycle length.
Lung Diseases
A 4-bp deletion in the Birt-Hogg-Dubé gene (FLCN) causes dominantly inherited spontaneous pneumothorax.
A biomechanical hypothesis for the pathophysiology of apical lung disease.
Unilateral single-port thoracoscopic surgery for bilateral pneumothorax or pulmonary bullae.
[Management of pneumothorax]
Lung Neoplasms
A review of research on the protein-bound polysaccharide (polysaccharopeptide, PSP) from the mushroom Coriolus versicolor (Basidiomycetes: Polyporaceae).
Analysis of the clinical differentiation of pulmonary sclerosing pneumocytoma and lung cancer.
Immunomodulatory effects of herbal formula of astragalus polysaccharide (APS) and polysaccharopeptide (PSP) in mice with lung cancer.
Large pulmonary sclerosing pneumocytoma with massive necrosis and vascular invasion: a case report.
Phosphoserine Phosphatase Promotes Lung Cancer Progression through the Dephosphorylation of IRS-1 and a Noncanonical L-Serine-Independent Pathway.
Polygonatum sibiricum polysaccharides play anti-cancer effect through TLR4-MAPK/NF-?B signaling pathways.
Pulmonary sclerosing pneumocytoma mimicking lung cancer: Case report and review of the literature.
Relevance of the rat lung tumor response to particle overload for human risk assessment-Update and interpretation of new data since ILSI 2000.
RHOB expression controls the activity of serine/threonine protein phosphatase PP2A to modulate mesenchymal phenotype and invasion in non-small cell lung cancers.
Toxicokinetics and effects of fibrous and nonfibrous particles.
Upregulation of phosphoserine phosphatase contributes to tumor progression and predicts poor prognosis in non-small cell lung cancer patients.
Lymphatic Metastasis
Clinical and histopathologic features of pulmonary sclerosing pneumocytoma with dense spindle stromal cells and lymph node metastasis.
Large pulmonary sclerosing pneumocytoma with massive necrosis and vascular invasion: a case report.
Pulmonary sclerosing pneumocytoma with mediastinal lymph node metastasis: a case report.
[Resection of gastric carcinoma with preserving of the spleen and pancreas and functional clearance lymph nodes of the spleen hillus and splenic artery]
Lymphoma
Protective effect of polysaccharide peptide on cerebral ischemia?reperfusion injury in rats.
Lymphoma, B-Cell
Paraneoplastic progressive supranuclear palsy syndrome in a patient with B-cell lymphoma.
Machado-Joseph Disease
Hypertrophy of the inferior olivary nucleus in patients with progressive supranuclear palsy.
Macular Degeneration
Impact of a Patient Support Program on Patient Beliefs About Neovascular Age-Related Macular Degeneration and Persistence to Anti-Vascular Endothelial Growth Factor Therapy.
[Progressive supranuclear palsy with macular degeneration--report of three cases]
Malaria
A novel tetratricopeptide repeat (TPR) containing PP5 serine/threonine protein phosphatase in the malaria parasite, Plasmodium falciparum.
Characterisation and expression of a PP1 serine/threonine protein phosphatase (PfPP1) from the malaria parasite, Plasmodium falciparum: demonstration of its essential role using RNA interference.
Characterization of a novel serine/threonine protein phosphatase (PfPPJ) from the malaria parasite, Plasmodium falciparum.
Mania
Self-Reported Graphic Personal and Social Performance Scale (SRG-PSP) for measuring functionality in patients with bipolar disorder.
Melanoma
PSPH promotes melanoma growth and metastasis by metabolic deregulation-mediated transcriptional activation of NR4A1.
Memory Disorders
Heterogeneity of cognitive impairment in progressive supranuclear palsy, Parkinson's disease, and Alzheimer's disease.
Mesothelioma
Enzyme pathology of human mesotheliomas.
Migraine Disorders
Menstrual migraine: a possible pathogenic implication of platelet function.
Miller Fisher Syndrome
[Clinical analysis of paralytic shellfish poisoning following ingestion of oysters]
Motor Neuron Disease
Family history of frontotemporal lobar degeneration in Asia - an international multi-center research.
Hashimoto's encephalopathy presenting as pseudobulbar palsy.
Possible relation of atypical parkinsonism in the French West Indies with consumption of tropical plants: a case-control study. Caribbean Parkinsonism Study Group.
Progressive supranuclear palsy (PSP): Richardson syndrome and other PSP variants.
Progressive supranuclear palsy presenting as primary lateral sclerosis but lacking parkinsonism, gaze palsy, aphasia, or dementia.
Relationship between frontotemporal dementia and corticobasal degeneration/progressive supranuclear palsy.
The analysis of C9orf72 repeat expansions in a large series of clinically and pathologically diagnosed cases with atypical parkinsonism.
Movement Disorders
Advances in progressive supranuclear palsy: new diagnostic criteria, biomarkers, and therapeutic approaches.
An Evaluation of the Progressive Supranuclear Palsy Speech/Language Variant.
Are the International Parkinson disease and Movement Disorder Society progressive supranuclear palsy (IPMDS-PSP) diagnostic criteria accurate enough to differentiate common PSP phenotypes?
Assessment of 18F-PI-2620 as a Biomarker in Progressive Supranuclear Palsy.
Association of Tripartite Motif Containing 11 rs564309 with Tau Pathology in Progressive Supranuclear Palsy.
Cerebellar involvement in progressive supranuclear palsy: A clinicopathological study.
Clinical Correlation Between Vertical Gaze Palsy and Midbrain Volume in Progressive Supranuclear Palsy.
Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria.
Clinical Milestones Preceding the Diagnosis of Multiple System Atrophy and Progressive Supranuclear Palsy: A Retrospective Cohort Study.
Clinimetric Analysis of the Motor Section of the Progressive Supranuclear Palsy Rating Scale: Reliability and Factor Analysis.
Development and Validation of the Automated Imaging Differentiation in Parkinsonism (AID-P): A Multi-Site Machine Learning Study.
Diagnosis Across the Spectrum of Progressive Supranuclear Palsy and Corticobasal Syndrome.
Disease course and treatment patterns in progressive supranuclear palsy: A real-world study.
Effect of aging on magnetic resonance measures differentiating progressive supranuclear palsy from Parkinson's disease.
Enlargements of somatosensory-evoked potentials in progressive supranuclear palsy.
Environmental and Occupational Risk Factors for Progressive Supranuclear Palsy: Case-Control Study.
Free water improves detection of changes in the substantia nigra in parkinsonism: A multisite study.
Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study.
Genome-wide survey of copy number variants finds MAPT duplications in progressive supranuclear palsy.
Glucose metabolic brain patterns to discriminate amyotrophic lateral sclerosis from Parkinson plus syndromes.
Hypodipsia discriminates progressive supranuclear palsy from other parkinsonian syndromes.
In vivo comparison of Richardson's syndrome and progressive supranuclear palsy-parkinsonism.
Is the Latency from Progressive Supranuclear Palsy Onset to Diagnosis Improving?
Joint and skeletal deformities in Parkinson's disease, multiple system atrophy, and progressive supranuclear palsy.
Long lasting pure freezing of gait preceding progressive supranuclear palsy: A clinicopathological study.
Longitudinal magnetic resonance imaging in progressive supranuclear palsy: A new combined score for clinical trials.
Manual MRI morphometry in Parkinsonian syndromes.
Midbrain MRI assessments in progressive supranuclear palsy subtypes.
Midbrain/pons area ratio and clinical features predict the prognosis of progressive Supranuclear palsy.
MRI Outperforms [18F]AV-1451 PET as a Longitudinal Biomarker in Progressive Supranuclear Palsy.
Multimodal Magnetic Resonance Imaging Quantification of Brain Changes in Progressive Supranuclear Palsy.
Neuromelanin imaging and midbrain volumetry in progressive supranuclear palsy and Parkinson's disease.
Neuropathological findings of PSP in the elderly without clinical PSP: Possible incidental PSP?
Neuropsychiatric assessment of Gilles de la Tourette patients: comparative study with other hyperkinetic and hypokinetic movement disorders.
Neuropsychiatric symptoms of progressive supranuclear palsy in a dementia clinic.
Olfaction in Neuropathologically Defined Progressive Supranuclear Palsy.
One decade ago, one decade ahead in progressive supranuclear palsy.
Patient and care partner views on exercise and structured physical activity for people with Progressive Supranuclear Palsy.
PET measurement of cardiac and nigrostriatal denervation in Parkinsonian syndromes.
Preclinical, Phase I, and phase II investigational clinical trials for treatment of progressive supranuclear palsy.
Progression of gait, speech and swallowing deficits in progressive supranuclear palsy.
Progressive supranuclear palsy and idiopathic Parkinson's disease are associated with local reduction of in vivo brain viscoelasticity.
Progressive supranuclear palsy presenting with hyperkinetic movement disorder and hemiplegic dystonia: a case report.
Progressive Supranuclear Palsy: an Update.
Psychometric properties of the Beck Depression Inventory-II in progressive supranuclear palsy.
Pyramidal system involvement in progressive supranuclear palsy - a clinicopathological correlation.
Sensitivity and Specificity of Diagnostic Criteria for Progressive Supranuclear Palsy.
Study of LRRK2 variation in tauopathy: Progressive supranuclear palsy and corticobasal degeneration.
Subtypes of PSP and Prognosis: A Retrospective Analysis.
Thalamic stimulation-evoked sensations in chronic pain patients and in nonpain (movement disorder) patients.
The diagnosis of progressive supranuclear palsy: current opinions and challenges.
The feasibility of statistical parametric mapping for the analysis of positron emission tomography studies using 11C-2-beta-carbomethoxy-3-beta-(4-fluorophenyl)-tropane in patients with movement disorders.
The language profile of progressive supranuclear palsy.
The tau positron-emission tomography tracer AV-1451 binds with similar affinities to tau fibrils and monoamine oxidases.
Tideglusib reduces progression of brain atrophy in progressive supranuclear palsy in a randomized trial.
Validation of the Italian version of carers' quality-of-life questionnaire for parkinsonism (PQoL Carer) in progressive supranuclear palsy.
Validation of the Italian version of the PSP Quality of Life questionnaire.
Multiple System Atrophy
A novel diagnostic marker for progressive supranuclear palsy targeting atrophy of the subthalamic nucleus.
Accuracy of clinical criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome).
Amantadine-induced myoclonus in a patient with progressive supranuclear palsy.
Applause sign in Parkinsonian disorders and Huntington's disease.
Association of PSP phenotypes with survival: A brain-bank study.
Automated Brainstem Segmentation Detects Differential Involvement in Atypical Parkinsonian Syndromes.
Blood-based NfL: A biomarker for differential diagnosis of parkinsonian disorder.
Botulinum toxin treatment in atypical parkinsonian disorders associated with disabling focal dystonia.
Can the frontal assessment battery (FAB) differentiate bradykinetic rigid syndromes? Relation of the FAB to formal neuropsychological testing.
Central nystagmus in progressive supranuclear palsy: A neglected clinical feature?
Clinical analysis of blepharospasm and apraxia of eyelid opening in patients with parkinsonism.
Coexistence of PSP and MSA: a case report and review of the literature.
Cognitive dysfunction and impaired organization of complex motility in degenerative parkinsonian syndromes.
Combination of dopamine transporter and D2 receptor SPECT in the diagnostic evaluation of PD, MSA, and PSP.
Conventional magnetic resonance imaging in confirmed progressive supranuclear palsy and multiple system atrophy.
Diagnostic accuracy of MR planimetry in clinically unclassifiable parkinsonism.
Differentiating PSP from MSA using MR planimetric measurements: a systematic review and meta-analysis.
Direct genetic evidence for involvement of tau in progressive supranuclear palsy. European Study Group on Atypical Parkinsonism Consortium.
Effect of ApoE and tau on age of onset of progressive supranuclear palsy and multiple system atrophy.
Enteric GFAP expression and phosphorylation in Parkinson's disease.
Eye movement deficits in X-linked dystonia-parkinsonism are related to striatal degeneration.
Guadeloupean parkinsonism: a cluster of progressive supranuclear palsy-like tauopathy.
Lewy bodies in progressive supranuclear palsy represent an independent disease process.
Magnetic resonance imaging distinguishes progressive supranuclear palsy from multiple system atrophy.
Metabolic network expression in parkinsonism: Clinical and dopaminergic correlations.
MIBG myocardial scintigraphy in progressive supranuclear palsy.
Midbrain atrophy related to parkinsonism in a non-coding repeat expansion disorder: five cases of spinocerebellar ataxia type 31 with nigrostriatal dopaminergic dysfunction.
Morning glory sign: a particular MR finding in progressive supranuclear palsy.
MRI derived brain atrophy in PSP and MSA-P. Determining sample size to detect treatment effects.
Mutations in bassoon in individuals with familial and sporadic progressive supranuclear palsy-like syndrome.
Neurogenic bladder in progressive supranuclear palsy: A comparison with Parkinson's disease and multiple system atrophy.
Neuroimaging of PD, PSP, CBD and MSA-PET and SPECT studies.
Neuromelanin-sensitive magnetic resonance imaging in disease differentiation for parkinsonism or neurodegenerative disease affecting the basal ganglia.
Obsessive compulsive personality disorder in Progressive Supranuclear Palsy, Multiple System Atrophy and Essential Tremor.
Pathologic correlates of supranuclear gaze palsy with parkinsonism.
Patterns of brain atrophy in Parkinson's disease, progressive supranuclear palsy and multiple system atrophy.
Prevalence and Characteristics of Polyneuropathy in Atypical Parkinsonian Syndromes: An Explorative Study.
Prevalence of Submandibular Gland Synucleinopathy in Parkinson's Disease, Dementia with Lewy Bodies and other Lewy Body Disorders.
Progressive supranuclear palsy (PSP): Richardson syndrome and other PSP variants.
Progressive supranuclear palsy is not associated with neurogenic orthostatic hypotension.
Progressive supranuclear palsy presenting with urinary retention and sleep apnea.
Progressive Supranuclear Palsy with Predominant Cerebellar Ataxia.
Quantitative MRI measurement of superior cerebellar peduncle in progressive supranuclear palsy.
Speech disorders reflect differing pathophysiology in Parkinson's disease, progressive supranuclear palsy and multiple system atrophy.
The contribution of trigemino-cervical reflexes in distinguishing progressive supranuclear palsy from multiple system atrophy.
The unfolded protein response is activated in disease-affected brain regions in progressive supranuclear palsy and Alzheimer's disease.
Transcranial sonography in atypical parkinsonism: How reliable is it in real clinical practice? A multicentre comprehensive study.
Which ante mortem clinical features predict progressive supranuclear palsy pathology?
[A case of progressive supranuclear palsy associated with bilateral vocal cord abductor paralysis]
[An autopsy case of progressive supranuclear palsy with central pontine myelinolysis]
[PET and SPECT in Parkinson's disease]
[The application of Gallyas-Braak stainings in pathologic diagnosis of neurodegenerative diseases]
Muscle Cramp
Nocturnal manifestations of atypical and vascular parkinsonism: How do they differ from Parkinson's disease?
Muscle Rigidity
Progressive supranuclear palsy.
[Cerebral blood flow and oxygen metabolism in patients with pure akinesia and progressive supranuclear palsy]
Muscle Spasticity
Acoustical Analysis of Speech in Progressive Supranuclear Palsy.
Clinical speech impairment in Parkinson's disease, progressive supranuclear palsy, and multiple system atrophy.
Perceptual analysis of speech disorders in progressive supranuclear palsy.
Speech disorders reflect differing pathophysiology in Parkinson's disease, progressive supranuclear palsy and multiple system atrophy.
Myasthenia Gravis
[Clinical analysis of paralytic shellfish poisoning following ingestion of oysters]
Mycoses
Clinical application of presepsin as diagnostic biomarker of infection: overview and updates.
Toll recognition signal activates oenocytoid cell lysis via a crosstalk between plasmatocyte-spreading peptide and eicosanoids in response to a fungal infection.
Myeloproliferative Disorders
Gene dosage effect in acquired monosomy 7: distinct behaviour of beta-glucuronidase and phosphoserine phosphatase.
Myocardial Infarction
Presepsin (sCD14-ST): could it be a novel marker for the diagnosis of ST elevation myocardial infarction?
Myoclonus
Amantadine-induced myoclonus in a patient with progressive supranuclear palsy.
Progressive supranuclear palsy with palatal myoclonus.
[An autopsy case of progressive supranuclear palsy with olivary hypertrophy]
Myotonic Dystrophy
Coexistence of Progressive Supranuclear Palsy With Pontocerebellar Atrophy and Myotonic Dystrophy Type 1.
Tau-positive fine granules in the cerebral white matter: a novel finding among the tauopathies exclusive to parkinsonism-dementia complex of Guam.
Nasal Obstruction
Corrigendum.
Nasopharyngeal Carcinoma
A targeted nanocarrier based on polyspermine for the effective delivery of methotrexate in nasopharyngeal carcinoma.
Neonatal Sepsis
The Role of Pancreatic Stone Protein in Diagnosis of Early Onset Neonatal Sepsis.
Neoplasm Metastasis
Benign tumor behaves malignantly: a case report of bilateral multiple pulmonary sclerosing pneumocytoma.
Case Report: Rare Pulmonary Sclerosing Pneumocytoma: Large, Multiple, Metastatic, and Fatal.
Clinical and histopathologic features of pulmonary sclerosing pneumocytoma with dense spindle stromal cells and lymph node metastasis.
Fluoroscopy-Guided Percutaneous Sacroplasty for Painful Metastases at the Sacral Ala.
Large pulmonary sclerosing pneumocytoma with massive necrosis and vascular invasion: a case report.
Parenchyma-Sparing Resections for Pancreatic Neuroendocrine Tumors.
Percutaneous Sacroplasty for Painful Sacral Metastases Involving Multiple Sacral Vertebral Bodies: Initial Experience with an Interpedicular Approach.
Pulmonary sclerosing pneumocytoma with mediastinal lymph node metastasis: a case report.
Radiation necrosis presenting as pseudoprogression (PsP) during alectinib treatment of previously radiated brain metastases in ALK-positive NSCLC: Implications for disease assessment and management.
Single agent polysaccharopeptide delays metastases and improves survival in naturally occurring hemangiosarcoma.
Understanding symptomatic experience, impact, and emotional response in recently diagnosed metastatic castration-resistant prostate cancer: a qualitative study.
[Resection of gastric carcinoma with preserving of the spleen and pancreas and functional clearance lymph nodes of the spleen hillus and splenic artery]
Neoplasms
A 4-bp deletion in the Birt-Hogg-Dubé gene (FLCN) causes dominantly inherited spontaneous pneumothorax.
A case of pulmonary sclerosing pneumocytoma diagnosed preoperatively using transbronchial cryobiopsy.
A meta-analysis of the pros and cons of partial superficial parotidectomy versus superficial parotidectomy for the treatment of benign parotid neoplasms.
A murine preclinical syngeneic transplantation model for breast cancer precision medicine.
A photo-responsive peptide- and asparagine-glycine-arginine (NGR) peptide-mediated liposomal delivery system.
A Preliminary Study on Machine Learning-Based Evaluation of Static and Dynamic FET-PET for the Detection of Pseudoprogression in Patients with IDH-Wildtype Glioblastoma.
A Retrospective Case-Control Study on the Chest Wall and Lung Characteristics in Patients with Primary Spontaneous Pneumothorax.
A study on immunomodulatory mechanism of Polysaccharopeptide mediated by TLR4 signaling pathway.
Activation of peritoneal macrophages by polysaccharopeptide from the mushroom, Coriolus versicolor.
Activation of PP2A and Inhibition of mTOR Synergistically Reduce MYC Signaling and Decrease Tumor Growth in Pancreatic Ductal Adenocarcinoma.
Alterations of the PPP2R1B gene located at 11q23 in human colorectal cancers.
Analysis of pseudoprogression after proton or photon therapy of 99 patients with low grade and anaplastic glioma.
Analysis of the F-18 FDG PET/CT features of pulmonary sclerosing pneumocytoma.
