1-anilino-8-naphthalenesulfonate has been researched along with Glycogen Storage Disease in 3 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.
Glycogen Storage Disease: A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent liver involvement is presented. In others, more generalized storage of glycogen occurs, sometimes with prominent cardiac involvement.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 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 |
|---|---|
| Asayama, K | 1 |
| Kato, K | 1 |
| Anemiya, S | 1 |
| Nozaki, Y | 1 |
| Galton, DJ | 1 |
| Betteridge, DJ | 1 |
| Taylor, KG | 1 |
| Holdsworth, G | 1 |
| Stocks, J | 1 |
| Gamlen, TR | 1 |
| Muller, DP | 1 |
| Wolff, OH | 1 |
3 other studies available for 1-anilino-8-naphthalenesulfonate and Glycogen Storage Disease
| Article | Year |
|---|---|
Postheparin plasma lipases in patients with hepatic glycogenosis.
Topics: Adolescent; Child; Child, Preschool; Female; Glycogen Storage Disease; Heparin; Humans; Infant; Lipa | 1982 |
Defects of enzyme regulation in metabolic disease.
Topics: Allosteric Regulation; Glycogen Storage Disease; Gout; Humans; Hydroxymethylglutaryl CoA Reductases; | 1977 |
Lipoprotein lipase and hepatic lipase activities in children with hyperlipidaemia.
Topics: Adipose Tissue; Adult; Animals; Child; Glycogen Storage Disease; Humans; Hyperlipidemias; Hyperlipop | 1979 |