EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
3.1.6.8 | Adrenoleukodystrophy |
10560915 |
Bone marrow-derived mesenchymal stem cells remain host-derived despite successful hematopoietic engraftment after allogeneic transplantation in patients with lysosomal and peroxisomal storage diseases. |
diagnostic usage ongoing research therapeutic application unassigned |
3 2 1 0 |
3.1.6.8 | arylsulfatase (type i) deficiency |
2903054 |
Multiple sulfatase deficiency with a novel biochemical presentation. |
causal interaction diagnostic usage unassigned |
3 2 0 |
3.1.6.8 | arylsulfatase (type i) deficiency |
6108718 |
Retinal pigment epithelial degeneration associated with leukocytic arylsulfatase A deficiency. |
diagnostic usage unassigned |
3 0 |
3.1.6.8 | Breast Diseases |
11295292 |
Evaluation of leukocyte arylsulfatase-A activity in patients with breast cancer and benign breast disease. |
diagnostic usage ongoing research unassigned |
4 3 0 |
3.1.6.8 | Breast Neoplasms |
11295292 |
Evaluation of leukocyte arylsulfatase-A activity in patients with breast cancer and benign breast disease. |
diagnostic usage ongoing research unassigned |
4 3 0 |
3.1.6.8 | Cerebral Palsy |
16613739 |
Kinetics and activity of arylsulfatase A in leukocytes derived from patients with cerebral palsy. |
causal interaction diagnostic usage ongoing research unassigned |
4 1 3 0 |
3.1.6.8 | cerebroside-sulfatase deficiency |
1968615 |
Deficient glycosylation of arylsulfatase A in pseudo arylsulfatase-A deficiency. |
causal interaction therapeutic application unassigned |
4 1 0 |
3.1.6.8 | cerebroside-sulfatase deficiency |
5257010 |
Metachromatic leukodystrophy: arylsulfatase-A deficiency in skin fibroblast cultures. |
unassigned |
0 |
3.1.6.8 | cerebroside-sulfatase deficiency |
6580647 |
Pseudo arylsulfatase-A deficiency in healthy individuals: genetic and biochemical relationship to metachromatic leukodystrophy. |
causal interaction diagnostic usage unassigned |
4 3 0 |
3.1.6.8 | cerebroside-sulfatase deficiency |
8456837 |
Complications in the genotypic molecular diagnosis of pseudo arylsulfatase A deficiency. |
causal interaction diagnostic usage therapeutic application unassigned |
4 4 1 0 |