Page last updated: 2024-10-21

1-anilino-8-naphthalenesulfonate and Hepatic Failure

1-anilino-8-naphthalenesulfonate has been researched along with Hepatic 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.

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (33.33)18.2507
2000's0 (0.00)29.6817
2010's2 (66.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Senkerikova, R1
Frankova, S1
Jirsa, M1
Kreidlova, M1
Merta, D1
Neroldova, M1
Chmelova, K1
Spicak, J1
Sperl, J1
Mandorfer, M1
Scheiner, B1
Stättermayer, AF1
Schwabl, P1
Paternostro, R1
Bauer, D1
Schaefer, B1
Zoller, H1
Peck-Radosavljevic, M1
Trauner, M1
Reiberger, T1
Ferenci, P1
Ferlitsch, A1
Fujiyama, J1
Sakuraba, H1
Kuriyama, M1
Fujita, T1
Nagata, K1
Nakagawa, H1
Osame, M1

Other Studies

3 other studies available for 1-anilino-8-naphthalenesulfonate and Hepatic Failure

ArticleYear
PNPLA3 rs738409 G allele carriers with genotype 1b HCV cirrhosis have lower viral load but develop liver failure at younger age.
    PloS one, 2019, Volume: 14, Issue:9

    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.
    Alimentary pharmacology & therapeutics, 2018, Volume: 48, Issue:4

    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.
    Human mutation, 1996, Volume: 8, Issue:4

    Topics: Anemia; Cells, Cultured; Consanguinity; Fatal Outcome; Female; Fibroblasts; Genotype; Humans; Infant

1996