Disease on EC 1.8.3.1 - sulfite oxidase
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arylsulfatase (type i) deficiency
Antenatal manifestations of inborn errors of metabolism: autopsy findings suggestive of a metabolic disorder.
aspartate-ammonia ligase deficiency
Antenatal manifestations of inborn errors of metabolism: autopsy findings suggestive of a metabolic disorder.
Asthma
A simulated patient study to evaluate community pharmacist assessment, management and advice giving to patients with asthma.
Brain Diseases
Bezafibrate prevents mitochondrial dysfunction, antioxidant system disturbance, glial reactivity and neuronal damage induced by sulfite administration in striatum of rats: Implications for a possible therapeutic strategy for sulfite oxidase deficiency.
Brain Diseases
Prenatal multicystic encephalopathy in isolated sulfite oxidase deficiency with a novel mutaion.
Carcinoma, Hepatocellular
SUOX is a promising diagnostic and prognostic biomarker for hepatocellular carcinoma.
Cardiovascular Diseases
Nutrition education in supermarkets: an unsuccessful attempt to influence knowledge and product sales.
Congenital Disorders of Glycosylation
Antenatal manifestations of inborn errors of metabolism: autopsy findings suggestive of a metabolic disorder.
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Antenatal manifestations of inborn errors of metabolism: autopsy findings suggestive of a metabolic disorder.
Conjunctivitis, Allergic
The management of ocular allergy in community pharmacies in the United Kingdom.
Craniocerebral Trauma
Metabolic crisis after trivial head trauma in late-onset isolated sulfite oxidase deficiency: Report of two new cases and review of published patients.
Cystic Fibrosis
Strong anion determination in biological fluids by capillary electrophoresis for clinical diagnostics.
Dystonia
A review of the clinical presentation and laboratory findings in two uncommon hereditary disorders of sulfur amino acid metabolism, beta-mercaptolactate cysteine disulfideuria and sulfite oxidase deficiency.
Encephalomalacia
Functional deficiencies of sulfite oxidase: Differential diagnoses in neonates presenting with intractable seizures and cystic encephalomalacia.
Encephalomalacia
Isolated sulfite oxidase deficiency: a case report with a novel mutation and review of the literature.
Encephalomalacia
Proton Magnetic Resonance Spectroscopy And Diffusion-weighted Imaging In Isolated Sulfite Oxidase Deficiency.
Epilepsy
Infantile spasms and hyperekplexia associated with isolated sulfite oxidase deficiency.
Genetic Diseases, Inborn
The role of glutamate oxaloacetate transaminases in sulfite biosynthesis and H2S metabolism.
Glycogen Storage Disease
Antenatal manifestations of inborn errors of metabolism: autopsy findings suggestive of a metabolic disorder.
Homocystinuria
Absence of hepatic molybdenum cofactor. An inborn error of metabolism associated with lens dislocation.
Hyperekplexia
Infantile spasms and hyperekplexia associated with isolated sulfite oxidase deficiency.
Hyperglycinemia, Nonketotic
Antenatal manifestations of inborn errors of metabolism: autopsy findings suggestive of a metabolic disorder.
Hyperglycinemia, Nonketotic
[Prenatal symptoms and diagnosis of inherited metabolic diseases].
Hypophosphatasia
Antenatal manifestations of inborn errors of metabolism: autopsy findings suggestive of a metabolic disorder.
Hypoxia-Ischemia, Brain
??mTc-ethyl cysteinate dimer cranial single-photon emission computed tomography and serial cranial magnetic resonance imaging in a girl with isolated sulfite oxidase deficiency.
Hypoxia-Ischemia, Brain
Clinical and imaging observations in isolated sulfite oxidase deficiency.
Hypoxia-Ischemia, Brain
Teaching NeuroImages: Early imaging of sulfite oxidase deficiency mimics severe hypoxic ischemic encephalopathy.
Hypoxia-Ischemia, Brain
Very early neuroimages of sulfite oxidase deficiency mimicing severe hypoxic ischemic encephalopathy in a neonate.
Infections
Availability of Sexually Transmitted Infection Screening and Expedited Partner Therapy at Federally Qualified Health Centers in Michigan.
Infections
Shopper cards data and storage practices for the investigation of an outbreak of Shiga-toxin producing Escherichia coli O157 infections.
Intellectual Disability
DNA-based diagnosis of isolated sulfite oxidase deficiency by denaturing high-performance liquid chromatography.