Analyzing the capability of PSP, PCT and sCD25 to support the diagnosis of infection in cancer patients with febrile neutropenia.
Antioxidant, Antityrosinase and Antitumor Activity Comparison: The Potential Utilization of Fibrous Root Part of Bletilla striata (Thunb.) Reichb.f.
Autophagy regulates levels of tumor suppressor enzyme protein phosphatase 6.
Birt-Hogg-Dube Syndrome with a Novel Mutation in the FLCN Gene.
Can Tumor Location on Pre-treatment MRI Predict Likelihood of Pseudo-Progression vs. Tumor Recurrence in Glioblastoma?-A Feasibility Study.
Cancerous stem cells can arise from pediatric brain tumors.
Case Report: Rare Pulmonary Sclerosing Pneumocytoma: Large, Multiple, Metastatic, and Fatal.
Cell cycle-independent regulation of p21Waf1/Cip1 and retinoblastoma protein during okadaic acid-induced apoptosis is coupled with induction of Bax protein in human breast carcinoma cells.
Characterization and Immunological Activities of Polysaccharides from Polygonatum sibiricum.
Chemo- and radio-protective effects of polysaccharide of Spirulina platensis on hemopoietic system of mice and dogs.
Chemopreventive effect of PSP through targeting of prostate cancer stem cell-like population.
Clinical features in association with neurodegenerative diseases and malignancies.
Clinical Utility of Different Approaches for Detection of Late Pseudoprogression in Glioblastoma With O-(2-[18F]Fluoroethyl)-L-Tyrosine PET.
cMyc-mediated activation of serine biosynthesis pathway is critical for cancer progression under nutrient deprivation conditions.
Comparison of postoperative complications and facial nerve recovery rates after conventional and partial superficial parotidectomy of benign parotid tumours: a prospective study.
Comparison of prostate secretory protein with prostate specific antigen and prostatic acid phosphatase as a serum biomarker for diagnosis and monitoring patients with prostate carcinoma.
Coriolus versicolor polysaccharide peptide slows progression of advanced non-small cell lung cancer.
Coriolus versicolor polysaccharopeptide as an immunotherapeutic in China.
DC-AL GAN: Pseudoprogression and true tumor progression of glioblastoma multiform image classification based on DCGAN and AlexNet.
Diagnosis of pseudoprogression in patients with glioblastoma using O-(2-[(18)F]fluoroethyl)-L-tyrosine PET.
Differences in association of the serine/threonine protein phosphatase PP-2A with microtubules of metastatic and nonmetastatic tumor cells.
Distinguishing Pseudoprogression From True Early Progression in Isocitrate Dehydrogenase Wild-Type Glioblastoma by Interrogating Clinical, Radiological, and Molecular Features.
Dose-response and threshold analysis of tumor prevalence after intratracheal instillation of six types of low- and high-surface-area particles in a chronic rat experiment.
Down regulation of a novel protein, PSP, in rat hepatoma cdRLh 84-beared tumor.
Downregulation of CPI-17 contributes to dysfunctional motility in chronic intestinal inflammation model mice and ulcerative colitis patients.
Effects of polysaccharide peptide (PSP) from Coriolus versicolor on the pharmacokinetics of cyclophosphamide in the rat and cytotoxicity in HepG2 cells.
Efficacy of an anti-cancer strategy targeting SET in canine osteosarcoma.
Enhanced small interfering RNA delivery into cells by exploiting the additive effect between photo-sensitive peptides and targeting ligands.
Enzyme pathology and the histologic categorization of human lung tumors: the continuum of quantitative biochemical indices of neoplasticity.
Enzymic composition and growth rate of human pleural mesothelioma transplants in nude mice.
Estrogen regulation of phosphoserine phosphatase during regression and recrudescence of female reproductive organs.
Evaluation of polysaccharopeptide effects against C6 glioma in combination with radiation.
Fungal polysaccharopeptide inhibits tumor angiogenesis and tumor growth in mice.
Gene mutations in stool from gastric and colorectal neoplasia patients by next-generation sequencing.
Genome profile in a extremely rare case of pulmonary sclerosing pneumocytoma presenting with diffusely-scattered nodules in the right lung.
Glioblastoma radiomics: can genomic and molecular characteristics correlate with imaging response patterns?
Huge Pulmonary Sclerosing Pneumocytoma with Endobronchial Invasion: A Case Report with a Literature Review.
Human pancreatic cancer contains a side population expressing cancer stem cell-associated and prognostic genes.
Identification of biomarkers for pseudo and true progression of GBM based on radiogenomics study.
Immunomodulatory Properties of Coriolus versicolor: The Role of Polysaccharopeptide.
Immunoregulatory and Anti-Tumor Effects of Polysaccharopeptide and Astragalus polysaccharides on Tumor-Bearing Mice.
Immunostimulatory Effects of Polysaccharides from Spirulina platensis In Vivo and Vitro and Their Activation Mechanism on RAW246.7 Macrophages.
Immunotherapy with low-dose interleukin-2 and a polysaccharopeptide derived from Coriolus versicolor.
Inhaled particles and lung cancer, part B: paradigms and risk assessment.
Inhibition of phosphoserine phosphatase enhances the anticancer efficacy of 5-fluorouracil in colorectal cancer.
Inhibitory effects of polysaccharide extract from Spirulina platensis on corneal neovascularization.
Late Pseudoprogression in Glioblastoma: Diagnostic Value of Dynamic O-(2-[18F]fluoroethyl)-L-Tyrosine PET.
Machine learning-based investigation of the cancer protein secretory pathway.
Modulation of antipyrine clearance by polysaccharide peptide (PSP) isolated from Coriolus versicolor in the rat.
Molecular and histologic characteristics of pseudoprogression in diffuse gliomas.
Molecular characterization of Coriolus versicolor PSP-induced apoptosis in human promyelotic leukemic HL-60 cells using cDNA microarray.
Monitoring hydrogen polysulfide during ferroptosis with a two-photon fluorescent probe.
Parenchyma-Sparing Resections for Pancreatic Neuroendocrine Tumors.
Peptide-enhanced tumor accumulation of upconversion nanoparticles for sensitive upconversion luminescence/magnetic resonance dual-mode bioimaging of colorectal tumors.
Peptide-Induced Self-Assembly of Therapeutics into a Well-Defined Nanoshell with Tumor-Triggered Shape and Charge Switch.
Persistent socket pain postenucleation and post evisceration: a systematic review.
Phosphatase magnesium-dependent 1 ? (PPM1D), serine/threonine protein phosphatase and novel pharmacological target in cancer.
Phosphoserine Phosphatase Is a Novel Prognostic Biomarker on Chromosome 7 in Colorectal Cancer.
PI3K/Akt mediates expression of TNF-alpha mRNA and activation of NF-kappaB in calyculin A-treated primary osteoblasts.
Pleomorphic adenoma: extracapsular dissection versus partial superficial parotidectomy with facial nerve dissection.
Pleural granuloma mimicking malignancy 42 years after slurry talc injection for primary spontaneous pneumothorax.
Polygonatum sibiricum polysaccharides play anti-cancer effect through TLR4-MAPK/NF-?B signaling pathways.
Polysaccharide peptide (PSP) restores immunosuppression induced by cyclophosphamide in rats.
Polysaccharide peptide from Coriolus versicolor induces interleukin 6-related extension of endotoxin fever in rats.
Polysaccharide peptides from COV-1 strain of Coriolus versicolor induce hyperalgesia via inflammatory mediator release in the mouse.
Polysaccharopeptide enhanced the anti-cancer effect of gamma-tocotrienol through activation of AMPK.
Polysaccharopeptide enhances the anticancer activity of doxorubicin and etoposide on human breast cancer cells ZR-75-30.
Polysaccharopeptide exerts immunoregulatory effects via MyD88-dependent signaling pathway.
Polysaccharopeptides derived from Coriolus versicolor potentiate the S-phase specific cytotoxicity of Camptothecin (CPT) on human leukemia HL-60 cells.
Positive Resection Margins Detected by Standardized Study of a Pancreaticoduodenectomy Sample: Is There Any Real Impact on Long-term Survival?
Potential impact of the Affordable Care Act's preventive services provision on breast cancer stage: A preliminary assessment.
Potential of a novel polysaccharide preparation (GLPP) from Anhui-grown Ganoderma lucidum in tumor treatment and immunostimulation.
Preclinical and clinical studies of Coriolus versicolor polysaccharopeptide as an immunotherapeutic in China.
Primary spontaneous pneumothorax in children: factors predicting recurrence and contralateral occurrence.
Prognostic value of flow cytometry in surgically treated primary gastric lymphoma.
Protein phosphatase 2A regulatory subunits and cancer.
PSP activates monocytes in resting human peripheral blood mononuclear cells: Immunomodulatory implications for cancer treatment.
PSPH induces cell autophagy and promotes cell proliferation and invasion in the hepatocellular carcinoma cell line Huh7 via the AMPK/mTOR/ULK1 signaling pathway.
PSPH Mediates the Metastasis and Proliferation of Non-small Cell Lung Cancer through MAPK Signaling Pathways.
Pulmonary sclerosing pneumocytoma demonstrating intratumoral hematoma.
Pulmonary sclerosing pneumocytoma in an 18-year-old male patient: A case report and literature review.
Recent Advances and Challenges in Studies of Control of Cancer Stem Cells and the Gut Microbiome by the Trametes-Derived Polysaccharopeptide PSP (Review).
Relationships of parathyroid hormone, parathyroid secretory protein, parathyroid hormone messenger RNA, parathyroid secretory protein mRNA, and replication in human parathyroid adenoma and secondary hyperplasia tissues and cultures.
Relevance of the rat lung tumor response to particle overload for human risk assessment-Update and interpretation of new data since ILSI 2000.
Review of surgical techniques and guide for decision making in the treatment of benign parotid tumors.
Single agent polysaccharopeptide delays metastases and improves survival in naturally occurring hemangiosarcoma.
Surgical interventions for management of benign parotid tumors: A systematic review and network meta-analysis.
Systemic siRNA delivery to tumors by cell-penetrating ?-helical polypeptide-based metastable nanoparticles.
Targeting inhibitor 2 of protein phosphatase 2A as a therapeutic strategy for prostate cancer treatment.
The cell death process of the anticancer agent polysaccharide-peptide (PSP) in human promyelocytic leukemic HL-60 cells.
The predictive value of absolute lymphocyte counts on tumor progression and pseudoprogression in patients with glioblastoma.
The proximal serrated polyp detection rate is an easy-to-measure proxy for the detection rate of clinically relevant serrated polyps.
The significance of the margin in parotid surgery for pleomorphic adenoma.
The use of mushroom glucans and proteoglycans in cancer treatment.
The value of MGMT promote methylation and IDH-1 mutation on diagnosis of pseudoprogression in patients with high-grade glioma: A meta-analysis.
Thrombotic thrombocytopenic purpura associated with clopidogrel: further evaluation.
Toxicokinetics and effects of fibrous and nonfibrous particles.
Trametes versicolor (Synn. Coriolus versicolor) Polysaccharides in Cancer Therapy: Targets and Efficacy.
Update of the Swedish Two-County Trial of breast cancer screening: histologic grade-specific and age-specific results.
Upregulation of phosphoserine phosphatase contributes to tumor progression and predicts poor prognosis in non-small cell lung cancer patients.
[Analysis of Clinical Characteristics of 35 Cases ?of Pulmonary Sclerosing Pneumocytoma].
[Effect of polysaccharide from Spirulina platensis on hematopoietic cells proliferation, apoptosis and Bcl-2 expression in mice bearing tumor treated with chemotherapy]
[Immunomodulatory and antitumor properties of polysaccharide peptide (PSP)].
[Immunoregulatory activity of polysaccharopeptide and astragalus polysaccharides on EAC tumor-bearing mice]
[Minisatellite instability induced by okadaic acid]
[Partial superficial parotidectomy versus superficial parotidectomy for treatment of parotid benign tumors: evidence-based medicine analysis].
[Retrospective study of partial superficial parotidectomy and superficial parotidectomy on superficial parotid benign tumor].
Nephritis
[Clinico-biochemical study of experimental renal injuries in rats. 3. Relations between serum half-life of phenolsulfonphthalein and renal injuries]
Nervous System Diseases
A comparison of tau protein in cerebrospinal fluid between corticobasal degeneration and progressive supranuclear palsy.
A Histologic Study of the Circadian System in Parkinson Disease, Multiple System Atrophy, and Progressive Supranuclear Palsy.
Accuracy of clinical diagnosis of progressive supranuclear palsy.
Accuracy of the National Institute for Neurological Disorders and Stroke/Society for Progressive Supranuclear Palsy and Neuroprotection and Natural History in Parkinson Plus Syndromes Criteria for the Diagnosis of Progressive Supranuclear Palsy.
Are the International Parkinson disease and Movement Disorder Society progressive supranuclear palsy (IPMDS-PSP) diagnostic criteria accurate enough to differentiate common PSP phenotypes?
Atrophy in midbrain & cerebral/cerebellar pedunculi is characteristic for progressive supranuclear palsy - A double-validation whole-brain meta-analysis.
Characterizing swallowing abnormalities in progressive supranuclear palsy.
Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria.
Clinical features and natural history of progressive supranuclear palsy: a clinical cohort study.
Clinical heterogeneity in progressive supranuclear palsy: Problems of clinical diagnostic criteria of NINDS-SPSP in a retrospective study of seven Japanese autopsy cases.
Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): report of the NINDS-SPSP international workshop.
Correlation between qualitative balance indices, dynamic posturography and structural brain imaging in patients with progressive supranuclear palsy and its subtypes.
Diagnostic accuracy of Magnetic Resonance Parkinsonism Index in differentiating progressive supranuclear palsy from Parkinson's disease and controls in Indian patients.
Diagnostic validity of magnetic resonance parkinsonism index in differentiating patients with progressive supranuclear palsy from patients with Parkinson's disease.
Familial aggregation of parkinsonism in progressive supranuclear palsy.
Freezing of gait is an early clinical feature of progressive supranuclear palsy.
Lack of association between progressive supranuclear palsy and arterial hypertension: a clinicopathological study.
Neurodegenerative disorders mimicking progressive supranuclear palsy: a report of three cases.
Phenotypic Variants of Patients with Progressive Supranuclear Palsy.
Preliminary NINDS neuropathologic criteria for Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy).
Progression of dysarthria and dysphagia in postmortem-confirmed parkinsonian disorders.
Progression of falls in postmortem-confirmed parkinsonian disorders.
Progression of gait, speech and swallowing deficits in progressive supranuclear palsy.
Progressive supranuclear palsy combined with Alzheimer's disease: A clinicopathological study of two autopsy cases.
Progressive supranuclear palsy in a sample of Brazilian population: clinical features of 16 patients.
Progressive supranuclear palsy with wall-eyed bilateral internuclear ophthalmoplegia syndrome.
Progressive supranuclear palsy.
Rate of decline in progressive supranuclear palsy.
Smad ubiquitination regulatory factor-2 in progressive supranuclear palsy.
Specificity and sensitivity of magnetic resonance imaging findings in the diagnosis of progressive supranuclear palsy.
The prevalence of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) in the UK.
Understanding the relationship between freezing of gait and other progressive supranuclear palsy features.
Neurobehavioral Manifestations
Alterations of GABAergic neurons in the basal ganglia of patients with progressive supranuclear palsy: an in situ hybridization study of GAD67 messenger RNA.
Burden on caregivers of schizophrenia outpatients in Brazil: Relationship to symptomatology and functioning.
Cerebral hypometabolism in progressive supranuclear palsy studied with positron emission tomography.
Cognitive-behavioural features of progressive supranuclear palsy syndrome overlap with frontotemporal dementia.
Predictors of survival in progressive supranuclear palsy and multiple system atrophy: a systematic review and meta-analysis.
Zolpidem in progressive supranuclear palsy.
Neuroblastoma
An improved sensitive assay for the detection of PSP toxins with neuroblastoma cell-based impedance biosensor.
Application of the neuroblastoma assay for paralytic shellfish poisons to neurotoxic freshwater cyanobacteria: interlaboratory calibration and comparison with other methods of analysis.
Characterization of human and rat immortalized clones parotid acinar cells with respect to specific proteins and their mRNAs, and receptor-linked adenylate cyclase.
Differential effects of physostigmine and organophosphates on nicotinic receptors in neuronal cells of different species.
Effects of organophosphorus compounds on ATP production and mitochondrial integrity in cultured cells.
Protective effect of polysaccharide peptide on cerebral ischemia?reperfusion injury in rats.
Neurodegenerative Diseases
A?1-15/16 as a potential diagnostic marker in neurodegenerative diseases.
Advances in progressive supranuclear palsy: new diagnostic criteria, biomarkers, and therapeutic approaches.
Alpha-synuclein Levels in the Differential Diagnosis of Lewy Bodies Dementia and Other Neurodegenerative Disorders: A Meta-analysis.
An extended 5'-tau susceptibility haplotype in progressive supranuclear palsy.
Apraxia of speech and nonfluent aphasia: a new clinical marker for corticobasal degeneration and progressive supranuclear palsy.
Association of MAPT Subhaplotypes With Risk of Progressive Supranuclear Palsy and Severity of Tau Pathology.
Astrocytes expressing hyperphosphorylated tau protein without glial fibrillary tangles in argyrophilic grain disease.
Atrophy of superior cerebellar peduncle in progressive supranuclear palsy.
Brain aconitase activity is not decreased in progressive supranuclear palsy.
Cerebral oxygen metabolism in patients with progressive supranuclear palsy: a positron emission tomography study.
Characteristics of progressive supranuclear palsy presenting with corticobasal syndrome: a cortical variant.
Clinical features in association with neurodegenerative diseases and malignancies.
Clusterin CSF levels in differential diagnosis of neurodegenerative disorders.
Comprehensive mRNA expression profiling distinguishes tauopathies and identifies shared molecular pathways.
Current and future treatments in progressive supranuclear palsy.
Development of a grape seed polyphenolic extract with anti-oligomeric activity as a novel treatment in progressive supranuclear palsy and other tauopathies.
Factors associated with development and distribution of granular/fuzzy astrocytes in neurodegenerative diseases.
Familial progressive supranuclear palsy. Description of a pedigree and review of the literature.
Freezing of gait is an early clinical feature of progressive supranuclear palsy.
Frontrunner in Translation: Progressive Supranuclear Palsy.
High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy.
In vivo binding of a tau imaging probe, [11 C]PBB3, in patients with progressive supranuclear palsy.
Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases.
Lack of association between progressive supranuclear palsy and arterial hypertension: a clinicopathological study.
Long lasting pure freezing of gait preceding progressive supranuclear palsy: A clinicopathological study.
Magnetic resonance imaging in progressive supranuclear palsy.
Medical decision-making in progressive supranuclear palsy: A comparison to other neurodegenerative disorders.
Molecular Processing of Tau Protein in Progressive Supranuclear Palsy: Neuronal and Glial Degeneration.
Mutations in bassoon in individuals with familial and sporadic progressive supranuclear palsy-like syndrome.
Myocardial (123)I-MIBG scintigraphy in patients with PSP, CBD and MSA.
Neuromelanin-sensitive magnetic resonance imaging in disease differentiation for parkinsonism or neurodegenerative disease affecting the basal ganglia.
Neuropathologic differentiation of progressive supranuclear palsy and corticobasal degeneration.
Olfaction in Neuropathologically Defined Progressive Supranuclear Palsy.
Pattern of Tau forms in CSF is altered in progressive supranuclear palsy.
Polymorphisms in the tau gene in sporadic frontotemporal dementia and other neurodegenerative disorders.
Prediagnostic motor and non-motor symptoms in progressive supranuclear palsy: The step-back PSP study.
Progressive Supranuclear Palsy - A Case Study from the Perspective of a Primary Care Physician Son.
Progressive supranuclear palsy often develops idiopathic normal pressure hydrocephalus-like magnetic resonance imaging features.
Progressive Supranuclear Palsy with Wall-Eyed Bilateral Internuclear Ophthalmoplegia Syndrome: Authors' Second Case.
Progressive supranuclear palsy.
Progressive Supranuclear Palsy: A Current Review.
