EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   3.1.6.12 | arylsulfatase (type i) deficiency |
2903054 |
Multiple sulfatase deficiency with a novel biochemical presentation. |
causal interaction
diagnostic usage
unassigned |
3
2
0 |
| 3.1.6.12 | Carcinoma, Hepatocellular |
1968043 |
Human arylsulfatase B: MOPAC cloning, nucleotide sequence of a full-length cDNA, and regions of amino acid identity with arylsulfatases A and C. |
ongoing research
unassigned |
3
0 |
| 3.1.6.12 | Dentigerous Cyst |
6435047 |
Occurrence of multiple dentigerous cysts in a patient with the Maroteaux-Lamy syndrome (mucopolysaccharidosis, type VI). |
causal interaction
unassigned |
4
0 |
| 3.1.6.12 | Dysostoses |
9356736 |
Effect of enzyme replacement therapy on bone formation in a feline model of mucopolysaccharidosis type VI. |
causal interaction
unassigned |
4
0 |
| 3.1.6.12 | Hypersensitivity |
9685627 |
Immune response to enzyme replacement therapy: clinical signs of hypersensitivity reactions and altered enzyme distribution in a high titre rat model. |
ongoing research
unassigned |
2
0 |
| 3.1.6.12 | Leukodystrophy, Metachromatic |
2903054 |
Multiple sulfatase deficiency with a novel biochemical presentation. |
causal interaction
diagnostic usage
unassigned |
3
2
0 |
| 3.1.6.12 | Lysosomal Storage Diseases |
9421472 |
Two mutations within a feline mucopolysaccharidosis type VI colony cause three different clinical phenotypes. |
causal interaction
unassigned |
4
0 |
| 3.1.6.12 | Lysosomal Storage Diseases |
11802522 |
Mucopolysaccharidosis type VI: Report of two Taiwanese patients and identification of one novel mutation. |
causal interaction
unassigned |
4
0 |
| 3.1.6.12 | Lysosomal Storage Diseases |
15895715 |
Pharmacokinetic profile of recombinant human N-acetylgalactosamine 4-sulphatase enzyme replacement therapy in patients with mucopolysaccharidosis VI (Maroteaux-Lamy syndrome): a phase I/II study. |
causal interaction
ongoing research
therapeutic application
unassigned |
3
4
3
0 |
| 3.1.6.12 | Lysosomal Storage Diseases |
15930196 |
Direct comparison of measures of endurance, mobility, and joint function during enzyme-replacement therapy of mucopolysaccharidosis VI (Maroteaux-Lamy syndrome): results after 48 weeks in a phase 2 open-label clinical study of recombinant human N-acetylgalactosamine 4-sulfatase. |
causal interaction
ongoing research
therapeutic application
unassigned |
3
3
4
0 |