Intellectual Disability
Infantile spasms and hyperekplexia associated with isolated sulfite oxidase deficiency.
Intellectual Disability
Molybdenum cofactor deficiency: Identification of a patient with homozygote mutation in the MOCS3 gene.
Leukodystrophy, Globoid Cell
Clinical and neuroimaging features as diagnostic guides in neonatal neurology diseases with cerebellar involvement.
Leukoencephalopathies
Isolated sulfite oxidase deficiency in the newborn: lactic acidaemia and leukoencephalopathy.
Lysosomal Storage Diseases
Antenatal manifestations of inborn errors of metabolism: autopsy findings suggestive of a metabolic disorder.
Metabolic Diseases
Machine learning-based identification and characterization of 15 novel pathogenic SUOX missense mutations.
Metabolism, Inborn Errors
Functional deficiencies of sulfite oxidase: Differential diagnoses in neonates presenting with intractable seizures and cystic encephalomalacia.
Metabolism, Inborn Errors
Prenatal diagnosis of molybdenum cofactor deficiency and isolated sulfite oxidase deficiency.
Muscle Hypotonia
Magnetic resonance imaging and magnetic resonance spectroscopy in isolated sulfite oxidase deficiency.
Neoplasms
Accessibility and Barriers to Oncology Appointments at 40 National Cancer Institute-Designated Comprehensive Cancer Centers: Results of a Mystery Shopper Project.
Neoplasms
High sulfite oxidase expression could predict postoperative biochemical recurrence in patients with prostate cancer.
Nervous System Diseases
Isolated sulfite oxidase deficiency: mutation analysis and DNA-based prenatal diagnosis.
Nervous System Diseases
The peak height ratio of S-sulfonated transthyretin and other oxidized isoforms as a marker for molybdenum cofactor deficiency, measured by electrospray ionization mass spectrometry.
Neurologic Manifestations
Sulfite oxidase deficiency: clinical, neuroradiologic, and biochemical features in two new patients.
Peroxisomal Disorders
Antenatal manifestations of inborn errors of metabolism: autopsy findings suggestive of a metabolic disorder.
persulfide dioxygenase deficiency
Evidence that Thiosulfate Inhibits Creatine Kinase Activity in Rat Striatum via Thiol Group Oxidation.
Prostatic Neoplasms
High sulfite oxidase expression could predict postoperative biochemical recurrence in patients with prostate cancer.
Psychomotor Disorders
Development of a rapid UPLC-MS/MS determination of urine sulfocysteine for diagnosis of sulfocysteinuria and molybdenum co-factor deficiencies.
pyruvate carboxylase deficiency
Antenatal manifestations of inborn errors of metabolism: autopsy findings suggestive of a metabolic disorder.
Pyruvate Carboxylase Deficiency Disease
Antenatal manifestations of inborn errors of metabolism: autopsy findings suggestive of a metabolic disorder.
pyruvate dehydrogenase (nadp+) deficiency
Antenatal manifestations of inborn errors of metabolism: autopsy findings suggestive of a metabolic disorder.
Pyruvate Dehydrogenase Complex Deficiency Disease
Antenatal manifestations of inborn errors of metabolism: autopsy findings suggestive of a metabolic disorder.
Respiratory Insufficiency
2-Mercaptoethanesulfonate-cysteine disulfide excretion following the administration of 2-mercaptoethanesulfonate--a pitfall in the diagnosis of sulfite oxidase deficiency.
Seizures
2-Mercaptoethanesulfonate-cysteine disulfide excretion following the administration of 2-mercaptoethanesulfonate--a pitfall in the diagnosis of sulfite oxidase deficiency.
Seizures
Bezafibrate prevents mitochondrial dysfunction, antioxidant system disturbance, glial reactivity and neuronal damage induced by sulfite administration in striatum of rats: Implications for a possible therapeutic strategy for sulfite oxidase deficiency.
Seizures
Development of a rapid UPLC-MS/MS determination of urine sulfocysteine for diagnosis of sulfocysteinuria and molybdenum co-factor deficiencies.
Seizures
DNA-based diagnosis of isolated sulfite oxidase deficiency by denaturing high-performance liquid chromatography.
Seizures
Functional deficiencies of sulfite oxidase: Differential diagnoses in neonates presenting with intractable seizures and cystic encephalomalacia.
Seizures
Higher susceptibility of cerebral cortex and striatum to sulfite neurotoxicity in sulfite oxidase-deficient rats.
