Results 91 to 100 of about 3,364 (172)

UEG Week 2025 Moderated Posters

open access: yes
United European Gastroenterology Journal, Volume 13, Issue S8, Page S189-S802, October 2025.
wiley   +1 more source

UEG Week 2025 Poster Presentations

open access: yes
United European Gastroenterology Journal, Volume 13, Issue S8, Page S803-S1476, October 2025.
wiley   +1 more source

Abstract

open access: yes
JPGN Reports, Volume 6, Issue S2, Page S1-S814, September 2025.
wiley   +1 more source

A Case Report of Dublin-Johnson Syndrome

open access: yesپزشکی بالینی ابن سینا, 2000
Hyperbilirubinemia is a common manifestation in internal medicine. It is divided to conjugated and unconjugated hyperbilirubinemia . Conjugated hyperbilirubinemia usually results from hepatocellular or cholestatic liver disease or from extrahepatic ...
Amir Hooshang Mohammad Alizadeh
doaj  

Identification of a Locus for Progressive Familial Intrahepatic Cholestasis PFIC2on Chromosome 2q24

open access: yes, 1997
SummaryProgressive familial intrahepatic cholestasis (PFIC; OMIM 211600) is the second most common familial cholestatic syndrome presenting in infancy. A locus has previously been mapped to chromosome 18q21-22 in the original Byler pedigree.
Strautnieks, Sandra S.   +8 more
core   +1 more source

Bile formation and cholestasis

open access: yes, 2000
Transport proteins in hepatocytes and bile duct epithelium mediate uptake and secretion of cholephilic compounds in the liver and are involved in bile formation. - Many of these proteins have recently been cloned and characterized and appear to belong to
Jansen, P. L.M.   +2 more
core   +2 more sources

Benign Recurrent Intrahepatic Cholestasis — Unravelleing the Paradox

open access: yesIndian Pediatrics, 2021
R, Ganesh   +3 more
openaire   +2 more sources

[Recurrent benign intrahepatic cholestasis and their progression to familiar progressive intrahepatic cholestasis].

open access: yesRevista de gastroenterologia del Peru : organo oficial de la Sociedad de Gastroenterologia del Peru, 2008
Benign recurrent intrahepatic cholestasis (BRIC) is a rare form of intrahepatic cholestasis characterized by repeated self-limited episodes of severe pruritus and jaundice. Classically its natural evolution is benign, without progress to fibrosis or hepatic insufficiency; although, lastly were reported cases which progress to Progressive familial ...
Marco, Alburquerque Miranda   +5 more
openaire   +1 more source

Recurrent Cholestatic Jaundice – Think beyond Viral Hepatitis

open access: yes, 2014
- We report a case of recurrent intrahepatic cholestasis in an 4-year-old boy who developed four episodes of purities and jaundice at the ages of 6months, 1yr 2yr and 4 years.
Anil Kumar Y. C, N. Chowdareddy, Er B
core  

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