1-anilino-8-naphthalenesulfonate has been researched along with Acid beta-Glucosidase Deficiency in 7 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.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (71.43) | 18.7374 |
| 1990's | 2 (28.57) | 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 |
|---|---|
| BRAUNSTEINER, H | 1 |
| DIENSTL, F | 1 |
| SAILER, S | 1 |
| SANDHOFER, F | 1 |
| Gatt, S | 1 |
| Barenholz, Y | 1 |
| Goldberg, R | 1 |
| Dinur, T | 1 |
| Besley, G | 1 |
| Leibovitz-Ben Gershon, Z | 1 |
| Rosenthal, J | 1 |
| Desnick, RJ | 1 |
| Devine, EA | 1 |
| Shafit-Zagardo, B | 1 |
| Tsuruki, F | 1 |
| vom Dahl, S | 1 |
| Harzer, K | 1 |
| Rolfs, A | 1 |
| Albrecht, B | 1 |
| Niederau, C | 1 |
| Vogt, C | 1 |
| van Weely, S | 1 |
| Aerts, J | 1 |
| Müller, G | 1 |
| Häussinger, D | 1 |
| Röyttä, M | 1 |
| Fagerlund, AS | 1 |
| Toikkanen, S | 1 |
| Salmi, TT | 1 |
| Jorde, LB | 1 |
| Forsius, HR | 1 |
| Eriksson, AW | 1 |
| Douste-Blazy, L | 1 |
| Nègre, A | 1 |
| Maret, A | 1 |
| Salvayre, R | 1 |
| Sloan, HR | 2 |
| Fredrickson, DS | 1 |
1 review available for 1-anilino-8-naphthalenesulfonate and Acid beta-Glucosidase Deficiency
| Article | Year |
|---|---|
Affinity chromatography of enzymes hydrolyzing sphingolipids.
Topics: Chromatography, Affinity; Diagnosis, Differential; Gaucher Disease; Humans; Hydrolases; Hydrolysis; | 1973 |
6 other studies available for 1-anilino-8-naphthalenesulfonate and Acid beta-Glucosidase Deficiency
| Article | Year |
|---|---|
[ESTERASE AND LIPASE ACTIVITY IN WHITE BLOOD CELLS].
Topics: Bone Marrow Diseases; Carbohydrate Metabolism; Cocos; Esterases; Exudates and Transudates; Fatty Aci | 1963 |
Assay of enzymes of lipid metabolism with colored and fluorescent derivatives of natural lipids.
Topics: Animals; Bile; Brain; Cells, Cultured; Galactosidases; Galactosylceramidase; Gaucher Disease; Glucos | 1981 |
Hepatosplenomegalic lipidosis: what unless Gaucher? Adult cholesteryl ester storage disease (CESD) with anemia, mesenteric lipodystrophy, increased plasma chitotriosidase activity and a homozygous lysosomal acid lipase -1 exon 8 splice junction mutation.
Topics: Adult; Anemia; Cholesterol Ester Storage Disease; Diagnosis, Differential; DNA, Recombinant; Exons; | 1999 |
Wolman disease: morphological, clinical and genetic studies on the first Scandinavian cases.
Topics: Consanguinity; Diagnostic Errors; Female; Finland; Gaucher Disease; Humans; Infant; Lipase; Male; Pe | 1992 |
[Value of studying isoenzymes in hereditary lysosomal lipidoses. In particular beta-glucosidase (Gaucher's disease) and acid lipase (Wolman's disease and cholesterol ester storage disease)].
Topics: beta-Glucosidase; Gaucher Disease; Glucosidases; Humans; Isoenzymes; Lipase; Lipidoses | 1985 |
Enzyme deficiency in cholesteryl ester storage idisease.
Topics: Adult; Aged; Aorta; Autopsy; Cholesterol; Chromatography, Thin Layer; Esterases; Esters; Gaucher Dis | 1972 |