Seizures
Isolated sulfite oxidase deficiency: a case report with a novel mutation and review of the literature.
Seizures
Isolated sulfite oxidase deficiency: mutation analysis and DNA-based prenatal diagnosis.
Seizures
Magnetic resonance imaging and magnetic resonance spectroscopy in isolated sulfite oxidase deficiency.
Seizures
Pyridoxine-dependent epilepsy with elevated urinary ?-amino adipic semialdehyde in molybdenum cofactor deficiency.
Seizures
The sulfite oxidase Shopper controls neuronal activity by regulating glutamate homeostasis in Drosophila ensheathing glia.
Sexually Transmitted Diseases
Availability of Sexually Transmitted Infection Screening and Expedited Partner Therapy at Federally Qualified Health Centers in Michigan.
Spasms, Infantile
Infantile spasms and hyperekplexia associated with isolated sulfite oxidase deficiency.
Stomach Neoplasms
Sulfite Oxidase Is a Novel Prognostic Biomarker of Advanced Gastric Cancer.
sulfite oxidase deficiency
2-Mercaptoethanesulfonate-cysteine disulfide excretion following the administration of 2-mercaptoethanesulfonate--a pitfall in the diagnosis of sulfite oxidase deficiency.
sulfite oxidase deficiency
??mTc-ethyl cysteinate dimer cranial single-photon emission computed tomography and serial cranial magnetic resonance imaging in a girl with isolated sulfite oxidase deficiency.
sulfite oxidase deficiency
A compound heterozygote case of isolated sulfite oxidase deficiency.
sulfite oxidase deficiency
A mechanism of sulfite neurotoxicity: direct inhibition of glutamate dehydrogenase.
sulfite oxidase deficiency
A review of the clinical presentation and laboratory findings in two uncommon hereditary disorders of sulfur amino acid metabolism, beta-mercaptolactate cysteine disulfideuria and sulfite oxidase deficiency.
sulfite oxidase deficiency
A simple screening test for sulfite oxidase deficiency: detection of urinary thiosulfate by a modification of Sörbo's method.
sulfite oxidase deficiency
Absence of hepatic molybdenum cofactor. An inborn error of metabolism associated with lens dislocation.
sulfite oxidase deficiency
Ampicillin interference with test for sulfite oxidase deficiency.
sulfite oxidase deficiency
An inborn error of metabolism presenting as hypoxic-ischemic insult.
sulfite oxidase deficiency
Bezafibrate prevents mitochondrial dysfunction, antioxidant system disturbance, glial reactivity and neuronal damage induced by sulfite administration in striatum of rats: Implications for a possible therapeutic strategy for sulfite oxidase deficiency.
sulfite oxidase deficiency
Biological applications of a turn-on bioluminescent probe for monitoring sulfite oxidase deficiency in vivo.
sulfite oxidase deficiency
Ceruloplasmin, copper, selenium, iron, zinc, and manganese levels in normal and sulfite oxidase deficient rat plasma: effects of sulfite exposure.
sulfite oxidase deficiency
Clinical and imaging observations in isolated sulfite oxidase deficiency.
sulfite oxidase deficiency
Clinical and neuroimaging features as diagnostic guides in neonatal neurology diseases with cerebellar involvement.
sulfite oxidase deficiency
Cysteine-S-sulfate: brain damaging metabolite in sulfite oxidase deficiency.
sulfite oxidase deficiency
Development of a rapid UPLC-MS/MS determination of urine sulfocysteine for diagnosis of sulfocysteinuria and molybdenum co-factor deficiencies.
sulfite oxidase deficiency
Distribution, metabolism and toxicity of inhaled sulfur dioxide and endogenously generated sulfite in the respiratory tract of normal and sulfite oxidase-deficient rats.
sulfite oxidase deficiency
Disturbance of brain energy and redox homeostasis provoked by sulfite and thiosulfate: Potential pathomechanisms involved in the neuropathology of sulfite oxidase deficiency.
sulfite oxidase deficiency
DNA-based diagnosis of isolated sulfite oxidase deficiency by denaturing high-performance liquid chromatography.
sulfite oxidase deficiency
Elucidating the catalytic mechanism of sulfite oxidizing enzymes using structural, spectroscopic, and kinetic analyses.
sulfite oxidase deficiency
Functional deficiencies of sulfite oxidase: Differential diagnoses in neonates presenting with intractable seizures and cystic encephalomalacia.