Progressive supranuclear palsy: a review of co-existing neurodegeneration.
Progressive Supranuclear Palsy: Improvement in Cognitive-Behavioral Disturbances and Motor-Function Disabilities Following Treatment With Antidepressants and Cholinesterase Inhibitors.
Progressive supranuclear palsy: neuropathologic and clinical heterogeneity.
Psychometric properties of the Beck Depression Inventory-II in progressive supranuclear palsy.
Stimulation over the cerebellum with a regular figure-of-eight coil induces reduced motor cortex inhibition in patients with progressive supranuclear palsy.
Structural basis of dementia in neurodegenerative disorders.
STX6 rs1411478 is not associated with increased risk of Parkinson's disease.
Susceptibility MRI captures nigral pathology in patients with parkinsonian syndromes.
Tau imaging with [(18) F]THK-5351 in progressive supranuclear palsy.
Tau Pathology Drives Dementia Risk-Associated Gene Networks toward Chronic Inflammatory States and Immunosuppression.
The Progressive Supranuclear Palsy: Past and Present Aspects.
The tau gene A0 allele and progressive supranuclear palsy.
To be or not to be: PP2A as a dual player in CNS functions, its role in neurodegeneration, and its interaction with brain insulin signaling.
Transglutaminase-induced cross-linking of tau proteins in progressive supranuclear palsy.
[11C]PK11195 binding in Alzheimer disease and progressive supranuclear palsy.
[A case of progressive supranuclear palsy associated with bilateral vocal cord abductor paralysis]
[Advance of SPECT: differential diagnosis and evaluation of pathophysiology of neurodegenerative disorders]
[MRI diagnosis of neurodegenerative disorders]
[Progressive supranuclear palsy].
[The application of Gallyas-Braak stainings in pathologic diagnosis of neurodegenerative diseases]
[Treatment of progressive supranuclear palsy]
Neuroendocrine Tumors
Parenchyma-Sparing Resections for Pancreatic Neuroendocrine Tumors.
Neuroinflammatory Diseases
Age-dependent neuroinflammation and cognitive decline in a novel Ala152Thr-Tau transgenic mouse model of PSP and AD.
Cytokine expression and microglial activation in progressive supranuclear palsy.
Microglial Activation and Inflammation as a Factor in the Pathogenesis of Progressive Supranuclear Palsy (PSP).
Neuroinflammation and tau co-localize in vivo in progressive supranuclear palsy.
Neuroinflammation predicts disease progression in progressive supranuclear palsy.
Neutrophil-to-lymphocyte ratio (NLR) at boundaries of Progressive Supranuclear Palsy Syndrome (PSPS) and Corticobasal Syndrome (CBS).
[11C]PK11195 binding in Alzheimer disease and progressive supranuclear palsy.
Neurologic Manifestations
On the phenotypic spectrum of serine biosynthesis defects.
Neuroma
Persistent socket pain postenucleation and post evisceration: a systematic review.
Nutrition Disorders
Radiolucent and calcified pancreatic lithiasis: two different diseases. Role of alcohol and heredity.
Obesity
Psycho-Physiological Responses to a 4-Month High-Intensity Interval Training-Centered Multidisciplinary Weight-Loss Intervention in Adolescents with Obesity.
Purple Sweet Potato Attenuate Weight Gain in High Fat Diet Induced Obese Mice.
Olfaction Disorders
A Card-type Odor Identification Test for Japanese Patients with Parkinson's Disease and Related Disorders.
Oligodendroglioma
Analysis of pseudoprogression after proton or photon therapy of 99 patients with low grade and anaplastic glioma.
Codeletions at 1p and 19q predict a lower risk of pseudoprogression in oligodendrogliomas and mixed oligoastrocytomas.
Olivopontocerebellar Atrophies
Magnetic resonance imaging distinguishes progressive supranuclear palsy from multiple system atrophy.
[Vertical oculomotor disorders in progressive supranuclear palsy and spino-cerebellar degeneration]
Ophthalmoplegia
Clinical, MRI and 18F-FDG-PET/CT analysis of progressive supranuclear palsy.
Critical appraisal of the role of davunetide in the treatment of progressive supranuclear palsy.
Current and future treatments in progressive supranuclear palsy.
Exodeviated ophthalmoplegia in a patient with progressive supranuclear palsy.
Eyelid motor abnormalities in progressive supranuclear palsy.
Increased tau burden in the cortices of progressive supranuclear palsy presenting with corticobasal syndrome.
Long-term follow-up of deep brain stimulation of peduncolopontine nucleus in progressive supranuclear palsy: Report of three cases.
Neuro-ophthalmic findings in progressive supranuclear palsy.
Progressive supranuclear palsy and corticobasal ganglionic degeneration: differentiation by clinical features and neuroimaging techniques.
Progressive supranuclear palsy diagnosis and confounding features: report on 16 autopsied cases.
Progressive supranuclear palsy.
Progressive supranuclear palsy. Clinical and pharmacologic update.
[Cerebral blood flow and oxygen metabolism in patients with pure akinesia and progressive supranuclear palsy]
[Improvement of ophthalmoplegia by 5-hydroxytryptophan in two cases of progressive supranuclear palsy]
[Progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): report of a case and review of the literature]
[Progressive supranuclear palsy]
[Widespread argentophilic structures in progressive supranuclear palsy--an autopsy case report]
Osteoarthritis
Effect of non-steroidal anti-inflammatory drugs on osteoarthritis of the knee. With special reference to PSP clearance as an indicator.
Effect of Non-Steroidal Anti-Inflammatory Drugs on Osteoarthritis of the Knee: With Special Reference to PSP Clearance as an Indicator.
[Articular PSP clearance in osteoarthritis of the knee]
[Effect of non-steroid anti-inflammatory drugs for osteoarthritis of the knee; PSP clearance test]
Osteoarthritis, Knee
Effect of non-steroidal anti-inflammatory drugs on osteoarthritis of the knee. With special reference to PSP clearance as an indicator.
Effect of Non-Steroidal Anti-Inflammatory Drugs on Osteoarthritis of the Knee: With Special Reference to PSP Clearance as an Indicator.
[Articular PSP clearance in osteoarthritis of the knee]
[Effect of non-steroid anti-inflammatory drugs for osteoarthritis of the knee; PSP clearance test]
Osteolysis
Polygonatum sibiricum polysaccharide inhibits osteoporosis by promoting osteoblast formation and blocking osteoclastogenesis through Wnt/?-catenin signalling pathway.
Osteomyelitis
Procalcitonin and Pancreatic Stone Protein Function as Biomarkers in Early Diagnosis of Pediatric Acute Osteomyelitis.
Osteoporosis
Abnormal bone mineral density and bone turnover marker expression profiles in patients with primary spontaneous pneumothorax.
Effects of Polygonatum sibiricum polysaccharide on the osteogenic differentiation of bone mesenchymal stem cells in mice.
Polygonatum sibiricum polysaccharide inhibits osteoporosis by promoting osteoblast formation and blocking osteoclastogenesis through Wnt/?-catenin signalling pathway.
Polygonatum Sibiricum Polysaccharide Promotes Osteoblastic Differentiation Through the ERK/GSK-3?/?-Catenin Signaling Pathway In Vitro.
The Role and Mechanism of miRNA-1224 in the Polygonatum Sibiricum Polysaccharide Regulation of Bone Marrow-Derived Macrophages to Osteoclast Differentiation.
Ovarian Neoplasms
Independent action of serine/threonine protein phosphatase in ovarian cancer plasma membrane and cytosol during gonadotropin-releasing hormone stimulation.
Pancreatic Diseases
Current status of pancreatic stone protein.
Pancreatic Fistula
Parenchyma-Sparing Resections for Pancreatic Neuroendocrine Tumors.
Pancreatic Neoplasms
Serum pancreatic stone protein in pancreatic diseases.
Pancreaticobiliary Maljunction
Activated pancreatic enzyme and pancreatic stone protein (PSP/reg) in bile of patients with pancreaticobiliary maljunction/ choledochal cysts.
Pancreatitis
Change of pancreatic enzymes, pancreatic stone protein (PSP), and plasma alpha(2)-macroglobulin-trypsin complex-like substance (MTLS) in the activation of pancreatic juice.
Chronic calcifying pancreatitis: epidemiology and current concept of the lithogenesis.
Exocrine meets endocrine: pancreatic stone protein and regenerating protein--two sides of the same coin.
Pancreatic Stent or Rectal Indomethacin-Which Better Prevents Post-ERCP Pancreatitis?: A Propensity Score Matching Analysis.
Pancreatic stone protein: quantification in pancreatic juice by enzyme-linked immunosorbent assay and comparison with other methods.
Prophylactic effect of rectal indomethacin plus nitroglycerin administration for preventing pancreatitis after endoscopic retrograde cholangiopancreatography in female patients.
Role of Pancreatic Stone Protein as an Early Biomarker for Risk Stratification of Acute Pancreatitis.
Serum pancreatic stone protein in pancreatic diseases.
Trans-heterozygosity for mutations enhances the risk of recurrent/chronic pancreatitis in patients with Cystic Fibrosis.
[Analysis of pancreatic stone protein gene of hereditary pancreatitis]
Pancreatitis, Chronic
Current status of pancreatic stone protein.
Idiopathic chronic calcifying pancreatitis with diabetes mellitus. Analysis of pancreatic stone protein gene.
Immunocytochemical localization of pancreatic stone protein in the human digestive tract.
Organic matrix of pancreatic stones associated with nutritional pancreatitis.
Pancreatic stone protein and lactoferrin in human pancreatic juice in chronic pancreatitis.
Serum pancreatic stone protein in pancreatic diseases.
[Clinical trial on pancreatic duct stones caused by chronic pancreatitis.]
Panniculitis
Poststeroid panniculitis.
Paralysis
A new noninvasive test to detect mitochondrial dysfunction of skeletal muscles in progressive supranuclear palsy.
Accuracy of clinical criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome).
Accuracy of clinical diagnosis of progressive supranuclear palsy.
Accuracy of the National Institute for Neurological Disorders and Stroke/Society for Progressive Supranuclear Palsy and Neuroprotection and Natural History in Parkinson Plus Syndromes Criteria for the Diagnosis of Progressive Supranuclear Palsy.
Alterations of 3,4-dihydroxyphenylethylamine and its metabolite 3,4-dihydroxyphenylacetic produced in rat brain tissues after systemic administration of saxitoxin.
An autopsy-confirmed case of progressive supranuclear palsy with predominant postural instability.
An Evaluation of the Progressive Supranuclear Palsy Speech/Language Variant.
An extended 5'-tau susceptibility haplotype in progressive supranuclear palsy.
Anti-tau phospho-specific Ser262 antibody recognizes a variety of abnormal hyper-phosphorylated tau deposits in tauopathies including Pick bodies and argyrophilic grains.
APOE E4 is a determinant for Alzheimer type pathology in progressive supranuclear palsy.
Are the International Parkinson disease and Movement Disorder Society progressive supranuclear palsy (IPMDS-PSP) diagnostic criteria accurate enough to differentiate common PSP phenotypes?
Assessment of midbrain atrophy in patients with progressive supranuclear palsy with routine magnetic resonance imaging.
Association of an extended haplotype in the tau gene with progressive supranuclear palsy.
Association of Tripartite Motif Containing 11 rs564309 with Tau Pathology in Progressive Supranuclear Palsy.
Automated Brainstem Segmentation Detects Differential Involvement in Atypical Parkinsonian Syndromes.
Balance and eye movement training to improve gait in people with progressive supranuclear palsy: quasi-randomized clinical trial.
Behavioral changes as the earliest clinical manifestation of progressive supranuclear palsy.
Blood-based NfL: A biomarker for differential diagnosis of parkinsonian disorder.
Blood-Brain Barrier Dysfunction as a Hallmark Pathology in Chronic Traumatic Encephalopathy.
Can the frontal assessment battery (FAB) differentiate bradykinetic rigid syndromes? Relation of the FAB to formal neuropsychological testing.
Caregiving in progressive supranuclear palsy.
Cerebral blood flow in corticobasal degeneration and progressive supranuclear palsy.
Cerebral oxygen metabolism in patients with progressive supranuclear palsy: a positron emission tomography study.
Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism.
Cholinergic cortical circuits in Parkinson's disease and in progressive supranuclear palsy: a transcranial magnetic stimulation study.
Clinical correlates of longitudinal brain atrophy in progressive supranuclear palsy.
Clinical features and natural history of progressive supranuclear palsy: a clinical cohort study.
Clinical features differentiating patients with postmortem confirmed progressive supranuclear palsy and corticobasal degeneration.
Clinical features of dystonia in atypical parkinsonism.
Clinical Features of Patients with Concomitant Parkinson's Disease and Progressive Supranuclear Palsy Pathology.
Clinical genetics of familial progressive supranuclear palsy.
Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): report of the NINDS-SPSP international workshop.
Cognitive decline on the Repeatable Battery for the Assessment of Neuropsychological Status in progressive supranuclear palsy.
Cognitive disturbances in progressive supranuclear palsy.
Combination of dopamine transporter and D2 receptor SPECT in the diagnostic evaluation of PD, MSA, and PSP.
Comparison of clinical features in pathologically confirmed PSP and MSA patients followed at a tertiary center.
Comparison of motor, cognitive, and behavioral features in progressive supranuclear palsy and Parkinson's disease.
Comparison of natural histories of progressive supranuclear palsy and multiple system atrophy.
Conventional magnetic resonance imaging in confirmed progressive supranuclear palsy and multiple system atrophy.
Cortical Alzheimer Type Pathology Does Not Influence tau Pathology in Progressive Supranuclear Palsy.
Cortical atrophy differentiates Richardson's syndrome from the parkinsonian form of progressive supranuclear palsy.
Corticobasal degeneration with TDP-43 pathology presenting with progressive supranuclear palsy syndrome: a distinct clinicopathologic subtype.
CSF sAPP? and sAPP? levels in Alzheimer's Disease and Multiple Other Neurodegenerative Diseases: A Network Meta-Analysis.
Davunetide in patients with progressive supranuclear palsy: a randomised, double-blind, placebo-controlled phase 2/3 trial.
Deficits in long-term retention of learned motor skills in patients with cortical or subcortical degeneration.
Development and Validation of the Automated Imaging Differentiation in Parkinsonism (AID-P): A Multi-Site Machine Learning Study.
Diagnosis and management of progressive supranuclear palsy.
Difficulties in the diagnosis of four repeats (4R) tauopathic parkinsonian syndromes.
Distribution of tuft-shaped astrocytes in the cerebral cortex in progressive supranuclear palsy.
Early progressive supranuclear palsy: pathology and clinical presentation.
Effect of MAPT and APOE on prognosis of progressive supranuclear palsy.
Electrophysiological features of lower motor neuron involvement in progressive supranuclear palsy.
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases.
Executive dysfunction is the primary cognitive impairment in progressive supranuclear palsy.
Eye movements and association with regional brain atrophy in clinical subtypes of progressive supranuclear palsy.
Eye movements in parkinsonian syndromes.
Eyelid motor abnormalities in progressive supranuclear palsy.
Factors associated with development and distribution of granular/fuzzy astrocytes in neurodegenerative diseases.
Familial progressive supranuclear palsy: detection of subclinical cases using 18F-dopa and 18fluorodeoxyglucose positron emission tomography.
Frontal presentation in progressive supranuclear palsy.
FTLD-TDP and progressive supranuclear palsy in comorbidity-a report of two cases with different clinical presentations.
Functional correlates of vertical gaze palsy and other ocular motor deficits in PSP: an FDG-PET study.
Further extension of the H1 haplotype associated with progressive supranuclear palsy.
Gait Analysis in Progressive Supranuclear Palsy Phenotypes.
Gait analysis in PSP and NPH: Dual-task conditions make the difference.
Guadeloupean parkinsonism: a cluster of progressive supranuclear palsy-like tauopathy.
Health-related quality of life in patients with progressive supranuclear palsy.
Human positron emission tomographic [18F]fluorodopa studies correlate with dopamine cell counts and levels.
Imaging counterpart of postural instability and vertical ocular dysfunction in patients with PSP: A multimodal MRI study.
Impairment of eyeblink classical conditioning in progressive supranuclear palsy.
Improvement of gaze control after balance and eye movement training in patients with progressive supranuclear palsy: a quasi-randomized controlled trial.
Inferior olivary hypertrophy is uncommon in progressive supranuclear palsy.
Influence of target size on vertical gaze palsy in a pathologically proven case of progressive supranuclear palsy.
Lack of trigemino-cervical reflexes in progressive supranuclear palsy.
Late-onset frontotemporal dementia associated with progressive supranuclear palsy/argyrophilic grain disease/Alzheimer's disease pathology.
Levodopa-induced facial dystonia in a case of progressive supranuclear palsy.
Lifetime exposure to estrogen and progressive supranuclear palsy: Environmental and Genetic PSP study.
Magnetic resonance imaging distinguishes progressive supranuclear palsy from multiple system atrophy.
Measuring quality of life in PSP: the PSP-QoL.
Metabolic network expression in parkinsonism: Clinical and dopaminergic correlations.
Microtubule-associated protein tau genetic variations are uncommon cause of frontotemporal dementia in south India.
Midbrain atrophy is not a biomarker of progressive supranuclear palsy pathology.
Midbrain MRI assessments in progressive supranuclear palsy subtypes.
MM2 subtype of sporadic Creutzfeldt-Jakob disease may underlie the clinical presentation of progressive supranuclear palsy.
MR imaging of the superior profile of the midbrain: differential diagnosis between progressive supranuclear palsy and Parkinson disease.
MRI gray and white matter measures in progressive supranuclear palsy and corticobasal syndrome.
Natural clinical course of progressive supranuclear palsy in Chinese patients in Hong Kong.
Natural history of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) and clinical predictors of survival: a clinicopathological study.
Neuro-ophthalmic findings in progressive supranuclear palsy.
Neurofibrillary tangles in progressive supranuclear palsy contain the same tau epitopes identified in Alzheimer's disease PHFtau.
Neuroimaging of PD, PSP, CBD and MSA-PET and SPECT studies.
Neuropathologic basis of frontotemporal dementia in progressive supranuclear palsy.
New and reliable MRI diagnosis for progressive supranuclear palsy.
Obsessive compulsive personality disorder in Progressive Supranuclear Palsy, Multiple System Atrophy and Essential Tremor.
Parkinson disease and progressive supranuclear palsy: protein expression in skin.
Parkinsonian syndromes associated with hydrocephalus: case reports, a review of the literature, and pathophysiological hypotheses.
Parkinsonism with newly diagnosed flare-up rheumatoid arthritis mimicking progressive supranuclear palsy.
Patterns of brain atrophy in Parkinson's disease, progressive supranuclear palsy and multiple system atrophy.
Pontine-to-midbrain ratio indexes ocular-motor function and illness stage in adult Niemann-Pick disease type C.
Population based mortality and quality of death certification in progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome).
Possible relation of atypical parkinsonism in the French West Indies with consumption of tropical plants: a case-control study. Caribbean Parkinsonism Study Group.
Potential multisystem degeneration in Asidan patients.
Prediagnostic motor and non-motor symptoms in progressive supranuclear palsy: The step-back PSP study.
Predicting alpha-synuclein pathology by REM sleep behavior disorder diagnosis.
Prevalence and Characteristics of Polyneuropathy in Atypical Parkinsonian Syndromes: An Explorative Study.
Progression of gait, speech and swallowing deficits in progressive supranuclear palsy.
Progression of white matter damage in progressive supranuclear palsy with predominant parkinsonism.
Progressive nonfluent aphasia and subsequent aphasic dementia associated with atypical progressive supranuclear palsy pathology.
Progressive Supranuclear Gaze Palsy with Predominant Cerebellar Ataxia: A Case Series with Videos.
Progressive supranuclear palsy (PSP): Richardson syndrome and other PSP variants.
Progressive supranuclear palsy and corticobasal degeneration: lumping versus splitting.
Progressive supranuclear palsy responding to intravenous thiamine: superimposed Wernicke's encephalopathy?
Progressive supranuclear palsy syndrome presenting as progressive nonfluent aphasia: a neuropsychological and neuroimaging analysis.
