1-anilino-8-naphthalenesulfonate has been researched along with Mucopolysaccharidosis I in 2 studies
1-anilino-8-naphthalenesulfonate: RN given refers to parent cpd
8-anilinonaphthalene-1-sulfonic acid : A naphthalenesulfonic acid that is naphthalene-1-sulfonic acid substituted by a phenylamino group at position 8.
Mucopolysaccharidosis I: Systemic lysosomal storage disease caused by a deficiency of alpha-L-iduronidase (IDURONIDASE) and characterized by progressive physical deterioration with urinary excretion of DERMATAN SULFATE and HEPARAN SULFATE. There are three recognized phenotypes representing a spectrum of clinical severity from severe to mild: Hurler syndrome, Hurler-Scheie syndrome and Scheie syndrome (formerly mucopolysaccharidosis V). Symptoms may include DWARFISM; hepatosplenomegaly; thick, coarse facial features with low nasal bridge; corneal clouding; cardiac complications; and noisy breathing.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (50.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Pittman, RC | 1 |
| Williams, JC | 1 |
| Miller, AL | 1 |
| Steinberg, D | 1 |
| Rabinowitz, JL | 1 |
| Sheridan, O | 1 |
| Craig, RG | 1 |
| Feldman, R | 1 |
| Grossman, ER | 1 |
| Harvey, CE | 1 |
| Haskins, ME | 1 |
2 other studies available for 1-anilino-8-naphthalenesulfonate and Mucopolysaccharidosis I
| Article | Year |
|---|---|
Acid acylhydrolase deficiency in I-cell disease and pseudo-Hurler polydystrophy.
Topics: Carboxylic Ester Hydrolases; Fibroblasts; Humans; Hydrogen-Ion Concentration; Lipase; Lipids; Liver; | 1979 |
Lipid composition and biosynthesis in the gingiva of the domestic cat.
Topics: Acetates; Animals; Carbon Radioisotopes; Cats; Disease Models, Animal; Gingiva; Gingivitis; Lipase; | 1991 |