sulfite oxidase deficiency
Health effects of atmospheric sulfur dioxide and dietary sulfites. The fallacy of typology.
sulfite oxidase deficiency
Human sulfite oxidase deficiency. Characterization of the molecular defect in a multicomponent system.
sulfite oxidase deficiency
Human sulfite oxidase R160Q: identification of the mutation in a sulfite oxidase-deficient patient and expression and characterization of the mutant enzyme.
sulfite oxidase deficiency
Identification of a novel SUOX pathogenic variants as the cause of isolated sulfite oxidase deficiency in a Chinese pedigree.
sulfite oxidase deficiency
Impaired mitochondrial maturation of sulfite oxidase in a patient with severe sulfite oxidase deficiency.
sulfite oxidase deficiency
Infantile spasms and hyperekplexia associated with isolated sulfite oxidase deficiency.
sulfite oxidase deficiency
Isolated sulfite oxidase deficiency in the newborn: lactic acidaemia and leukoencephalopathy.
sulfite oxidase deficiency
Isolated sulfite oxidase deficiency: a case report with a novel mutation and review of the literature.
sulfite oxidase deficiency
Isolated sulfite oxidase deficiency: identification of 12 novel SUOX mutations in 10 patients.
sulfite oxidase deficiency
Isolated sulfite oxidase deficiency: mutation analysis and DNA-based prenatal diagnosis.
sulfite oxidase deficiency
Isolated sulfite oxidase deficiency: review of two cases in one family.
sulfite oxidase deficiency
Kinetic results for mutations of conserved residues H304 and R309 of human sulfite oxidase point to mechanistic complexities.
sulfite oxidase deficiency
Machine learning-based identification and characterization of 15 novel pathogenic SUOX missense mutations.
sulfite oxidase deficiency
Magnetic resonance imaging and magnetic resonance spectroscopy in isolated sulfite oxidase deficiency.
sulfite oxidase deficiency
Metabolic crisis after trivial head trauma in late-onset isolated sulfite oxidase deficiency: Report of two new cases and review of published patients.
sulfite oxidase deficiency
Metabolic stroke in a late-onset form of isolated sulfite oxidase deficiency.
sulfite oxidase deficiency
Microarray analysis unmasked paternal uniparental disomy of chromosome 12 in a patient with isolated sulfite oxidase deficiency.
sulfite oxidase deficiency
Molecular basis of sulfite oxidase deficiency from the structure of sulfite oxidase.
sulfite oxidase deficiency
Molybdenum cofactor and isolated sulphite oxidase deficiencies: Clinical and molecular spectrum among Egyptian patients.
sulfite oxidase deficiency
Molybdenum cofactor deficiency in a patient previously characterized as deficient in sulfite oxidase.
sulfite oxidase deficiency
Molybdenum cofactor deficiency: a new HPLC method for fast quantification of s-sulfocysteine in urine and serum.
sulfite oxidase deficiency
Molybdenum Cofactor Deficiency: Mega Cisterna Magna in Two Consecutive Pregnancies and Review of the Literature.
sulfite oxidase deficiency
Molybdenum cofactor deficiency: metabolic link between taurine and s-sulfocysteine.
sulfite oxidase deficiency
Molybdenum cofactor deficiency: Mutations in GPHN, MOCS1 and MOCS2.
sulfite oxidase deficiency
Molybdenum Trioxide Nanoparticles with Intrinsic Sulfite Oxidase Activity.
sulfite oxidase deficiency
Novel Compound Heterozygous Pathogenic Variants in SUOX Cause Isolated Sulfite Oxidase Deficiency in a Chinese Han Family.
sulfite oxidase deficiency
Ophthalmic abnormalities in molybdenum cofactor deficiency and isolated sulfite oxidase deficiency.
sulfite oxidase deficiency
Oxygen reactivity of mammalian sulfite oxidase provides a concept for the treatment of sulfite oxidase deficiency.
sulfite oxidase deficiency
Postmortem whole-genome sequencing on a dried blood spot identifies a novel homozygous SUOX variant causing isolated sulfite oxidase deficiency.
sulfite oxidase deficiency
Preimplantation genetic diagnosis in isolated sulfite oxidase deficiency.
sulfite oxidase deficiency
Prenatal brain disruption in isolated sulfite oxidase deficiency.
sulfite oxidase deficiency
Prenatal diagnosis of molybdenum cofactor deficiency and isolated sulfite oxidase deficiency.