Progressive supranuclear palsy with dementia: cortical pathology.
Progressive supranuclear palsy with wall-eyed bilateral internuclear ophthalmoplegia syndrome.
Progressive supranuclear palsy.
Progressive supranuclear palsy: a clinicopathological study of 21 cases.
Progressive Supranuclear Palsy: A Current Review.
Progressive supranuclear palsy: a survey of the disease course.
Progressive supranuclear palsy: neuropathologic and clinical heterogeneity.
Progressive supranuclear palsy: new disease or variant of postencephalitic parkinsonism?
Progressive Supranuclear Palsy: What do we know About it?
Quantitative evaluation of oculomotor disturbances in progressive supranuclear palsy.
Quantitative MRI measurement of superior cerebellar peduncle in progressive supranuclear palsy.
Quantitative proteomics identifies surfactant-resistant alpha-synuclein in cerebral cortex of parkinsonism-dementia complex of Guam but not alzheimer's disease or progressive supranuclear palsy.
Rate of decline in progressive supranuclear palsy.
Research goals in progressive supranuclear palsy. First International Brainstorming Conference on PSP.
Retinal degeneration in progressive supranuclear palsy measured by optical coherence tomography and scanning laser polarimetry.
Reversible progressive supranuclear palsy-like phenotype as an initial manifestation of HIV infection.
Salivary alpha-synuclein in the diagnosis of Parkinson's disease and Progressive Supranuclear Palsy.
Selective decrease of large neurons in the neostriatum in progressive supranuclear palsy.
Sensitivity and Specificity of Diagnostic Criteria for Progressive Supranuclear Palsy.
Side effects induced by the acute levodopa challenge in Parkinson's Disease and atypical parkinsonisms.
Sleep disturbances in the speech-language variant of progressive supranuclear palsy.
Spatial attention and spatial short term memory in PSP and Parkinson's disease.
Speech disorders reflect differing pathophysiology in Parkinson's disease, progressive supranuclear palsy and multiple system atrophy.
Spinocerebellar degeneration: Discrepancies between clinical and pathological diagnoses.
Structural and functional meta-analytic evidence for fronto-subcortical system deficit in progressive supranuclear palsy.
Subcortical damage and cortical dysfunction in progressive supranuclear palsy demonstrated by positron emission tomography.
Superficial or partial superficial parotidectomy for the treatment of primary benign parotid tumors.
Supranuclear gaze palsy and eyelid apraxia in postencephalitic parkinsonism.
The auditory startle response in parkinsonism may reveal the extent but not type of pathology.
The Cure PSP Care Guide: A Telephonic Nursing Intervention for Individuals and Families Living With Progressive Supranuclear Palsy.
The Dementia Rating Scale in Alzheimer's disease, Huntington's disease and progressive supranuclear palsy.
The diagnosis of neurodegenerative disorders based on clinical and pathological findings using an MRI approach.
The diagnosis of progressive supranuclear palsy: current opinions and challenges.
The Differential Diagnosis and Treatment of Atypical Parkinsonism.
The H1c haplotype at the MAPT locus is associated with Alzheimer's disease.
The Progressive Supranuclear Palsy: Past and Present Aspects.
The ratio of square wave jerk rates to blink rates distinguishes progressive supranuclear palsy from Parkinson disease.
The Role of Frontal Assessment Battery and Frontal Lobe Single-Photon Emission Computed Tomography in the Differential Diagnosis of Progressive Supranuclear Palsy Variants and Corticobasal Syndrome-A Pilot Study.
The syndrome of 'pure akinesia' and its relationship to progressive supranuclear palsy.
Transcranial brain sonography findings in two main variants of progressive supranuclear palsy.
Transcranial sonography in atypical parkinsonism: How reliable is it in real clinical practice? A multicentre comprehensive study.
Treatment of progressive supranuclear palsy with tricyclic antidepressants.
Tremor in progressive supranuclear palsy.
Volumetric analysis of the cerebellum in patients with progressive supranuclear palsy.
What can artificial neural networks teach us about neurodegenerative disorders with extrapyramidal features?
Which clinical features differentiate progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) from related disorders? A clinicopathological study.
[A 65-year-old man with Parkinsonism, gaze palsy, and dementia]
[A case of a syndrome resembling PSP after aortic arch replacement under deep hypothermic circulatory arrest].
[A clinical case of progressive supranuclear palsy with long-term frontal presentation preceding the onset of gaze palsy].
[Adult-onset dementia with abundant neurofibrillary tangles resembling progressive supranuclear palsy]
[An autopsy case of corticobasal degeneration without prominent cortical pathology--an imitator of progressive supranuclear palsy]
[Cerebral blood flow and oxygen metabolism in patients with pure akinesia and progressive supranuclear palsy]
[Clinical analysis of paralytic shellfish poisoning following ingestion of oysters]
[Contribution of oculomotor examination for the etiological diagnosis of parkinsonian syndromes]
[Corticobasal degeneration and atypical progressive supranuclear palsy: their symptomatology, laboratory examination and differential diagnosis]
[MRI diagnosis of neurodegenerative disorders]
[Partial superficial parotidectomy versus superficial parotidectomy for treatment of parotid benign tumors: evidence-based medicine analysis].
[Progressive supranuclear palsy with macular degeneration--report of three cases]
[Progressive supranuclear palsy]
[Progressive supranuclear paralysis. Quantification of dopamine D2 receptors using radionuclide tomography]
[Steele-Richardson-Olszewski syndrome]
[Successful outcome of VP shunt operation in 3 cases of idiopathic normal pressure hydrocephalus with long duration of illness]
[The genetics of corticobasal syndrome].
[Vertical oculomotor disorders in progressive supranuclear palsy and spino-cerebellar degeneration]
Paresis
Long-term results of morbidity after parotid gland surgery in benign disease.
Zolpidem in progressive supranuclear palsy.
[Partial superficial parotidectomy versus superficial parotidectomy for treatment of parotid benign tumors: evidence-based medicine analysis].
Paresthesia
Case diagnosis and characterization of suspected paralytic shellfish poisoning in Alaska.
Comparison of single-port vs. two-port VATS technique for primary spontaneous pneumothorax.
Early outcomes of single-port video-assisted thoracic surgery for primary spontaneous pneumothorax.
Incidence of chest wall paresthesia after video-assisted thoracic surgery for primary spontaneous pneumothorax.
Thalamic stimulation-evoked sensations in chronic pain patients and in nonpain (movement disorder) patients.
Uniportal vs. triportal video-assisted thoracic surgery in the treatment of primary pneumothorax-a propensity matched bicentric study.
Parkinson Disease
123I-FP-CIT in progressive supranuclear palsy and in Parkinson's disease: a SPECT semiquantitative study.
A comparison of degeneration in motor thalamus and cortex between progressive supranuclear palsy and Parkinson's disease.
A Cortical Substrate for Square-Wave Jerks in Progressive Supranuclear Palsy.
A novel diagnostic marker for progressive supranuclear palsy targeting atrophy of the subthalamic nucleus.
A systematic review of lessons learned from PET molecular imaging research in atypical parkinsonism.
Abnormal signals on proton density-weighted MRI of the superior cerebellar peduncle in progressive supranuclear palsy.
Abnormalities of optokinetic nystagmus in progressive supranuclear palsy.
Acoustical Analysis of Speech in Progressive Supranuclear Palsy.
Alexithymia and anhedonia in early Richardson's syndrome and progressive supranuclear palsy with predominant parkinsonism.
Alterations of neurotransmitter receptors and neurotransmitter transporters in progressive supranuclear palsy.
Amantadine-induced myoclonus in a patient with progressive supranuclear palsy.
An endogenous serine/threonine protein phosphatase inhibitor, G-substrate, reduces vulnerability in models of Parkinson's disease.
Apparent diffusion coefficient measurements of the middle cerebellar peduncle differentiate the Parkinson variant of MSA from Parkinson's disease and progressive supranuclear palsy.
Applause sign in Parkinsonian disorders and Huntington's disease.
Apraxia in movement disorders.
Are the International Parkinson disease and Movement Disorder Society progressive supranuclear palsy (IPMDS-PSP) diagnostic criteria accurate enough to differentiate common PSP phenotypes?
Astrocytic plaques and tufts of abnormal fibers do not coexist in corticobasal degeneration and progressive supranuclear palsy.
Atrophy in midbrain & cerebral/cerebellar pedunculi is characteristic for progressive supranuclear palsy - A double-validation whole-brain meta-analysis.
Atypical Parkinsonian syndromes: a general neurologist's perspective.
Autonomic dysfunction in patients with progressive supranuclear palsy.
Basal ganglia cholinergic and dopaminergic function in progressive supranuclear palsy.
Benzodiazepine receptors in normal human brain, in Parkinson's disease and in progressive supranuclear palsy.
Brain amino acids and glutathione in progressive supranuclear palsy.
Brain neuropeptides in progressive supranuclear palsy.
Brain somatostatin concentrations do not decrease in progressive supranuclear palsy.
Can the frontal assessment battery (FAB) differentiate bradykinetic rigid syndromes? Relation of the FAB to formal neuropsychological testing.
Cause, seasonality of death and co-morbidities in progressive supranuclear palsy (PSP).
Cerebellar dysfunction in progressive supranuclear palsy: a transcranial magnetic stimulation study.
Cholinergic cortical circuits in Parkinson's disease and in progressive supranuclear palsy: a transcranial magnetic stimulation study.
Clinical analysis of blepharospasm and apraxia of eyelid opening in patients with parkinsonism.
Clinical deficits correlate with regional cerebral atrophy in progressive supranuclear palsy.
Clinical diagnosis and diagnostic criteria of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome).
Clinical Features of Patients with Concomitant Parkinson's Disease and Progressive Supranuclear Palsy Pathology.
Clinical value of CSF amyloid-beta-42 and tau proteins in Progressive Supranuclear Palsy.
Clinical, MRI and 18F-FDG-PET/CT analysis of progressive supranuclear palsy.
Cognition in corticobasal syndrome and progressive supranuclear palsy: a review.
Cognitive dysfunction and impaired organization of complex motility in degenerative parkinsonian syndromes.
Combination of dopamine transporter and D2 receptor SPECT in the diagnostic evaluation of PD, MSA, and PSP.
Comparison of REM sleep behaviour disorder variables between patients with progressive supranuclear palsy and those with Parkinson's disease.
Conventional magnetic resonance imaging in confirmed progressive supranuclear palsy and multiple system atrophy.
Corneal Sensitivity, Blink Rate, and Corneal Nerve Density in Progressive Supranuclear Palsy and Parkinson Disease.
Correlation between qualitative balance indices, dynamic posturography and structural brain imaging in patients with progressive supranuclear palsy and its subtypes.
CSF sAPP? and sAPP? levels in Alzheimer's Disease and Multiple Other Neurodegenerative Diseases: A Network Meta-Analysis.
Cutaneous sensory and autonomic denervation in progressive supranuclear palsy.
D1 and D2-type dopamine receptors in patients with Parkinson's disease and progressive supranuclear palsy.
Decreased blood-brain barrier P-glycoprotein function in the progression of Parkinson's disease, PSP and MSA.
Deficits in long-term retention of learned motor skills in patients with cortical or subcortical degeneration.
Deterioration of horizontal saccades in progressive supranuclear palsy.
Development and assessment of sensitive immuno-PCR assays for the quantification of cerebrospinal fluid three- and four-repeat tau isoforms in tauopathies.
Development and Validation of the Automated Imaging Differentiation in Parkinsonism (AID-P): A Multi-Site Machine Learning Study.
Diagnostic accuracy of MR planimetry in clinically unclassifiable parkinsonism.
Diagnostic potential of saccadometry in progressive supranuclear palsy.
Differential diagnostic value of eye movement recording in PSP-parkinsonism, Richardson's syndrome, and idiopathic Parkinson's disease.
Differentiating PSP from MSA using MR planimetric measurements: a systematic review and meta-analysis.
Differentiation of Parkinson's disease and progressive supranuclear palsy with magnetic resonance imaging: The first Brazilian experience.
Diffusion tensor analysis of corpus callosum in progressive supranuclear palsy.
Diffusion-weighted brain imaging study of patients with clinical diagnosis of corticobasal degeneration, progressive supranuclear palsy and Parkinson's disease.
Disease course and treatment patterns in progressive supranuclear palsy: A real-world study.
Effectiveness of allied health therapy in the symptomatic management of progressive supranuclear palsy: a systematic review.
Effects of Lee Silverman Voice Treatment (LSVT LOUD) on Swallowing in Patients with Progressive Supranuclear Palsy: A Pilot Study.
Endoscopic characteristics and levodopa responsiveness of swallowing function in progressive supranuclear palsy.
Enlargements of somatosensory-evoked potentials in progressive supranuclear palsy.
Enteric GFAP expression and phosphorylation in Parkinson's disease.
Essential tremor followed by progressive supranuclear palsy: postmortem reports of 11 patients.
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases.
Executive dysfunction, behavioral changes and quality of life in Chinese patients with progressive supranuclear palsy.
Eye movement deficits in X-linked dystonia-parkinsonism are related to striatal degeneration.
Eye movements and association with regional brain atrophy in clinical subtypes of progressive supranuclear palsy.
Eyelid movement abnormalities in progressive supranuclear palsy.
Frontal atrophy correlates with behavioural changes in progressive supranuclear palsy.
Gait Analysis in Progressive Supranuclear Palsy Phenotypes.
Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study.
Guadeloupean parkinsonism: a cluster of progressive supranuclear palsy-like tauopathy.
Haplotype-specific expression of exon 10 at the human MAPT locus.
Hospitalization Rates and Comorbidities in Patients with Progressive Supranuclear Palsy in Germany from 2010 to 2017.
Hummingbird sign in progressive supranuclear palsy disease.
Hyposmia in progressive supranuclear palsy.
Immediate Effects of Sensorimotor Training in Airway Protection (smTAP) on Cough Outcomes in Progressive Supranuclear Palsy: A Feasibility Study.
Impaired perception of surface tilt in progressive supranuclear palsy.
Increased Noradrenaline as an Additional Cerebrospinal Fluid Biomarker in PSP-Like Parkinsonism.
Instability of syllable repetition in progressive supranuclear palsy.
Iron accumulation in the oculomotor nerve of the progressive supranuclear palsy brain.
Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases.
Lewy bodies in progressive supranuclear palsy represent an independent disease process.
Lifetime exposure to estrogen and progressive supranuclear palsy: Environmental and Genetic PSP study.
Limited usefulness of electroconvulsive therapy in progressive supranuclear palsy.
Local cerebral blood flow and its response to intravenous levodopa in progressive supranuclear palsy. Comparison with Parkinson's disease.
Long-term treatment with rotigotine in drug-naïve PSP patients.
Longitudinal MRI in progressive supranuclear palsy and multiple system atrophy: rates and regions of atrophy.
Metabolic network expression in parkinsonism: Clinical and dopaminergic correlations.
Micturitional disturbance in progressive supranuclear palsy.
Midbrain hypometabolism as early diagnostic sign for progressive supranuclear palsy.
Midbrain MRI assessments in progressive supranuclear palsy subtypes.
Mixing pro- and antisaccades in patients with parkinsonian syndromes.
Morning glory sign: a particular MR finding in progressive supranuclear palsy.
MR imaging of the superior profile of the midbrain: differential diagnosis between progressive supranuclear palsy and Parkinson disease.
Muscarinic receptors in the thalamus in progressive supranuclear palsy and other neurodegenerative disorders.
Natural history of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) and clinical predictors of survival: a clinicopathological study.
Neuro-ophthalmic findings in progressive supranuclear palsy.
Neurogenic bladder in progressive supranuclear palsy: A comparison with Parkinson's disease and multiple system atrophy.
Neuroimaging of PD, PSP, CBD and MSA-PET and SPECT studies.
Neuronal loss in the basal nucleus of Meynert in progressive supranuclear palsy.
Neuropsychological pattern of striatonigral degeneration: comparison with Parkinson's disease and progressive supranuclear palsy.
New and reliable MRI diagnosis for progressive supranuclear palsy.
Non motor symptoms in progressive supranuclear palsy: prevalence and severity.
Parkinson disease and progressive supranuclear palsy: protein expression in skin.
Parkinsonian syndromes associated with hydrocephalus: case reports, a review of the literature, and pathophysiological hypotheses.
Parkinsonism and dystonia caused by the illicit use of ephedrone--a longitudinal study.
Pathologic correlates of supranuclear gaze palsy with parkinsonism.
Pathological, clinical and genetic heterogeneity in progressive supranuclear palsy.
Pattern of Tau forms in CSF is altered in progressive supranuclear palsy.
Patterns of abnormal motor cortex excitability in atypical parkinsonian syndromes.
Patterns of brain atrophy in Parkinson's disease, progressive supranuclear palsy and multiple system atrophy.
Pedunculopontine tegmentum cholinergic loss leads to a progressive decline in motor abilities and neuropathological changes resembling progressive supranuclear palsy.
Persephin-overexpressing neural stem cells regulate the function of nigral dopaminergic neurons and prevent their degeneration in a model of Parkinson's disease.
Phonemic fluency quantity and quality: Comparing patients with PSP, Parkinson's disease and focal frontal and subcortical lesions.
Population based mortality and quality of death certification in progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome).
Positron emission tomography (PET) in "pure akinesia".
Possible relation of atypical parkinsonism in the French West Indies with consumption of tropical plants: a case-control study. Caribbean Parkinsonism Study Group.
Potential multisystem degeneration in Asidan patients.
Prediagnostic motor and non-motor symptoms in progressive supranuclear palsy: The step-back PSP study.
Prediction of the Clinical Severity of Progressive Supranuclear Palsy by Diffusion Tensor Imaging.
Preferential neurodegeneration in the cervical spinal cord of progressive supranuclear palsy.
Progressive supranuclear gaze palsy is in linkage disequilibrium with the tau and not the alpha-synuclein gene.
Progressive Supranuclear Palsy and Statin Use.
Progressive supranuclear palsy misdiagnosed as Parkinson's disease: a case report and review of literature.
Progressive supranuclear palsy often develops idiopathic normal pressure hydrocephalus-like magnetic resonance imaging features.
Progressive Supranuclear Palsy-Parkinsonism Predominant (PSP-P)-A Clinical Challenge at the Boundaries of PSP and Parkinson's Disease (PD).
Progressive supranuclear palsy.
Progressive supranuclear palsy. Clinical and pharmacologic update.
Progressive supranuclear palsy: a brief personalized history.
Progressive supranuclear palsy: analysis of six cases.
Progressive supranuclear palsy: MRI and pathological findings.
Progressive supranuclear palsy: neuropathologic and clinical heterogeneity.
Pure akinesia with gait freezing: a third clinical phenotype of progressive supranuclear palsy.
Quantitative evaluation of oculomotor disturbances in progressive supranuclear palsy.
Quantitative MRI measurement of superior cerebellar peduncle in progressive supranuclear palsy.
Regional brain atrophy in progressive supranuclear palsy and Lewy body disease.
Regional brain volumes distinguish PSP, MSA-P, and PD: MRI-based clinico-radiological correlations.
Rehabilitation in progressive supranuclear palsy: Effectiveness of two multidisciplinary treatments.
Role of Corpus Callosum Volumetry in Differentiating the Subtypes of Progressive Supranuclear Palsy and Early Parkinson's Disease.
Routine MRI for the differential diagnosis of Parkinson's disease, MSA, PSP, and CBD.
Sad and happy facial emotion recognition impairment in progressive supranuclear palsy in comparison with Parkinson's disease.
Sensorimotor Cough Dysfunction Is Prevalent and Pervasive in Progressive Supranuclear Palsy.
Serum adiponectin levels between patients with Parkinson's disease and those with PSP.
Shared Metabolic Profile of Caffeine in Parkinsonian Disorders.
Spatial attention and spatial short term memory in PSP and Parkinson's disease.
Speech disorders reflect differing pathophysiology in Parkinson's disease, progressive supranuclear palsy and multiple system atrophy.
Stimulation over the cerebellum with a regular figure-of-eight coil induces reduced motor cortex inhibition in patients with progressive supranuclear palsy.
