1-anilino-8-naphthalenesulfonate has been researched along with Bronze Diabetes in 5 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 | 1 (20.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 2 (40.00) | 24.3611 |
2020's | 2 (40.00) | 2.80 |
Authors | Studies |
---|---|
Seeßle, J | 1 |
Gan-Schreier, H | 1 |
Kirchner, M | 1 |
Stremmel, W | 1 |
Chamulitrat, W | 1 |
Merle, U | 2 |
Buch, S | 1 |
Sharma, A | 1 |
Ryan, E | 1 |
Datz, C | 1 |
Griffiths, WJH | 1 |
Way, M | 1 |
Buckley, TWM | 1 |
Ryan, JD | 1 |
Stewart, S | 1 |
Wright, C | 1 |
Dongiovanni, P | 3 |
Fracanzani, A | 1 |
Zwerina, J | 1 |
Weiss, KH | 1 |
Aigner, E | 1 |
Krones, E | 1 |
Dejaco, C | 1 |
Fischer, J | 1 |
Berg, T | 1 |
Valenti, L | 3 |
Zoller, H | 1 |
McQuillin, A | 1 |
Hampe, J | 1 |
Stickel, F | 1 |
Morgan, MY | 1 |
Donati, B | 1 |
Fares, R | 1 |
Lombardi, R | 1 |
Mancina, RM | 1 |
Romeo, S | 1 |
Maggioni, P | 1 |
Piperno, A | 1 |
Rametta, R | 1 |
Pelucchi, S | 1 |
Mariani, R | 1 |
Fracanzani, AL | 1 |
Fargion, S | 1 |
Simon, M | 1 |
Gosselin, M | 1 |
Kerbaol, M | 1 |
Delanoe, G | 1 |
Trebaul, L | 1 |
Bourel, M | 1 |
1 review available for 1-anilino-8-naphthalenesulfonate and Bronze Diabetes
Article | Year |
---|---|
PNPLA3 I148M polymorphism and progressive liver disease.
Topics: Carcinoma, Hepatocellular; Cholangitis, Sclerosing; Disease Progression; Fatty Liver; Fatty Liver, A | 2013 |
4 other studies available for 1-anilino-8-naphthalenesulfonate and Bronze Diabetes
Article | Year |
---|---|
Plasma Lipidome, PNPLA3 polymorphism and hepatic steatosis in hereditary hemochromatosis.
Topics: Cohort Studies; Hemochromatosis; Humans; Iron Overload; Lipase; Lipidomics; Liver; Membrane Proteins | 2020 |
Variants in PCSK7, PNPLA3 and TM6SF2 are risk factors for the development of cirrhosis in hereditary haemochromatosis.
Topics: Europe; Genotype; Hemochromatosis; Humans; Lipase; Liver Cirrhosis; Membrane Proteins; Non-alcoholic | 2021 |
Patatin-like phospholipase domain containing-3 gene I148M polymorphism, steatosis, and liver damage in hereditary hemochromatosis.
Topics: Adult; Biomarkers; Biopsy; Chi-Square Distribution; Disease Progression; Fatty Liver; Female; Gene F | 2012 |
Functional study of exocrine pancreas in idiopathic hemochromatosis, untreated and treated by venesections.
Topics: Adult; Aged; Bicarbonates; Bloodletting; Cholecystokinin; Duodenum; Female; Hemochromatosis; Humans; | 1973 |