sulfite oxidase deficiency
Prenatal multicystic encephalopathy in isolated sulfite oxidase deficiency with a novel mutaion.
sulfite oxidase deficiency
Proton Magnetic Resonance Spectroscopy And Diffusion-weighted Imaging In Isolated Sulfite Oxidase Deficiency.
sulfite oxidase deficiency
Pyridoxine-dependent epilepsy with elevated urinary ?-amino adipic semialdehyde in molybdenum cofactor deficiency.
sulfite oxidase deficiency
Screening for sulfite oxidase deficiency with urinary thiosulfate/sulfate ratios determined by anion chromatography.
sulfite oxidase deficiency
Severe isolated sulfide oxidase deficiency with a novel mutation.
sulfite oxidase deficiency
Simultaneous occurrence of xanthine oxidase and sulfite oxidase deficiency. A molybdenum dependent inborn error of metabolism?
sulfite oxidase deficiency
Stable clinical course in three siblings with late-onset isolated sulfite oxidase deficiency: a case series and literature review.
sulfite oxidase deficiency
Strong anion determination in biological fluids by capillary electrophoresis for clinical diagnostics.
sulfite oxidase deficiency
Structural analysis of missense mutations causing isolated sulfite oxidase deficiency.
sulfite oxidase deficiency
Structures and reaction pathways of the molybdenum centres of sulfite-oxidizing enzymes by pulsed EPR spectroscopy.
sulfite oxidase deficiency
Sulfite increases lipoperoxidation and decreases the activity of catalase in brain of rats.
sulfite oxidase deficiency
Sulfite leads to neuron loss in the hippocampus of both normal and SOX-deficient rats.
sulfite oxidase deficiency
Sulfite Oxidase Activity of Cytochrome c: Role of Hydrogen Peroxide.
sulfite oxidase deficiency
Sulfite oxidase deficiency - An unusual late and mild presentation.
sulfite oxidase deficiency
Sulfite oxidase deficiency in man: demonstration of the enzymatic defect.
sulfite oxidase deficiency
Sulfite oxidase deficiency. Biochemical and clinical investigations of a hereditary metabolic disorder in sulfur metabolism.
sulfite oxidase deficiency
Sulfite oxidase deficiency: a high risk factor in SO2, sulfite, and bisulfite toxicity?
sulfite oxidase deficiency
Sulfite oxidase deficiency: clinical, neuroradiologic, and biochemical features in two new patients.
sulfite oxidase deficiency
Teaching NeuroImages: Early imaging of sulfite oxidase deficiency mimics severe hypoxic ischemic encephalopathy.
sulfite oxidase deficiency
The central active site arginine in sulfite oxidizing enzymes alters kinetic properties by controlling electron transfer and redox interactions.
sulfite oxidase deficiency
The effect of inhaled sulfur dioxide and systemic sulfite on the induction of lung carcinoma in rats by benzo[a]pyrene.
sulfite oxidase deficiency
The G473D Mutation Impairs Dimerization and Catalysis in Human Sulfite Oxidase.
sulfite oxidase deficiency
The role of glutamate oxaloacetate transaminases in sulfite biosynthesis and H2S metabolism.
sulfite oxidase deficiency
The Role of Oxidative Stress and Bioenergetic Dysfunction in Sulfite Oxidase Deficiency: Insights from Animal Models.
sulfite oxidase deficiency
Total truncation of the molybdopterin/dimerization domains of SUOX protein in an Arab family with isolated sulfite oxidase deficiency.
sulfite oxidase deficiency
Very early neuroimages of sulfite oxidase deficiency mimicing severe hypoxic ischemic encephalopathy in a neonate.
sulfite oxidase deficiency
Visual evoked potentials in normal and sulfite oxidase deficient rats exposed to ingested sulfite.
sulfite oxidase deficiency
[Prenatal symptoms and diagnosis of inherited metabolic diseases].
sulfite oxidase deficiency
[Sulfite oxidase activity deficiency caused by cofactor molybdenum deficiency: A case of early severe encephalopathy].
transaldolase deficiency
Antenatal manifestations of inborn errors of metabolism: autopsy findings suggestive of a metabolic disorder.
Urolithiasis
Strong anion determination in biological fluids by capillary electrophoresis for clinical diagnostics.
xanthine dehydrogenase deficiency
Biochemical investigation of a child with molybdenum cofactor deficiency.
xanthine oxidase deficiency
Successful treatment of molybdenum cofactor deficiency type A with cPMP.
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