Study of the rostral midbrain atrophy in progressive supranuclear palsy.
STX6 rs1411478 is not associated with increased risk of Parkinson's disease.
Subregional Pattern of Striatal Dopamine Transporter Loss on 18F FP-CIT Positron Emission Tomography in Patients With Pure Akinesia With Gait Freezing.
Tau forms in CSF as a reliable biomarker for progressive supranuclear palsy.
The auditory startle response in parkinsonism may reveal the extent but not type of pathology.
The epidemiology of PSP.
The genetic and clinico-pathological profile of early-onset progressive supranuclear palsy.
The language profile of progressive supranuclear palsy.
The Non-Motor Symptom Profile of Progressive Supranuclear Palsy.
The pattern of verbal, visuospatial and procedural learning in Richardson variant of progressive supranuclear palsy in comparison to Parkinson's disease.
The pedunculopontine nucleus in Parkinson's disease, progressive supranuclear palsy and Alzheimer's disease.
The ratio of square wave jerk rates to blink rates distinguishes progressive supranuclear palsy from Parkinson disease.
The unfolded protein response is activated in disease-affected brain regions in progressive supranuclear palsy and Alzheimer's disease.
Topography of dopamine transporter availability in progressive supranuclear palsy: a voxelwise [123I]beta-CIT SPECT analysis.
Transcranial brain sonography findings in discriminating between parkinsonism and idiopathic Parkinson disease.
Transcranial sonography for the discrimination of idiopathic Parkinson's disease from the atypical parkinsonian syndromes.
Tremor in progressive supranuclear palsy.
Tropomyosin distinguishes Lewy bodies of Parkinson disease from other neurofibrillary pathology.
Understanding the relationship between freezing of gait and other progressive supranuclear palsy features.
Untangling the tau gene association with neurodegenerative disorders.
Utility and accuracy of perceptual voice and speech distinctions in the diagnosis of Parkinson's disease, PSP and MSA-P.
Validation of mobile eye-tracking as novel and efficient means for differentiating progressive supranuclear palsy from Parkinson's disease.
Validation of the Parkinson's Disease Caregiver Burden Questionnaire in Progressive Supranuclear Palsy.
Vascular Parkinsonism: deconstructing a syndrome.
Volumetric analysis of the cerebellum in patients with progressive supranuclear palsy.
Which ante mortem clinical features predict progressive supranuclear palsy pathology?
Which clinical features differentiate progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) from related disorders? A clinicopathological study.
Whole-Brain Atrophy Differences between Progressive Supranuclear Palsy and Idiopathic Parkinson's Disease.
Whole-Brain Atrophy Rate in Idiopathic Parkinson's Disease, Multiple System Atrophy, and Progressive Supranuclear Palsy.
Word-retrieval in two cases of progressive supranuclear palsy.
[Autonomic nervous function in progressive supranuclear palsy--comparison with Parkinson's disease and healthy controls]
[Progressive supranuclear palsy : Living environment of the patients in Germany.]
[Progressive supranuclear palsy]
[Progressive supranuclear paralysis. Quantification of dopamine D2 receptors using radionuclide tomography]
[Semiquantitative evaluation of cranial computerized tomography as diagnostic support in progressive supranuclear palsy]
[Steele-Richardson-Olszewski syndrome]
Parkinson Disease, Postencephalitic
Accuracy of clinical criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome).
Parkinson's syndrome associated with neurofibrillary degeneration and tau pathologic findings.
Progressive supranuclear palsy: clinico-pathological and biochemical studies.
Progressive supranuclear palsy: new disease or variant of postencephalitic parkinsonism?
Validity and reliability of the preliminary NINDS neuropathologic criteria for progressive supranuclear palsy and related disorders.
What can artificial neural networks teach us about neurodegenerative disorders with extrapyramidal features?
Parkinsonian Disorders
'Hummingbird' Sign in a Patient with Guam Parkinsonism-Dementia Complex.
A new MR imaging index for differentiation of progressive supranuclear palsy-parkinsonism from Parkinson's disease.
A new noninvasive test to detect mitochondrial dysfunction of skeletal muscles in progressive supranuclear palsy.
A novel diagnostic marker for progressive supranuclear palsy targeting atrophy of the subthalamic nucleus.
Accuracy of a Panel of 5 Cerebrospinal Fluid Biomarkers in the Differential Diagnosis of Patients With Dementia and/or Parkinsonian Disorders.
Accuracy of the National Institute for Neurological Disorders and Stroke/Society for Progressive Supranuclear Palsy and Neuroprotection and Natural History in Parkinson Plus Syndromes Criteria for the Diagnosis of Progressive Supranuclear Palsy.
Alexithymia and anhedonia in early Richardson's syndrome and progressive supranuclear palsy with predominant parkinsonism.
An Evaluation of the Progressive Supranuclear Palsy Speech/Language Variant.
Anal sphincter EMG in the diagnosis of parkinsonian syndromes.
Aphasia in Progressive Supranuclear Palsy: As Severe as Progressive Non-Fluent Aphasia.
Applause sign in Parkinsonian disorders and Huntington's disease.
Association of PSP phenotypes with survival: A brain-bank study.
Atrophy in midbrain & cerebral/cerebellar pedunculi is characteristic for progressive supranuclear palsy - A double-validation whole-brain meta-analysis.
Atypical parkinsonian syndromes in a North African tertiary referral center.
Atypical parkinsonism on Guadeloupe, comparison with the parkinsonism-dementia complex of Guam, and environmental toxic hypotheses.
Automated Brainstem Segmentation Detects Differential Involvement in Atypical Parkinsonian Syndromes.
Automated Differential Diagnosis of Early Parkinsonism Using Metabolic Brain Networks: A Validation Study.
Automated MRI Classification in Progressive Supranuclear Palsy: a Large International Cohort Study.
Autopsy-proven progressive supranuclear palsy presenting as behavioral variant frontotemporal dementia.
Beyond the midbrain atrophy: wide spectrum of structural MRI finding in cases of pathologically proven progressive supranuclear palsy.
C9orf72 and its Relevance in Parkinsonism and Movement Disorders: A Comprehensive Review of the Literature.
Central auditory processing in parkinsonian disorders: A systematic review.
Cerebral peduncle angle: Unreliable in differentiating progressive supranuclear palsy from other neurodegenerative diseases.
Cerebrospinal fluid tau and phosphorylated tau protein are elevated in corticobasal syndrome.
Clinical analysis of blepharospasm and apraxia of eyelid opening in patients with parkinsonism.
Clinical and genetic aspects of progressive supranuclear palsy.
Clinical features differentiating patients with postmortem confirmed progressive supranuclear palsy and corticobasal degeneration.
Clinical features of dystonia in atypical parkinsonism.
Clinical genetics of familial progressive supranuclear palsy.
Clinical use of SAND battery to evaluate language in patients with Progressive Supranuclear Palsy.
Clinical Utility of 18 F-APN-1607 Tau PET Imaging in Patients with Progressive Supranuclear Palsy.
Co-morbidity of progressive supranuclear palsy and amyotrophic lateral sclerosis: a clinical-pathological case report.
Cognitive and behavioral profile of progressive supranuclear palsy and its phenotypes.
Combination of dopamine transporter and D2 receptor SPECT in the diagnostic evaluation of PD, MSA, and PSP.
Combined measurement of plasma cystatin C and low-density lipoprotein cholesterol: A valuable tool for evaluating progressive supranuclear palsy.
Comparison of clinical features in pathologically confirmed PSP and MSA patients followed at a tertiary center.
Comparison of REM sleep behaviour disorder variables between patients with progressive supranuclear palsy and those with Parkinson's disease.
Cortical atrophy differentiates Richardson's syndrome from the parkinsonian form of progressive supranuclear palsy.
Current and future treatments in progressive supranuclear palsy.
Deep learning to differentiate parkinsonian disorders separately using single midsagittal MR imaging: a proof of concept study.
Development and Validation of the Automated Imaging Differentiation in Parkinsonism (AID-P): A Multi-Site Machine Learning Study.
Diagnostic accuracy of Magnetic Resonance Parkinsonism Index in differentiating progressive supranuclear palsy from Parkinson's disease and controls in Indian patients.
Diagnostic accuracy of MR planimetry in clinically unclassifiable parkinsonism.
Diagnostic accuracy of the magnetic resonance Parkinsonism index and the midbrain-to-pontine area ratio to differentiate progressive supranuclear palsy from Parkinson's disease and the Parkinson variant of multiple system atrophy.
Diagnostic Approach to Atypical Parkinsonian Syndromes.
Diagnostic potential of automated subcortical volume segmentation in atypical parkinsonism.
Diagnostic Potential of Multimodal MRI Markers in Atypical Parkinsonian Disorders.
Different metabolic patterns analysis of Parkinsonism on the 18F-FDG PET.
Differential diagnosis of parkinsonian syndromes using F-18 fluorodeoxyglucose positron emission tomography.
Differentiating PSP from MSA using MR planimetric measurements: a systematic review and meta-analysis.
Differentiation of idiopathic Parkinson's disease, multiple system atrophy, progressive supranuclear palsy, and healthy controls using magnetization transfer imaging.
Direct analysis of tau from PSP brain identifies new phosphorylation sites and a major fragment of N-terminally cleaved tau containing four microtubule-binding repeats.
Dorsolateral nigral hyperintensity on 3.0T susceptibility-weighted imaging in neurodegenerative Parkinsonism.
Dynamic properties of horizontal and vertical eye movements in parkinsonian syndromes.
Early Impairment of Chopsticks Skills in Parkinsonism Suggests Progressive Supranuclear Palsy.
Effect of ApoE and tau on age of onset of progressive supranuclear palsy and multiple system atrophy.
Enteric GFAP expression and phosphorylation in Parkinson's disease.
Environmental Risk Factors for Progressive Supranuclear Palsy.
Epidemiology of progressive supranuclear palsy. ESGAP Consortium. European Study Group on Atypical Parkinsonisms.
Evidence for angiogenesis in Parkinson's disease, incidental Lewy body disease, and progressive supranuclear palsy.
Falls in frontotemporal dementia and related syndromes.
Familial aggregation in atypical Parkinson's disease: a case control study in multiple system atrophy and progressive supranuclear palsy.
Familial aggregation in Progressive Supranuclear Palsy and Corticobasal Syndrome.
Familial aggregation of parkinsonism in progressive supranuclear palsy.
Follow-up study of risk factors in progressive supranuclear palsy.
Freezing of gait is an early clinical feature of progressive supranuclear palsy.
FTLD-TDP and progressive supranuclear palsy in comorbidity-a report of two cases with different clinical presentations.
Functional MRI of disease progression in Parkinson disease and atypical parkinsonian syndromes.
Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study.
Genetics of Progressive Supranuclear Palsy.
Guadeloupean parkinsonism: a cluster of progressive supranuclear palsy-like tauopathy.
Hospitalization Rates and Comorbidities in Patients with Progressive Supranuclear Palsy in Germany from 2010 to 2017.
How do patients with parkinsonism present? A clinicopathological study.
How to spot ocular abnormalities in progressive supranuclear palsy? A practical review.
Imaging features associated with idiopathic normal pressure hydrocephalus have high specificity even when comparing with vascular dementia and atypical parkinsonism.
Improved language production with transcranial direct current stimulation in progressive supranuclear palsy.
Incidence of Parkinson's disease and parkinsonism in northern Sweden: a population-based study.
Increased Signal in the Superior Cerebellar Peduncle of Patients with Progressive Supranuclear Palsy.
Late-onset frontotemporal dementia associated with progressive supranuclear palsy/argyrophilic grain disease/Alzheimer's disease pathology.
Late-onset Niemann-Pick disease type C overlapping with frontotemporal dementia syndromes: a case report.
Levodopa-induced facial dystonia in a case of progressive supranuclear palsy.
Long-term follow-up of deep brain stimulation of peduncolopontine nucleus in progressive supranuclear palsy: Report of three cases.
Loss of substantia nigra hyperintensity on 7 Tesla MRI of Parkinson's disease, multiple system atrophy, and progressive supranuclear palsy.
Magnetic resonance imaging in progressive supranuclear palsy.
Magnetic resonance parkinsonism indices and interpeduncular angle in idiopathic normal pressure hydrocephalus and progressive supranuclear palsy.
Mapping of apparent susceptibility yields promising diagnostic separation of progressive supranuclear palsy from other causes of parkinsonism.
Metabolic network expression in parkinsonism: Clinical and dopaminergic correlations.
MIBG myocardial scintigraphy in progressive supranuclear palsy.
Midbrain MRI assessments in progressive supranuclear palsy subtypes.
Montreal Cognitive Assessment (MoCA) and Mini-Mental State Examination (MMSE) performance in progressive supranuclear palsy and multiple system atrophy.
Morning glory sign: a particular MR finding in progressive supranuclear palsy.
Motor programming is more affected in progressive supranuclear palsy than in Parkinson's disease: a spatiotemporal study of event-related desynchronization.
Motor, cognitive and behavioral differences in MDS PSP phenotypes.
MR findings in the substantia nigra on phase difference enhanced imaging in neurodegenerative parkinsonism.
MR imaging index for differentiation of progressive supranuclear palsy from Parkinson disease and the Parkinson variant of multiple system atrophy.
MR imaging of the superior profile of the midbrain: differential diagnosis between progressive supranuclear palsy and Parkinson disease.
MR parkinsonism index predicts vertical supranuclear gaze palsy in patients with PSP-parkinsonism.
MR planimetry in neurodegenerative parkinsonism yields high diagnostic accuracy for PSP.
MRI evaluation of progressive supranuclear palsy: differentiation from Parkinson's disease and multiple system atrophy.
MRI for the differential diagnosis of neurodegenerative parkinsonism in clinical practice.
MRI measurements predict PSP in unclassifiable parkinsonisms: A cohort study.
Mutations in bassoon in individuals with familial and sporadic progressive supranuclear palsy-like syndrome.
Neurofilament light chain level in cerebrospinal fluid can differentiate Parkinson's disease from atypical parkinsonism: Evidence from a meta-analysis.
Neurogenic bladder in progressive supranuclear palsy: A comparison with Parkinson's disease and multiple system atrophy.
Neuromelanin-sensitive magnetic resonance imaging in disease differentiation for parkinsonism or neurodegenerative disease affecting the basal ganglia.
Neuropathologic basis of frontotemporal dementia in progressive supranuclear palsy.
Neuropathological findings of PSP in the elderly without clinical PSP: Possible incidental PSP?
Neuropathology of variants of progressive supranuclear palsy.
Neuropsychological follow up in patients with Parkinson's disease, striatonigral degeneration-type multisystem atrophy, and progressive supranuclear palsy.
Neuropsychological functions in progressive supranuclear palsy, multiple system atrophy and Parkinson's disease.
Olfaction in Neuropathologically Defined Progressive Supranuclear Palsy.
Olfactory function in atypical parkinsonian syndromes.
Paraneoplastic syndrome mimicking progressive supranuclear palsy.
Parkinson's syndrome associated with neurofibrillary degeneration and tau pathologic findings.
Parkinsonian syndromes associated with hydrocephalus: case reports, a review of the literature, and pathophysiological hypotheses.
Pathologic correlates of supranuclear gaze palsy with parkinsonism.
Pathological, clinical and genetic heterogeneity in progressive supranuclear palsy.
Pathophysiology of slow vertical saccades in progressive supranuclear palsy.
Possible relation of atypical parkinsonism in the French West Indies with consumption of tropical plants: a case-control study. Caribbean Parkinsonism Study Group.
Preferential neurodegeneration in the cervical spinal cord of progressive supranuclear palsy.
Presynaptic striatal dopaminergic function in atypical parkinsonisms: A meta-analysis of imaging studies.
Prevalence of pain in atypical parkinsonism: a systematic review and meta-analysis.
Primary Tau Pathology, Not Copathology, Correlates With Clinical Symptoms in PSP and CBD.
Progression of falls in postmortem-confirmed parkinsonian disorders.
Progression of white matter damage in progressive supranuclear palsy with predominant parkinsonism.
Progressive nonfluent aphasia and subsequent aphasic dementia associated with atypical progressive supranuclear palsy pathology.
Progressive spasticity, supranuclear gaze palsy and postural instability, without parkinsonism: what's in a phenotype?
Progressive supranuclear palsy and corticobasal degeneration: lumping versus splitting.
Progressive Supranuclear Palsy and Corticobasal Degeneration: Pathophysiology and Treatment Options.
Progressive supranuclear palsy and its relation to pacific foci of the parkinsonism-dementia complex and Guadeloupean parkinsonism.
Progressive supranuclear palsy on Guam.
Progressive Supranuclear Palsy, Corticobasal Degeneration, and Multiple System Atrophy.
Progressive supranuclear palsy: a clinicopathological study of 21 cases.
Progressive supranuclear palsy: clinicopathological concepts and diagnostic challenges.
Progressive supranuclear palsy: pathology and genetics.
Pyramidal system involvement in progressive supranuclear palsy - a clinicopathological correlation.
Quantitative evaluation of oculomotor disturbances in progressive supranuclear palsy.
Retinal single-layer analysis in Parkinsonian syndromes: an optical coherence tomography study.
Role of Corpus Callosum Volumetry in Differentiating the Subtypes of Progressive Supranuclear Palsy and Early Parkinson's Disease.
Sensitivity and Specificity of Diagnostic Criteria for Progressive Supranuclear Palsy.
Sensorimotor Cough Dysfunction Is Prevalent and Pervasive in Progressive Supranuclear Palsy.
Shared Metabolic Profile of Caffeine in Parkinsonian Disorders.
Signal changes of superior cerebellar peduncle on fluid-attenuated inversion recovery in progressive supranuclear palsy.
Simple linear brainstem MRI measurements in the differential diagnosis of progressive supranuclear palsy from the parkinsonian variant of multiple system atrophy.
Specificity and sensitivity of magnetic resonance imaging findings in the diagnosis of progressive supranuclear palsy.
Speech disorders reflect differing pathophysiology in Parkinson's disease, progressive supranuclear palsy and multiple system atrophy.
Strong association of a novel Tau promoter haplotype in progressive supranuclear palsy.
Suicidal and death ideation in patients with progressive supranuclear palsy and corticobasal syndrome.
Swallow tail sign on susceptibility map-weighted imaging (SMWI) for disease diagnosing and severity evaluating in parkinsonism.
The contribution of trigemino-cervical reflexes in distinguishing progressive supranuclear palsy from multiple system atrophy.
The diagnosis of progressive supranuclear palsy: current opinions and challenges.
The Differential Diagnosis and Treatment of Atypical Parkinsonism.
The effect of repeated administrations of granulocyte colony stimulating factor for blood stem cells mobilization in patients with progressive supranuclear palsy, corticobasal degeneration and multiple system atrophy.
The language profile of progressive supranuclear palsy.
The midbrain-to-pons ratio distinguishes progressive supranuclear palsy from non-fluent primary progressive aphasias.
The Progressive Supranuclear Palsy: Past and Present Aspects.
The PSP-associated MAPT H1 subhaplotype in Guadeloupean atypical parkinsonism.
The role of 18F-FP-CIT PET in differentiation of progressive supranuclear palsy and frontotemporal dementia in the early stage.
The Role of Frontal Assessment Battery and Frontal Lobe Single-Photon Emission Computed Tomography in the Differential Diagnosis of Progressive Supranuclear Palsy Variants and Corticobasal Syndrome-A Pilot Study.
Time course of symptomatic orthostatic hypotension and urinary incontinence in patients with postmortem confirmed parkinsonian syndromes: a clinicopathological study.
Transcranial brain sonography findings in discriminating between parkinsonism and idiopathic Parkinson disease.
Transcranial sonography for the discrimination of idiopathic Parkinson's disease from the atypical parkinsonian syndromes.
Ultrasonography and MR Imaging in Progressive Supranuclear Palsy.
Undetectable specific striatal [¹²³I]-ioflupane binding in patients with parkinsonism.
Untangling the tau gene association with neurodegenerative disorders.
Validation of the Italian version of carers' quality-of-life questionnaire for parkinsonism (PQoL Carer) in progressive supranuclear palsy.
