1-anilino-8-naphthalenesulfonate has been researched along with Liver Failure 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.
Liver Failure: Severe inability of the LIVER to perform its normal metabolic functions, as evidenced by severe JAUNDICE and abnormal serum levels of AMMONIA; BILIRUBIN; ALKALINE PHOSPHATASE; ASPARTATE AMINOTRANSFERASE; LACTATE DEHYDROGENASES; and albumin/globulin ratio. (Blakiston's Gould Medical Dictionary, 4th ed)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Senkerikova, R | 1 |
| Frankova, S | 1 |
| Jirsa, M | 1 |
| Kreidlova, M | 1 |
| Merta, D | 1 |
| Neroldova, M | 1 |
| Chmelova, K | 1 |
| Spicak, J | 1 |
| Sperl, J | 1 |
| Mandorfer, M | 1 |
| Scheiner, B | 1 |
| Stättermayer, AF | 1 |
| Schwabl, P | 1 |
| Paternostro, R | 1 |
| Bauer, D | 1 |
| Schaefer, B | 1 |
| Zoller, H | 1 |
| Peck-Radosavljevic, M | 1 |
| Trauner, M | 1 |
| Reiberger, T | 1 |
| Ferenci, P | 1 |
| Ferlitsch, A | 1 |
| Fujiyama, J | 1 |
| Sakuraba, H | 1 |
| Kuriyama, M | 1 |
| Fujita, T | 1 |
| Nagata, K | 1 |
| Nakagawa, H | 1 |
| Osame, M | 1 |
3 other studies available for 1-anilino-8-naphthalenesulfonate and Liver Failure
| Article | Year |
|---|---|
PNPLA3 rs738409 G allele carriers with genotype 1b HCV cirrhosis have lower viral load but develop liver failure at younger age.
Topics: Alleles; Carcinoma, Hepatocellular; Case-Control Studies; Cross-Sectional Studies; Female; Genetic P | 2019 |
Impact of patatin-like phospholipase domain containing 3 rs738409 G/G genotype on hepatic decompensation and mortality in patients with portal hypertension.
Topics: Adult; Aged; Cross-Sectional Studies; Fatty Liver; Female; Genetic Predisposition to Disease; Genoty | 2018 |
A new mutation (LIPA Tyr22X) of lysosomal acid lipase gene in a Japanese patient with Wolman disease.
Topics: Anemia; Cells, Cultured; Consanguinity; Fatal Outcome; Female; Fibroblasts; Genotype; Humans; Infant | 1996 |