Vascular Parkinsonism: deconstructing a syndrome.
Vertical wrinkling of the forehead or Procerus sign in Progressive Supranuclear Palsy.
Which ante mortem clinical features predict progressive supranuclear palsy pathology?
Which clinical features differentiate progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) from related disorders? A clinicopathological study.
[18F-fluorodeoxyglucose positron emission tomography in Parkinson's disease]
[A 62-year-old Woman Presenting with Progressive Nonfluent Aphasia, Apraxia of Eyelid Opening, Supranuclear Gaze Palsy, and Asymmetric Rigidity].
[A 85-year-old woman with the onset of progressive gait disturbance at 80 years of the age]
[A case of progressive supranuclear palsy showing marked improvements of frontal hypoperfusion, as well as parkinsonism with amitriptyline]
[Cerebral blood flow pattern in progressive supranuclear palsy]
[Corticobasal degeneration and atypical progressive supranuclear palsy: their symptomatology, laboratory examination and differential diagnosis]
[Dopamine agonists--clinical applications beyond Parkinson's disease]
[Progressive supranuclear palsy]
Peptic Ulcer
Serum pancreatic stone protein in pancreatic diseases.
Periodontal Diseases
Numerical Evaluation of Image Contrast for Thicker and Thinner Objects among Current Intraoral Digital Imaging Systems.
Periodontitis
Identification of 3-acyl-2-phenylamino-1,4-dihydroquinolin-4-one derivatives as inhibitors of the phosphatase SerB653 in Porphyromonas gingivalis, implicated in periodontitis.
Peritonitis
Pancreatic stone protein (PSP) and pancreatitis-associated protein (PAP): a protocol of a cohort study on the diagnostic efficacy and prognostic value of PSP and PAP as postoperative markers of septic complications in patients undergoing abdominal surgery (PSP study).
Pseudomonas peritonitis in peritoneal dialysis patients: the Network #9 Peritonitis Study.
Phantom Limb
Persistent socket pain postenucleation and post evisceration: a systematic review.
Pheochromocytoma
Germ cell mitogenic activity is associated with nerve growth factor-like protein(s).
Okadaic acid induces activator protein 1 activity and immediate early gene transcription in rat pheochromocytoma cells. Mechanism of action.
phosphoglycerate dehydrogenase deficiency
3-Phosphoglycerate dehydrogenase deficiency and 3-phosphoserine phosphatase deficiency: inborn errors of serine biosynthesis.
Continuing education in neurometabolic disorders--serine deficiency disorders.
Treatment with amino acids in serine deficiency disorders.
phosphoserine phosphatase deficiency
3-Phosphoglycerate dehydrogenase deficiency and 3-phosphoserine phosphatase deficiency: inborn errors of serine biosynthesis.
Continuing education in neurometabolic disorders--serine deficiency disorders.
Erratum to: Novel Report of Phosphoserine Phosphatase Deficiency in an Adult with Myeloneuropathy and Limb Contractures.
Mutations responsible for 3-phosphoserine phosphatase deficiency.
Novel Report of Phosphoserine Phosphatase Deficiency in an Adult with Myeloneuropathy and Limb Contractures.
Phosphoserine phosphatase deficiency in a patient with Williams syndrome.
Treatment with amino acids in serine deficiency disorders.
Photophobia
Clinical implications of photophobia in progressive supranuclear palsy.
Photophobia, visual hallucinations, and REM sleep behavior disorder in progressive supranuclear palsy and corticobasal degeneration: A prospective study.
Phyllodes Tumor
Expression of serine and glycine-related enzymes in phyllodes tumor.
Pick Disease of the Brain
A comparative technetium 99m hexamethylpropylene amine oxime SPET study in different types of dementia.
A Novel MAPT Mutation, G55R, in a Frontotemporal Dementia Patient Leads to Altered Tau Function.
Accuracy of clinical criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome).
An autopsy case of frontotemporal lobar degeneration with the appearance of fused in sarcoma inclusions (basophilic inclusion body disease) clinically presenting corticobasal syndrome.
Anti-tau phospho-specific Ser262 antibody recognizes a variety of abnormal hyper-phosphorylated tau deposits in tauopathies including Pick bodies and argyrophilic grains.
Argyrophilic grain disease: a late-onset dementia with distinctive features among tauopathies.
Astrocytes expressing hyperphosphorylated tau protein without glial fibrillary tangles in argyrophilic grain disease.
Direct analysis of tau from PSP brain identifies new phosphorylation sites and a major fragment of N-terminally cleaved tau containing four microtubule-binding repeats.
Distribution of cerebral cortical lesions in corticobasal degeneration: a clinicopathological study of five autopsy cases in Japan.
Frontotemporal lobar degeneration (FTLD) concept and classification update.
High-Contrast In Vivo Imaging of Tau Pathologies in Alzheimer's and Non-Alzheimer's Disease Tauopathies.
Level of PICALM, a key component of clathrin-mediated endocytosis, is correlated with levels of phosphotau and autophagy-related proteins and is associated with tau inclusions in AD, PSP and Pick disease.
New aspects of the pathology of neurodegenerative disorders as revealed by ubiquitin antibodies.
Pick Complex: an integrative approach to frontotemporal dementia: primary progressive aphasia, corticobasal degeneration, and progressive supranuclear palsy.
Pin1 colocalization with phosphorylated tau in Alzheimer's disease and other tauopathies.
Sequential stages and distribution patterns of aging-related tau astrogliopathy (ARTAG) in the human brain.
Tau-positive fine granules in the cerebral white matter: a novel finding among the tauopathies exclusive to parkinsonism-dementia complex of Guam.
The evolution and pathology of frontotemporal dementia.
The many faces of corticobasal degeneration.
The p38 pathway is activated in Pick disease and progressive supranuclear palsy: a mechanistic link between mitogenic pathways, oxidative stress, and tau.
Ultrastructural characteristics of tau filaments in tauopathies: immuno-electron microscopic demonstration of tau filaments in tauopathies.
Validity and reliability of the preliminary NINDS neuropathologic criteria for progressive supranuclear palsy and related disorders.
What can artificial neural networks teach us about neurodegenerative disorders with extrapyramidal features?
Which clinical features differentiate progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) from related disorders? A clinicopathological study.
[Abeta, tau and alpha-synuclein and glial cells]
[Frontotemporal lobar degeneration (FTLD) - changes of its concept and classification based on aggregated proteins].
[Progressive nonfluent aphasia].
Pleural Diseases
Clinical Impact of a Pleural Unit in a Tertiary Level Hospital.
Pleural Effusion
Digital chest radiography with storage phosphor systems: potential masking of bilateral pleural effusions.
Pleural space problems after living lobar transplantation.
Pneumonia
Impact of Aspiration Pneumonia on the Clinical Course of Progressive Supranuclear Palsy: A Retrospective Cohort Study.
Natural clinical course of progressive supranuclear palsy in Chinese patients in Hong Kong.
Pneumonia caused by penicillin-non-susceptible and penicillin-susceptible pneumococci in adults: a case-control study.
Post-stroke pneumonia at the stroke unit - a registry based analysis of contributing and protective factors.
Repeated inhalation exposure of rats to an anionic high molecular weight polymer aerosol: Application of prediction models to better understand pulmonary effects and modes of action.
Risk factors for and impact of poststroke pneumonia in patients with acute ischemic stroke.
Sensorimotor Cough Dysfunction Is Prevalent and Pervasive in Progressive Supranuclear Palsy.
Pneumonia, Aspiration
A case of spinal anesthesia in a patient with progressive supranuclear palsy.
Impact of Aspiration Pneumonia on the Clinical Course of Progressive Supranuclear Palsy: A Retrospective Cohort Study.
Pneumothorax
A Mysterious Case of Spontaneous Cervical Epidural Hematoma and Bilateral Primary Spontaneous Pneumothorax Caused by a Rare Etiology.
A Mysterious Case of Spontaneous Cervical Epidural Hematoma and Bilateral Primary Spontaneous Pneumothorax caused by a Rare Etiology.
A novel dual-covering method in video-assisted thoracic surgery for pediatric primary spontaneous pneumothorax.
A Prospective Randomized Trial Comparing Manual Needle Aspiration to Closed Thoracostomy as an Initial Treatment for the First Episode of Primary Spontaneous Pneumothorax.
Abnormal Changes of a 12-Lead Electrocardiogram in Male Patients with Left Primary Spontaneous Pneumothorax.
Additional mechanical pleurodesis after thoracoscopic wedge resection and covering procedure for primary spontaneous pneumothorax.
Alveolar epithelial permeability in patients with primary spontaneous pneumothorax as determined by Tc-99m DTPA aerosol scintigraphy.
Association Between BMI and Recurrence of Primary Spontaneous Pneumothorax.
Birt-Hogg-Dube Syndrome with a Novel Mutation in the FLCN Gene.
Can CT scanning be used to select patients with unilateral primary spontaneous pneumothorax for bilateral surgery?
Cannabinoids Identification in Lung Tissues of Young Cannabis Smokers Operated for Primary Spontaneous Pneumothorax and Correlation with Pathologic Findings.
Characterisation of pleural inflammation occurring after primary spontaneous pneumothorax.
Clinical manifestations of primary spontaneous pneumothorax in pediatric patients: an analysis of 78 patients.
Clinical Profile of Spontaneous Pneumothorax in Adults: A Retrospective Study.
Comparison of single-port vs. two-port VATS technique for primary spontaneous pneumothorax.
Comparison of tracheal intubation with controlled ventilation and laryngeal mask airway with spontaneous ventilation for thoracoscopic bullectomy.
Conservative versus Interventional Treatment for Spontaneous Pneumothorax.
Correlation of Primary Spontaneous Pneumothorax and Air Pollution in Adolescents.
Data on the epidemiology, diagnosis, and treatment of patients with pneumothorax.
Do atmospheric conditions influence the first episode of primary spontaneous pneumothorax?
Evidence-based management of paediatric primary spontaneous pneumothorax.
Expression of TGF-beta receptor 1 and Smads in the tissues of primary spontaneous pneumothorax.
Factors associated with proceeding to surgical intervention and recurrence of primary spontaneous pneumothorax in adolescent patients.
Fibulin-5 Protein Is Reduced in the Lung of Patients with Spontaneous Pneumothorax Who Are Under 25 Years Old.
Fibulin-5 protein is reduced in the lung of patients with spontaneous pneumothorax who are under 25 years old.
High-Resolution CT Following Primary Spontaneous Pneumothorax in Adolescents: Useful Tool or Wasted Radiation?
How should complete lung collapse secondary to primary spontaneous pneumothorax be managed??.
Identifying Primary Spontaneous Pneumothorax from Administrative Databases: A Validation Study.
Is it a myth to perform blind apical wedge resection in primary spontaneous pneumothorax surgery to improve recurrence rates?
Multicentric Genome-Wide Association Study for Primary Spontaneous Pneumothorax.
Mutation analysis of the FLCN gene in Chinese patients with sporadic and familial isolated primary spontaneous pneumothorax.
Natural Course of Spontaneous Pneumothorax without Bullae or Blebs under High-Resolution Computed Tomography.
Pleural space problems after living lobar transplantation.
Pleurectomy versus pleural abrasion for primary spontaneous pneumothorax in children.
Pneumothorax-Time for New Guidelines?
Pneumothorax.
Prediction of recurrent spontaneous pneumothorax: CT scan findings versus management features.
Primary and Secondary Spontaneous Pneumothorax: Prevalence, Clinical Features, and In-Hospital Mortality.
Primary Spontaneous Pneumothorax Admitted in Emergency Unit: Does First Episode Differ from Recurrence? A Cross-Sectional Study.
Primary spontaneous pneumothorax in men.
Primary Spontaneous Pneumothorax in Menstruating Women Has High Recurrence.
Primary spontaneous pneumothorax-the role of the emergency observation unit.
Recurrence of primary spontaneous pneumothorax.
Recurrent primary spontaneous pneumothorax in a large Chinese family: a clinical and genetic investigation.
Risk of Primary Spontaneous Pneumothorax According to Chest Configuration.
Role of Blebs and Bullae Detected by High-Resolution Computed Tomography and Recurrent Spontaneous Pneumothorax.
Seasonal and meteorological impacts on primary spontaneous pneumothorax.
Simultaneous bilateral primary spontaneous pneumothorax.
Size of Pneumothorax can be a New Indication for Surgical Treatment in Primary Spontaneous Pneumothorax: A Prospective Study.
Small-bore catheter versus chest tube drainage for pneumothorax.
Staple line coverage with absorbable mesh after thoracoscopic bullectomy for spontaneous pneumothorax.
The clinician's perspective on pneumothorax management.
The effect of pleural abrasion on the treatment of primary spontaneous pneumothorax: a systematic review of randomized controlled trials.
The etiology and therapy of primary spontaneous pneumothoraces.
The influence of pleurodesis on the outcome of primary spontaneous pneumothorax in children.
The Size of Spontaneous Pneumothorax is a Predictor of Unsuccessful Catheter Drainage.
Thoracic Scoliosis in Patients with Primary Spontaneous Pneumothorax.
Uniportal video-assisted thoracic surgery for pneumothorax and blebs/bullae.
Video-assisted thoracoscopic surgery management of spontaneous pneumothorax - long-term results.
What is the difference in size of spontaneous pneumothorax between inspiratory and expiratory x-rays?
Will the presence of radiological signs of tension pneumothorax affect the clinical presentation of primary spontaneous pneumothorax?
[Video-assisted thoracic surgery in the treatment of spontaneous pneumothorax]
[Video-assisted thoracoscopic surgery for spontaneous pneumothorax]
Polydactyly
Reappearance of the multiple trait semilethal mutation (psp) in the fowl.
Polyneuropathies
High prevalence of false-negative anti-HTLV type I/II enzyme-linked immunosorbent assay results in HIV type 1-positive patients.
Prevalence and Characteristics of Polyneuropathy in Atypical Parkinsonian Syndromes: An Explorative Study.
Polyradiculoneuropathy
[Clinical analysis of paralytic shellfish poisoning following ingestion of oysters]
Pressure Ulcer
Exploring the challenge of health research priority setting in partnership: reflections on the methodology used by the James Lind Alliance Pressure Ulcer Priority Setting Partnership.
Primary Dysautonomias
Atypical parkinsonism in Guadeloupe: a common risk factor for two closely related phenotypes?
Comparison of natural histories of progressive supranuclear palsy and multiple system atrophy.
Electrophysiological and clinical assessment of dysautonomia in multiple system atrophy (MSA) and progressive supranuclear palsy (PSP): a comparative study.
Predictors of survival in progressive supranuclear palsy and multiple system atrophy: a systematic review and meta-analysis.
Predominant cortical dysfunction in Guadeloupean parkinsonism.
Primary Progressive Nonfluent Aphasia
Are frontotemporal lobar degeneration, progressive supranuclear palsy and corticobasal degeneration distinct diseases?
Progressive nonfluent aphasia and subsequent aphasic dementia associated with atypical progressive supranuclear palsy pathology.
Prolactinoma
Pituitary tumors contain a side population with tumor stem cell-associated characteristics.
Prostatic Neoplasms
Chemopreventive effect of PSP through targeting of prostate cancer stem cell-like population.
Comparison of prostate secretory protein with prostate specific antigen and prostatic acid phosphatase as a serum biomarker for diagnosis and monitoring patients with prostate carcinoma.
Polysaccharopeptide enhanced the anti-cancer effect of gamma-tocotrienol through activation of AMPK.
Procyanidin from peanut skin induces antiproliferative effect in human prostate carcinoma cells DU145.
Recent Advances and Challenges in Studies of Control of Cancer Stem Cells and the Gut Microbiome by the Trametes-Derived Polysaccharopeptide PSP (Review).
Therapeutic effects of human monoclonal PSMA antibody-mediated TRIM24 siRNA delivery in PSMA-positive castration-resistant prostate cancer.
Two-site monoclonal antibody-based immunoradiometric assay for measuring prostate secretory protein in serum.
Zoledronic acid in combination with serine/threonine phosphatase inhibitors induces enhanced cytotoxicity and apoptosis in hormone-refractory prostate cancer cell lines by decreasing the activities of PP1 and PP2A.
Prostatitis
Evaluation of seminal plasma parameters in patients with chronic prostatitis or leukocytospermia.
Proteinuria
In vitro immunoglobulin production by peripheral blood mononuclear cells as a prognostic factor in IgA nephropathy.
Renal glomerular changes associated with liver cirrhosis.
[Incidence, etiology and prognostic value of persistent significant proteinuria in kidney transplants]
Pseudobulbar Palsy
Progressive supranuclear palsy: a clinicopathological study of 21 cases.
Progressive Supranuclear Palsy: What do we know About it?
The Progressive Supranuclear Palsy: Past and Present Aspects.
[Palilalia associated with progressive supranuclear palsy]
[Progressive supranuclear palsy]
[Widespread argentophilic structures in progressive supranuclear palsy--an autopsy case report]
Psoriasis
Patient Support Program Increased Medication Adherence with Lower Total Health Care Costs Despite Increased Drug Spending.
Psychomotor Agitation
Restless legs syndrome, leg motor restlessness and their variants in patients with Parkinson's disease and related disorders.
Pulmonary Atelectasis
Complete atelectasis of the lung in patients with primary spontaneous pneumothorax.
Conservative management of a complete primary spontaneous pneumothorax.
How should complete lung collapse secondary to primary spontaneous pneumothorax be managed??.
The incidence and risk factors of asymptomatic primary spontaneous pneumothorax detected during health check-ups.
Uniportal video assisted thoracoscopic surgery bullectomy and double pleurodesis for primary spontaneous pneumothorax.
Pulmonary Disease, Chronic Obstructive
Clinical Profile of Spontaneous Pneumothorax in Adults: A Retrospective Study.
Neural control of pressure support ventilation improved patient-ventilator synchrony in patients with different respiratory system mechanical properties: a prospective, crossover trial.
Neural versus pneumatic control of pressure support in patients with chronic obstructive pulmonary diseases at different levels of positive end expiratory pressure: a physiological study.
Small-bore catheter versus chest tube drainage for pneumothorax.
Rectal Prolapse
Functional outcome after perineal stapled prolapse resection for external rectal prolapse.
Perineal stapled prolapse resection for full thickness external rectal prolapse: a multicentre prospective study.
[Operative therapy of external rectal prolapse with a stapler].
Reflex, Abnormal
Comparison of natural histories of progressive supranuclear palsy and multiple system atrophy.
REM Sleep Behavior Disorder
Photophobia, visual hallucinations, and REM sleep behavior disorder in progressive supranuclear palsy and corticobasal degeneration: A prospective study.
Progressive supranuclear palsy is not associated with neurogenic orthostatic hypotension.
Renal Insufficiency, Chronic
A validation of presepsin levels in kidney dysfunction patients: four case reports.
Respiratory Insufficiency
Alterations of 3,4-dihydroxyphenylethylamine and its metabolite 3,4-dihydroxyphenylacetic produced in rat brain tissues after systemic administration of saxitoxin.
New setting of neurally adjusted ventilatory assist for noninvasive ventilation by facial mask: a physiologic study.
[Clinical analysis of paralytic shellfish poisoning following ingestion of oysters]
Respiratory Paralysis
Shellfish contamination with marine biotoxins in Portugal and spring tides: a dangerous health coincidence.
Respiratory Tract Infections
Cause, seasonality of death and co-morbidities in progressive supranuclear palsy (PSP).
Retinal Degeneration
Drosophila retinal degeneration C (rdgC) encodes a novel serine/threonine protein phosphatase.
Molecular cloning, expression, and characterization of a novel human serine/threonine protein phosphatase, PP7, that is homologous to Drosophila retinal degeneration C gene product (rdgC).
Regulatory arrestin cycle secures the fidelity and maintenance of the fly photoreceptor cell.
Rhinitis, Allergic
Polypoid Change of the Middle Turbinate and Paranasal Sinus Polyposis Are Distinct Entities.
Root Resorption
Comparison of cone-beam computed tomography with intraoral photostimulable phosphor imaging plate for diagnosis of endodontic complications: a simulation study.
Diagnosis of artificially induced external root resorption using conventional intraoral film radiography, CCD, and PSP: an ex vivo study.
Diagnosis of Simulated External Root Resorption Using Conventional Intraoral Film Radiography, CCD, PSP, and CBCT: A Comparison Study.
Diagnostic Accuracy of Charge-coupled Device Sensor and Photostimulable Phosphor Plate Receptor in the Detection of External Root Resorption In Vitro.
Sarcoma
In vivo antioxidant, hypoglycemic, and anti-tumor activities of anthocyanin extracts from purple sweet potato.
Scoliosis
A comparison between the Cotrel-Dubousset and the pedicle screw-plate instrumentations in the adolescent idiopathic scoliosis.
Joint and skeletal deformities in Parkinson's disease, multiple system atrophy, and progressive supranuclear palsy.
Thoracic Scoliosis in Patients with Primary Spontaneous Pneumothorax.
Seizures
Lesion of the tuberomammillary nucleus E2-region attenuates postictal seizure protection in rats.
Seizure prevalence in neurodegenerative diseases-a study of autopsy proven cases.
Seizures in progressive supranuclear palsy.
Tau-Induced Pathology in Epilepsy and Dementia: Notions from Patients and Animal Models.
Sepsis
A validation of presepsin levels in kidney dysfunction patients: four case reports.
Concomitant assessment of PSP and NT-proCNP as predictive markers of sepsis in severe trauma patients under mechanical ventilation.
Expression of Pancreatic Stone Protein is Unaffected by Trauma and Subsequent Surgery in Burn Patients.
Incidence and Time Point of Sepsis Detection as Related to Different Sepsis Definitions in Severely Burned Patients and Their Accompanying Time Course of Pro-Inflammatory Biomarkers.
Measurement of pancreatic stone protein in the identification and management of sepsis.
Pancreatic stone protein (PSP) and pancreatitis-associated protein (PAP): a protocol of a cohort study on the diagnostic efficacy and prognostic value of PSP and PAP as postoperative markers of septic complications in patients undergoing abdominal surgery (PSP study).
Pancreatic stone protein - sepsis and the riddles of the exocrine pancreas.
Pancreatic stone protein and soluble CD25 for infection and sepsis in an emergency department.
Pancreatic Stone Protein Predicts Sepsis in Severely Burned Patients Irrespective of Trauma Severity: A Monocentric Observational Study.
Prognostic performance of pancreatic stone protein in critically ill patients with sepsis.
Prognostic Value of High-Sensitivity C-Reactive Protein, Procalcitonin and Pancreatic Stone Protein in Pediatric Sepsis.
Prognostication of Mortality in Critically Ill Patients With Severe Infections.
Response of routine inflammatory biomarkers and novel Pancreatic Stone Protein to inhalation injury and its interference with sepsis detection in severely burned patients.
Sepsis biomarkers in unselected patients on admission to intensive or high-dependency care.
Serial measurement of pancreatic stone protein for the early detection of sepsis in intensive care unit patients: a prospective multicentric study.
The pancreas responds to remote damage and systemic stress by secretion of the pancreatic secretory proteins PSP/regI and PAP/regIII.
The Role of Pancreatic Stone Protein in Diagnosis of Early Onset Neonatal Sepsis.
Wip 1 inhibits intestinal inflammation in inflammatory bowel disease.
[Inflammation markers and bloodstream infection (review of literature).]
[Value of Procalcitonin, High Sensitivity C-reactive Protein and Pancreatic Stone Protein in Predicting Prognosis of Children with Sepsis].
Shock, Septic
Prognostication of Mortality in Critically Ill Patients With Severe Infections.
Shoulder Pain
Poststroke Pain.
Sick Sinus Syndrome
[Various diagnostic criteria for abnormal signs of the artificial pacemaker examined by transesophageal electric stimulation of the left atrium]
Sleep Apnea Syndromes
Polysomnographic findings, video-based sleep analysis and sleep perception in progressive supranuclear palsy.
Predicting poor school performance in children suspected for sleep-disordered breathing.
Sleep Deprivation
Rest-activity rhythm disruption in progressive supranuclear palsy.
Sleepless Night and Day, the Plight of Progressive Supranuclear Palsy.
Sleep Initiation and Maintenance Disorders
Sleep Disorders in Atypical Parkinsonism.
Sleep Quality and Mental Disorder Symptoms among Canadian Public Safety Personnel.
Solitary Fibrous Tumors
Huge Pulmonary Sclerosing Pneumocytoma with Endobronchial Invasion: A Case Report with a Literature Review.
Solitary Pulmonary Nodule
Pulmonary sclerosing pneumocytoma mimicking lung cancer: Case report and review of the literature.
Speech Disorders
Motor Speech Disorders and Communication Limitations in Progressive Supranuclear Palsy.
[Parkinsonism-associated speech disorders].
Spinal Diseases
How do patients with parkinsonism present? A clinicopathological study.
Spinocerebellar Degenerations
An autopsied case of progressive supranuclear palsy presenting with cerebellar ataxia and severe cerebellar involvement.
Progressive Supranuclear Palsy with Predominant Cerebellar Ataxia.
[An autopsied case of progressive supranuclear palsy, initially diagnosed as spinocerebellar degeneration with severe olivopontocerebellar involvement].
Spondylitis, Ankylosing
Patient Support Program Increased Medication Adherence with Lower Total Health Care Costs Despite Increased Drug Spending.
ST Elevation Myocardial Infarction
Presepsin (sCD14-ST): could it be a novel marker for the diagnosis of ST elevation myocardial infarction?
Starvation
Effect of intravenous feeding on wound healing in starvation: an experimental study on the rabbit.
Role of an Escherichia coli stress-response operon in stationary-phase survival.
Stomach Neoplasms
A review of research on the protein-bound polysaccharide (polysaccharopeptide, PSP) from the mushroom Coriolus versicolor (Basidiomycetes: Polyporaceae).
[Resection of gastric carcinoma with preserving of the spleen and pancreas and functional clearance lymph nodes of the spleen hillus and splenic artery]
Striatonigral Degeneration
Combination of dopamine transporter and D2 receptor SPECT in the diagnostic evaluation of PD, MSA, and PSP.
Magnetic resonance imaging distinguishes progressive supranuclear palsy from multiple system atrophy.
Progressive supranuclear palsy: MRI and pathological findings.
Stroke
A comparison of tau protein in cerebrospinal fluid between corticobasal degeneration and progressive supranuclear palsy.
Accuracy of the National Institute for Neurological Disorders and Stroke/Society for Progressive Supranuclear Palsy and Neuroprotection and Natural History in Parkinson Plus Syndromes Criteria for the Diagnosis of Progressive Supranuclear Palsy.
Are the International Parkinson disease and Movement Disorder Society progressive supranuclear palsy (IPMDS-PSP) diagnostic criteria accurate enough to differentiate common PSP phenotypes?
Association between nasogastric tubes, pneumonia, and clinical outcomes in acute stroke patients.
Atrophy in midbrain & cerebral/cerebellar pedunculi is characteristic for progressive supranuclear palsy - A double-validation whole-brain meta-analysis.
Case Report: Barely Able to Speak, Can't Stop Echoing: Echolalic Dynamic Aphasia in Progressive Supranuclear Palsy.
Characterizing swallowing abnormalities in progressive supranuclear palsy.
Clinical heterogeneity in progressive supranuclear palsy: Problems of clinical diagnostic criteria of NINDS-SPSP in a retrospective study of seven Japanese autopsy cases.
Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): report of the NINDS-SPSP international workshop.
Cough reflex attenuation and swallowing dysfunction in sub-acute post-stroke patients: prevalence, risk factors, and clinical outcome.
Diagnostic accuracy of Magnetic Resonance Parkinsonism Index in differentiating progressive supranuclear palsy from Parkinson's disease and controls in Indian patients.
Diagnostic validity of magnetic resonance parkinsonism index in differentiating patients with progressive supranuclear palsy from patients with Parkinson's disease.
Effects of cerebral ischemia in mice deficient in Persephin.
Familial aggregation of parkinsonism in progressive supranuclear palsy.
Freezing of gait is an early clinical feature of progressive supranuclear palsy.
Gait analysis in PSP and NPH: Dual-task conditions make the difference.
Post-stroke pneumonia at the stroke unit - a registry based analysis of contributing and protective factors.
Progression of dysarthria and dysphagia in postmortem-confirmed parkinsonian disorders.
Progression of falls in postmortem-confirmed parkinsonian disorders.
Progressive supranuclear palsy combined with Alzheimer's disease: A clinicopathological study of two autopsy cases.
Progressive supranuclear palsy in a sample of Brazilian population: clinical features of 16 patients.
Progressive supranuclear palsy with wall-eyed bilateral internuclear ophthalmoplegia syndrome.
Progressive supranuclear palsy.
Risk factors for and impact of poststroke pneumonia in patients with acute ischemic stroke.
Risk factors for progressive supranuclear palsy.
Risk stratification model for post-stroke pneumonia in patients with acute ischemic stroke.
Specificity and sensitivity of magnetic resonance imaging findings in the diagnosis of progressive supranuclear palsy.
Urinary Dysfunction in Progressive Supranuclear Palsy Compared with Other Parkinsonian Disorders.
Usefulness of the Neutrophil-to-Lymphocyte Ratio as a Predictor of Pneumonia and Urinary Tract Infection Within the First Week After Acute Ischemic Stroke.
Vascular Parkinsonism: deconstructing a syndrome.
Vascular progressive supranuclear palsy.
[Echocardiographic evaluation of mitral stenosis: significance of Pc-To/Ac-Mo ratio (author's transl)]
Subacute Sclerosing Panencephalitis
Descriptive epidemiology of some rare neurological diseases in Benghazi, Libya.
Subclavian Steal Syndrome
Progressive supranuclear palsy in the course of subclavian steal syndrome.
Supranuclear Palsy, Progressive
A new noninvasive test to detect mitochondrial dysfunction of skeletal muscles in progressive supranuclear palsy.
Accuracy of clinical criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome).
Accuracy of clinical diagnosis of progressive supranuclear palsy.
Accuracy of the National Institute for Neurological Disorders and Stroke/Society for Progressive Supranuclear Palsy and Neuroprotection and Natural History in Parkinson Plus Syndromes Criteria for the Diagnosis of Progressive Supranuclear Palsy.
Alexithymia and anhedonia in early Richardson's syndrome and progressive supranuclear palsy with predominant parkinsonism.
An Evaluation of the Progressive Supranuclear Palsy Speech/Language Variant.
Anti-tau phospho-specific Ser262 antibody recognizes a variety of abnormal hyper-phosphorylated tau deposits in tauopathies including Pick bodies and argyrophilic grains.
APOE E4 is a determinant for Alzheimer type pathology in progressive supranuclear palsy.
Are the International Parkinson disease and Movement Disorder Society progressive supranuclear palsy (IPMDS-PSP) diagnostic criteria accurate enough to differentiate common PSP phenotypes?
Assessment of 18F-PI-2620 as a Biomarker in Progressive Supranuclear Palsy.
Assessment of midbrain atrophy in patients with progressive supranuclear palsy with routine magnetic resonance imaging.
Association of an extended haplotype in the tau gene with progressive supranuclear palsy.
Association of Progressive Supranuclear Palsy Rating Scale with Progressive Supranuclear Palsy Quality of Life Scale.
Association of PSP phenotypes with survival: A brain-bank study.
Association of Tripartite Motif Containing 11 rs564309 with Tau Pathology in Progressive Supranuclear Palsy.
Automated Brainstem Segmentation Detects Differential Involvement in Atypical Parkinsonian Syndromes.
Autopsy-proven progressive supranuclear palsy presenting as behavioral variant frontotemporal dementia.
Balance and eye movement training to improve gait in people with progressive supranuclear palsy: quasi-randomized clinical trial.
Behavioral changes as the earliest clinical manifestation of progressive supranuclear palsy.
Blood-based NfL: A biomarker for differential diagnosis of parkinsonian disorder.
Blood-Brain Barrier Dysfunction as a Hallmark Pathology in Chronic Traumatic Encephalopathy.
Can the frontal assessment battery (FAB) differentiate bradykinetic rigid syndromes? Relation of the FAB to formal neuropsychological testing.
Caregiver strain in progressive supranuclear palsy and corticobasal syndromes.
Caregiving in progressive supranuclear palsy.
Cerebral blood flow in corticobasal degeneration and progressive supranuclear palsy.
Cerebral oxygen metabolism in patients with progressive supranuclear palsy: a positron emission tomography study.
Characteristics and progression of cognitive deficits in progressive supranuclear palsy vs. multiple system atrophy and Parkinson's disease.
Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism.
Cholinergic cortical circuits in Parkinson's disease and in progressive supranuclear palsy: a transcranial magnetic stimulation study.
Clinical correlates of longitudinal brain atrophy in progressive supranuclear palsy.
Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria.
Clinical features and natural history of progressive supranuclear palsy: a clinical cohort study.
Clinical features of dystonia in atypical parkinsonism.
Clinical Features of Patients with Concomitant Parkinson's Disease and Progressive Supranuclear Palsy Pathology.
Clinical outcomes of two main variants of progressive supranuclear palsy and multiple system atrophy: a prospective natural history study.
Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): report of the NINDS-SPSP international workshop.
Clinical use of SAND battery to evaluate language in patients with Progressive Supranuclear Palsy.
Clinical value of CSF amyloid-beta-42 and tau proteins in Progressive Supranuclear Palsy.
Cognitive and behavioral profile of progressive supranuclear palsy and its phenotypes.
Cognitive decline on the Repeatable Battery for the Assessment of Neuropsychological Status in progressive supranuclear palsy.
Cognitive deficits in progressive supranuclear palsy on the Repeatable Battery for the Assessment of Neuropsychological Status.
Cognitive disturbances in progressive supranuclear palsy.
Cognitive impairment in progressive supranuclear palsy-Richardson's syndrome is related to white matter damage.
Combination of dopamine transporter and D2 receptor SPECT in the diagnostic evaluation of PD, MSA, and PSP.
Conventional magnetic resonance imaging in confirmed progressive supranuclear palsy and multiple system atrophy.
Cortical Alzheimer Type Pathology Does Not Influence tau Pathology in Progressive Supranuclear Palsy.
Cortical atrophy differentiates Richardson's syndrome from the parkinsonian form of progressive supranuclear palsy.
CSF sAPP? and sAPP? levels in Alzheimer's Disease and Multiple Other Neurodegenerative Diseases: A Network Meta-Analysis.
Davunetide in patients with progressive supranuclear palsy: a randomised, double-blind, placebo-controlled phase 2/3 trial.
Deciphering the saccade velocity profile of progressive supranuclear palsy: A sign of latent cerebellar/brainstem dysfunction?
DescribePSP and ProPSP: German Multicenter Networks for Standardized Prospective Collection of Clinical Data, Imaging Data, and Biomaterials of Patients With Progressive Supranuclear Palsy.
Development and Validation of the Automated Imaging Differentiation in Parkinsonism (AID-P): A Multi-Site Machine Learning Study.
Diagnosis and management of progressive supranuclear palsy.
Differential diagnostic value of eye movement recording in PSP-parkinsonism, Richardson's syndrome, and idiopathic Parkinson's disease.
Differentiation of neurodegenerative parkinsonian syndromes by volumetric magnetic resonance imaging analysis and support vector machine classification.
Difficulties in the diagnosis of four repeats (4R) tauopathic parkinsonian syndromes.
Distribution of tuft-shaped astrocytes in the cerebral cortex in progressive supranuclear palsy.
Effect of MAPT and APOE on prognosis of progressive supranuclear palsy.
Electrophysiological features of lower motor neuron involvement in progressive supranuclear palsy.
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases.
Executive dysfunction is the primary cognitive impairment in progressive supranuclear palsy.
Eye movements and association with regional brain atrophy in clinical subtypes of progressive supranuclear palsy.
Factors associated with development and distribution of granular/fuzzy astrocytes in neurodegenerative diseases.
Familial progressive supranuclear palsy: detection of subclinical cases using 18F-dopa and 18fluorodeoxyglucose positron emission tomography.
Feasibility of short imaging protocols for [18F]PI-2620 tau-PET in progressive supranuclear palsy.
Frontal presentation in progressive supranuclear palsy.
Further extension of the H1 haplotype associated with progressive supranuclear palsy.
Gait Analysis in Progressive Supranuclear Palsy Phenotypes.
Gait analysis in PSP and NPH: Dual-task conditions make the difference.
Health-related quality of life in patients with progressive supranuclear palsy.
Human positron emission tomographic [18F]fluorodopa studies correlate with dopamine cell counts and levels.
Impairment of eyeblink classical conditioning in progressive supranuclear palsy.
In vivo comparison of Richardson's syndrome and progressive supranuclear palsy-parkinsonism.
In vivo evaluation of white matter pathology in patients of progressive supranuclear palsy using TBSS.
Increased Signal in the Superior Cerebellar Peduncle of Patients with Progressive Supranuclear Palsy.
Inferior olivary hypertrophy is uncommon in progressive supranuclear palsy.
Interhemispheric inhibition in different phenotypes of progressive supranuclear palsy.
Lack of trigemino-cervical reflexes in progressive supranuclear palsy.
Levodopa-induced facial dystonia in a case of progressive supranuclear palsy.
Lifetime exposure to estrogen and progressive supranuclear palsy: Environmental and Genetic PSP study.
Locus coeruleus pathology in progressive supranuclear palsy, and its relation to disease severity.
Long-term treatment with rotigotine in drug-naïve PSP patients.
Magnetic resonance imaging distinguishes progressive supranuclear palsy from multiple system atrophy.
Measuring quality of life in PSP: the PSP-QoL.
Metabolic network expression in parkinsonism: Clinical and dopaminergic correlations.
Microtubule-associated protein tau genetic variations are uncommon cause of frontotemporal dementia in south India.
Midbrain atrophy is not a biomarker of progressive supranuclear palsy pathology.
Midbrain catecholaminergic neurons co-express ?-synuclein and tau in progressive supranuclear palsy.
Midbrain MRI assessments in progressive supranuclear palsy subtypes.
Mild Cognitive Impairment and Progression to Dementia in Progressive Supranuclear Palsy.
Motor, cognitive and behavioral differences in MDS PSP phenotypes.
MRI gray and white matter measures in progressive supranuclear palsy and corticobasal syndrome.
Natural history of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) and clinical predictors of survival: a clinicopathological study.
Neurofibrillary tangles in progressive supranuclear palsy contain the same tau epitopes identified in Alzheimer's disease PHFtau.
Neuroimaging of PD, PSP, CBD and MSA-PET and SPECT studies.
Neuroimaging-pathological correlations of [18F]THK5351 PET in progressive supranuclear palsy.
Neuropathologic basis of frontotemporal dementia in progressive supranuclear palsy.
New and reliable MRI diagnosis for progressive supranuclear palsy.
Obsessive compulsive personality disorder in Progressive Supranuclear Palsy, Multiple System Atrophy and Essential Tremor.
Parkinsonian syndromes associated with hydrocephalus: case reports, a review of the literature, and pathophysiological hypotheses.
Patterns of brain atrophy in Parkinson's disease, progressive supranuclear palsy and multiple system atrophy.
Pedunculopontine Nucleus Deep Brain Stimulation for Parkinsonian Disorders: A Case Series.
Population based mortality and quality of death certification in progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome).
Potential multisystem degeneration in Asidan patients.
Prediagnostic motor and non-motor symptoms in progressive supranuclear palsy: The step-back PSP study.
Predicting alpha-synuclein pathology by REM sleep behavior disorder diagnosis.
Preliminary studies of differential impairments of the dopaminergic system in subtypes of progressive supranuclear palsy.
Prevalence and Characteristics of Polyneuropathy in Atypical Parkinsonian Syndromes: An Explorative Study.
Progression of gait, speech and swallowing deficits in progressive supranuclear palsy.
Progression of two Progressive Supranuclear Palsy phenotypes with comparable initial disability.
Progression of white matter damage in progressive supranuclear palsy with predominant parkinsonism.
Progressive nonfluent aphasia and subsequent aphasic dementia associated with atypical progressive supranuclear palsy pathology.
Progressive Supranuclear Gaze Palsy with Predominant Cerebellar Ataxia: A Case Series with Videos.
Progressive supranuclear palsy (PSP): Richardson syndrome and other PSP variants.
Progressive supranuclear palsy with dementia: cortical pathology.
Progressive supranuclear palsy with wall-eyed bilateral internuclear ophthalmoplegia syndrome.
Progressive supranuclear palsy.
Progressive supranuclear palsy: a survey of the disease course.
Progressive supranuclear palsy: neuropathologic and clinical heterogeneity.
Progressive supranuclear palsy: new disease or variant of postencephalitic parkinsonism?
Pyramidal system involvement in progressive supranuclear palsy - a clinicopathological correlation.
Quantitative evaluation of oculomotor disturbances in progressive supranuclear palsy.
Quantitative MRI measurement of superior cerebellar peduncle in progressive supranuclear palsy.
Quantitative proteomics identifies surfactant-resistant alpha-synuclein in cerebral cortex of parkinsonism-dementia complex of Guam but not alzheimer's disease or progressive supranuclear palsy.
Radiological biomarkers for diagnosis in PSP: Where are we and where do we need to be?
Rate of decline in progressive supranuclear palsy.
Research goals in progressive supranuclear palsy. First International Brainstorming Conference on PSP.
Retinal degeneration in progressive supranuclear palsy measured by optical coherence tomography and scanning laser polarimetry.
Reversible progressive supranuclear palsy-like phenotype as an initial manifestation of HIV infection.
Salivary alpha-synuclein in the diagnosis of Parkinson's disease and Progressive Supranuclear Palsy.
Selective decrease of large neurons in the neostriatum in progressive supranuclear palsy.
Sensitivity and Specificity of Diagnostic Criteria for Progressive Supranuclear Palsy.
Side effects induced by the acute levodopa challenge in Parkinson's Disease and atypical parkinsonisms.
Sleep disturbances in the speech-language variant of progressive supranuclear palsy.
Speech disorders reflect differing pathophysiology in Parkinson's disease, progressive supranuclear palsy and multiple system atrophy.
Spinal cord stimulation therapy for gait dysfunction in progressive supranuclear palsy patients.
Structural and functional meta-analytic evidence for fronto-subcortical system deficit in progressive supranuclear palsy.
Subcortical damage and cortical dysfunction in progressive supranuclear palsy demonstrated by positron emission tomography.
Substantia nigra echogenicity in progressive supranuclear palsy.
The auditory startle response in parkinsonism may reveal the extent but not type of pathology.
The Cure PSP Care Guide: A Telephonic Nursing Intervention for Individuals and Families Living With Progressive Supranuclear Palsy.
The Dementia Rating Scale in Alzheimer's disease, Huntington's disease and progressive supranuclear palsy.
The diagnosis of neurodegenerative disorders based on clinical and pathological findings using an MRI approach.
The H1c haplotype at the MAPT locus is associated with Alzheimer's disease.
The language profile of progressive supranuclear palsy.
The phenotypic spectrum of progressive supranuclear palsy: a retrospective multicenter study of 100 definite cases.
The ratio of square wave jerk rates to blink rates distinguishes progressive supranuclear palsy from Parkinson disease.
The Role of Frontal Assessment Battery and Frontal Lobe Single-Photon Emission Computed Tomography in the Differential Diagnosis of Progressive Supranuclear Palsy Variants and Corticobasal Syndrome-A Pilot Study.
Transcranial brain sonography findings in two main variants of progressive supranuclear palsy.
Treatment of progressive supranuclear palsy with tricyclic antidepressants.
Tremor in progressive supranuclear palsy.
Utility of Frontal Assessment Battery in detection of neuropsychological dysfunction in Richardson variant of progressive supranuclear palsy.
Variation at the TRIM11 Locus Modifies Progressive Supranuclear Palsy Phenotype.
Volumetric analysis of the cerebellum in patients with progressive supranuclear palsy.
What can artificial neural networks teach us about neurodegenerative disorders with extrapyramidal features?
Which ante mortem clinical features predict progressive supranuclear palsy pathology?
Which clinical features differentiate progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) from related disorders? A clinicopathological study.
[A 65-year-old man with Parkinsonism, gaze palsy, and dementia]
[Adult-onset dementia with abundant neurofibrillary tangles resembling progressive supranuclear palsy]
[MRI diagnosis of neurodegenerative disorders]
[Progressive supranuclear palsy-Richardson syndrome with visual attention disturbance (Holmes and Horrax) and ataxie optique (Garcin): a case report].
[Progressive supranuclear paralysis. Quantification of dopamine D2 receptors using radionuclide tomography]
[The genetics of corticobasal syndrome].
Sweating, Gustatory
A meta-analysis of the pros and cons of partial superficial parotidectomy versus superficial parotidectomy for the treatment of benign parotid neoplasms.
Superficial or partial superficial parotidectomy for the treatment of primary benign parotid tumors.
Superficial parotidectomy versus partial superficial parotidectomy in treating benign parotid tumors.
Superficial parotidectomy versus retrograde partial superficial parotidectomy in treating benign salivary gland tumor (pleomorphic adenoma).
[Partial superficial parotidectomy versus superficial parotidectomy for treatment of parotid benign tumors: evidence-based medicine analysis].
[Sixty-two cases report of surgical treatment of parotid pleomorphic adenoma]
Syndactyly
Reappearance of the multiple trait semilethal mutation (psp) in the fowl.
Synucleinopathies
Cerebrospinal fluid neurofilament light and tau protein as mortality biomarkers in parkinsonism.
Diagnostic Approach to Atypical Parkinsonian Syndromes.
Glucocerebrosidase mutations in primary parkinsonism.
Pathologic changes of progressive supranuclear palsy, corticobasal degeneration, and multiple system atrophy : Prototype and clinicopathological diversity.
Quantitative proteomics identifies surfactant-resistant alpha-synuclein in cerebral cortex of parkinsonism-dementia complex of Guam but not alzheimer's disease or progressive supranuclear palsy.
Reduced alpha-synuclein in cerebrospinal fluid in synucleinopathies: evidence from a meta-analysis.
Serum adiponectin levels between patients with Parkinson's disease and those with PSP.
Tachycardia
Failing Left Ventricles Have an Enhanced Post-Stimulation Potentiation Despite Their Impaired Force Frequency Relationship.
Mechanical function and substrate oxidation in the neonatal pig heart subjected to pacing-induced tachycardia.
Performance of the neonatal pig heart subjected to oxygen insufficiency.
Tachycardia, Sinus
Left stellate ganglion and vagal nerve activity and cardiac arrhythmias in ambulatory dogs with pacing-induced congestive heart failure.
Tachycardia, Ventricular
Prolonged Sinus Pauses upon Termination of Paroxysmal Atrial Fibrillation: Abnormal Right Atrial Electrophysiologic and Electroanatomic Findings.
Tauopathies
4-repeat tauopathy sharing pathological and biochemical features of corticobasal degeneration and progressive supranuclear palsy.
A Novel MAPT Mutation, G55R, in a Frontotemporal Dementia Patient Leads to Altered Tau Function.
ABI3 and PLCG2 missense variants as risk factors for neurodegenerative diseases in Caucasians and African Americans.
Aphasia in Progressive Supranuclear Palsy: As Severe as Progressive Non-Fluent Aphasia.
APOE ?2 is associated with increased tau pathology in primary tauopathy.
Argyrophilic grain disease is a sporadic 4-repeat tauopathy.
Argyrophilic grain disease: a late-onset dementia with distinctive features among tauopathies.
Central hypoventilation in progressive supranuclear palsy.
Chameleons and mimics: Progressive supranuclear palsy and corticobasal degeneration.
Characteristics of progressive supranuclear palsy presenting with corticobasal syndrome: a cortical variant.
Contribution of the astrocytic tau pathology to synapse loss in progressive supranuclear palsy and corticobasal degeneration.
DCTN1 variation in pathologically-confirmed PSP and CBD tauopathy.
Detection of Alzheimer Disease (AD)-Specific Tau Pathology in AD and NonAD Tauopathies by Immunohistochemistry With Novel Conformation-Selective Tau Antibodies.
Detection of Alzheimer's disease (AD) specific tau pathology with conformation-selective anti-tau monoclonal antibody in co-morbid frontotemporal lobar degeneration-tau (FTLD-tau).
Development of a grape seed polyphenolic extract with anti-oligomeric activity as a novel treatment in progressive supranuclear palsy and other tauopathies.
Diagnostic Approach to Atypical Parkinsonian Syndromes.
Distinct Lysosomal Network Protein Profiles in Parkinsonian Syndrome Cerebrospinal Fluid.
Early Stage of Progressive Supranuclear Palsy: A Neuropathological Study of 324 Consecutive Autopsy Cases.
Emerging drugs for progressive supranuclear palsy.
Factors associated with development and distribution of granular/fuzzy astrocytes in neurodegenerative diseases.
Failure in heat-shock protein expression in response to UBB+1 protein in progressive supranuclear palsy in humans.
Fibrillation and molecular characteristics are coherent with clinical and pathological features of 4-repeat tauopathy caused by MAPT variant G273R.
Frameshift proteins in autosomal dominant forms of Alzheimer disease and other tauopathies.
Frontrunner in Translation: Progressive Supranuclear Palsy.
Genetic bases of Progressive Supranuclear Palsy: the MAPT tau disease.
Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study.
Genetic pleiotropy and the shared pathological features of corticobasal degeneration and progressive supranuclear palsy: a case report and a review of the literature.
Genetics of Progressive Supranuclear Palsy.
Globular glial tauopathies (GGT) presenting with motor neuron disease or frontotemporal dementia: an emerging group of 4-repeat tauopathies.
Glucocerebrosidase mutations in primary parkinsonism.
Guadeloupean parkinsonism: a cluster of progressive supranuclear palsy-like tauopathy.
Heavy metals contaminating the environment of a progressive supranuclear palsy cluster induce tau accumulation and cell death in cultured neurons.
Human tau pathology transmits glial tau aggregates in the absence of neuronal tau.
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.
Mechanisms of Cell-to-Cell Transmission of Pathological Tau: A Review.
Mechanisms of Neurodegeneration in Various Forms of Parkinsonism-Similarities and Differences.
Microglial Activation and Inflammation as a Factor in the Pathogenesis of Progressive Supranuclear Palsy (PSP).
Microtubule defects in mesenchymal stromal cells distinguish patients with Progressive Supranuclear Palsy.
Mutations in bassoon in individuals with familial and sporadic progressive supranuclear palsy-like syndrome.
Neuroligin-1 in brain and CSF of neurodegenerative disorders: investigation for synaptic biomarkers.
Parkinsonian Syndrome with Frontal Lobe Involvement and Anti-Glycine Receptor Antibodies.
Pathologic changes of progressive supranuclear palsy, corticobasal degeneration, and multiple system atrophy : Prototype and clinicopathological diversity.
Pathological and Clinical Spectrum of Progressive Supranuclear Palsy: With Special Reference to Astrocytic Tau Pathology.
Pathological correlations of [F-18]-AV-1451 imaging in non-alzheimer tauopathies.
PBB3 imaging in Parkinsonian disorders: Evidence for binding to tau and other proteins.
PERK activation mitigates tau pathology in vitro and in vivo.
PET Tau Imaging and Motor Impairments Differ Between Corticobasal Syndrome and Progressive Supranuclear Palsy With and Without Alzheimer's Disease Biomarkers.
Phosphorylated TDP-43 pathology and hippocampal sclerosis in progressive supranuclear palsy.
Post mortem cerebrospinal fluid ?-synuclein levels are raised in multiple system atrophy and distinguish this from the other ?-synucleinopathies, Parkinson's disease and Dementia with Lewy bodies.
Primary Tau Pathology, Not Copathology, Correlates With Clinical Symptoms in PSP and CBD.
Progressive Supranuclear Palsy and Corticobasal Degeneration: Pathophysiology and Treatment Options.
Progressive Supranuclear Palsy in a family with TDP-43 pathology.
Progressive supranuclear palsy, multiple system atrophy and corticobasal degeneration.
Progressive supranuclear palsy--parkinsonian disorder with tau pathology.
Protein Phosphatase 2A and Its Methylation Modulating Enzymes LCMT-1 and PME-1 Are Dysregulated in Tauopathies of Progressive Supranuclear Palsy and Alzheimer Disease.
Quantitative proteomics identifies surfactant-resistant alpha-synuclein in cerebral cortex of parkinsonism-dementia complex of Guam but not alzheimer's disease or progressive supranuclear palsy.
Radiological biomarkers for diagnosis in PSP: Where are we and where do we need to be?
Selective Vulnerability of Brainstem Nuclei in Distinct Tauopathies: A Postmortem Study.
Severity dependent distribution of impairments in PSP and CBS: Interactive visualizations.
Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia.
Sleep Disorders in Atypical Parkinsonism.
Staging disease severity in movement disorder tauopathies: brain atrophy separates progressive supranuclear palsy from corticobasal degeneration.
Tau depletion prevents progressive blood-brain barrier damage in a mouse model of tauopathy.
Tau Interacting Proteins: Gaining Insight into the Roles of Tau in Health and Disease.
Tauopathy with Hippocampal 4-Repeat Tau Immunoreactive Spherical Inclusions in a Patient with PSP.
The diagnosis of progressive supranuclear palsy: current opinions and challenges.
The Differential Diagnosis and Treatment of Atypical Parkinsonism.
The disturbance of gaze in progressive supranuclear palsy: implications for pathogenesis.
The MAPT gene is differentially methylated in the progressive supranuclear palsy brain.
The Role of Stress as a Risk Factor for Progressive Supranuclear Palsy.
Traumatic Brain Injury and Firearm Use and Risk of Progressive Supranuclear Palsy Among Veterans.
Unexpected abundance of pathological tau in progressive supranuclear palsy white matter.
Variation in tau isoform expression in different brain regions and disease states.
[18F]-T807 tauopathy PET imaging in chronic traumatic encephalopathy.
[Amyotrophic lateral sclerosis-parkinsonism-dementia complex of the Kii Peninsula of Japan]
[Progressive supranuclear palsy-Richardson syndrome with visual attention disturbance (Holmes and Horrax) and ataxie optique (Garcin): a case report].
[Progressive supranuclear palsy: what's new?].
Tetanus
Blockade of NMDA receptors unmasks a long-term depression in synaptic efficacy in rat prefrontal neurons in vitro.
Short-term synaptic plasticity contributes to the temporal filtering of electrosensory information.
Tetralogy of Fallot
Three-step preoperative sequential planning for pulmonary valve replacement in repaired tetralogy of Fallot using computed tomography.
Thiamine Deficiency
Progressive supranuclear palsy responding to intravenous thiamine: superimposed Wernicke's encephalopathy?
Thrombocytopenia
[Thrombopenia caused by pentosan polysulfate]
Thrombosis
Impact of PSP Technique on Clinical Outcomes Following Bioresorbable Scaffolds Implantation.
Poor Subpleural Perfusion Predicts Failure After Balloon Pulmonary Angioplasty for Nonoperable Chronic Thromboembolic Pulmonary Hypertension.
The rat ear vein model for investigating in vivo thrombogenicity of ultrafine particles (UFP).
Undiscovered pathology of transient scaffolding t1remains a driver of failures in clinical trials.
Tic Disorders
Premonitory urges are associated with decreased grey matter thickness within the insula and sensorimotor cortex in young people with Tourette syndrome.
Tics
Clinical genetics of familial progressive supranuclear palsy.
Premonitory sensory phenomena and suppressibility of tics in Tourette syndrome: developmental aspects in children and adolescents.
Premonitory urges are associated with decreased grey matter thickness within the insula and sensorimotor cortex in young people with Tourette syndrome.
Tourette Syndrome
Premonitory sensory phenomena and suppressibility of tics in Tourette syndrome: developmental aspects in children and adolescents.
Tremor
Application of the Unified Parkinson's Disease Rating Scale in progressive supranuclear palsy: factor analysis of the motor scale.
Atypical parkinsonism in Guadeloupe: a common risk factor for two closely related phenotypes?
Autopsy-proven progressive supranuclear palsy presenting as behavioral variant frontotemporal dementia.
Brain regional iron contents in progressive supranuclear palsy.
Clinical features and disability milestones in multiple system atrophy and progressive supranuclear palsy.
Clinical genetics of familial progressive supranuclear palsy.
Diagnostic accuracy of progressive supranuclear palsy in the Society for Progressive Supranuclear Palsy brain bank.
Effects of cerebellar neuromodulation in movement disorders: A systematic review.
Familial aggregation of parkinsonism in progressive supranuclear palsy.
Lewy body-related alpha-synucleinopathy in the aged human brain.
Predominant cortical dysfunction in Guadeloupean parkinsonism.
Speech disorders reflect differing pathophysiology in Parkinson's disease, progressive supranuclear palsy and multiple system atrophy.
The evolution of parkinsonism in primary progressive apraxia of speech: A 6-year longitudinal study.
Tremor and longevity in relatives of patients with Parkinson's disease, essential tremor, and control subjects.
Tremor in progressive supranuclear palsy.
[A 65-year-old man with Parkinsonism, gaze palsy, and dementia]
[Progressive supranuclear palsy]
Tuberculosis
Bilateral primary spontaneous pneumothorax with multiple bleb performed by VATS and wedge resection: A rare case in Indonesian adult and review article.
Biochemical characterization of phosphoserine phosphatase SerB2 from Mycobacterium marinum.
Characterization of M. tuberculosis SerB2, an essential HAD-family phosphatase, reveals novel properties.
Global discovery the PstP interactions using Mtb proteome microarray and revealing novel connections with EthR.
High Throughput Screen Identifies Small Molecule Inhibitors Specific for Mycobacterium tuberculosis Phosphoserine Phosphatase.
Identification and Repurposing of Trisubstituted Harmine Derivatives as Novel Inhibitors of Mycobacterium tuberculosis Phosphoserine Phosphatase.
Regulatory Mechanism of Mycobacterium tuberculosis Phosphoserine Phosphatase SerB2.
Rv2744c is a PspA ortholog that regulates lipid droplet homeostasis and non-replicating persistence in Mycobacterium tuberculosis.
Serine/Threonine Protein Phosphatase PstP of Mycobacterium tuberculosis Is Necessary for Accurate Cell Division and Survival of Pathogen.
The Psp system of Mycobacterium tuberculosis integrates envelope stress-sensing and envelope-preserving functions.
Tuberculosis, Pulmonary
Aetiology and clinical profile of spontaneous pneumothorax in adults.
Urinary Incontinence
Nocturnal manifestations of atypical and vascular parkinsonism: How do they differ from Parkinson's disease?
Uterine Cervical Neoplasms
A novel design for estimating relative accuracy of screening tests when complete disease verification is not feasible.
[Evaluation of PSP excretion test in diagnosis of the upper urinary tract disturbances in cases of postoperative cervical cancer]
Uveitis
Patient Support Program Increased Medication Adherence with Lower Total Health Care Costs Despite Increased Drug Spending.
Vascular Diseases
A clinicopathological study of vascular progressive supranuclear palsy: a multi-infarct disorder presenting as progressive supranuclear palsy.
The neuropathology of progressive supranuclear palsy.
Vascular progressive supranuclear palsy.
Vascular System Injuries
Vascular Parkinsonism: deconstructing a syndrome.
Vasculitis
Poststeroid panniculitis.
Virus Diseases
Pinon shell polysaccharide enhances immunity against H9N2 avian influenza virus in chickens.
Respiratory virus associated with surgery in children patients.
Serine/threonine protein phosphatase is required for tobacco mosaic virus-mediated programmed cell death.
Wernicke Encephalopathy
Progressive supranuclear palsy responding to intravenous thiamine: superimposed Wernicke's encephalopathy?
Williams Syndrome
Phosphoserine phosphatase deficiency in a patient with Williams syndrome.
Xerostomia
A meta-analysis of the pros and cons of partial superficial parotidectomy versus superficial parotidectomy for the treatment of benign parotid neoplasms.