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Odevixibat after liver transplant in patients with progressive familial intrahepatic cholestasis type 1: A case series. [PDF]
Vogel GF +13 more
europepmc +1 more source
Implantation of nasobiliary drainage in treatment of severe episodes of benign recurrent intrahepatic cholestasis (BRIC) in pediatric patients. [PDF]
Dądalski M +7 more
europepmc +1 more source
Erratum to "A sporadic case of benign recurrent intrahepatic cholestasis in a growth-impaired young male". [PDF]
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Bailliere's Best Practice and Research in Clinical Gastroenterology, 2010
Progressive familial intrahepatic cholestasis (PFIC) type 1, 2 and 3 are due to mutations in ATP8B1, ABCB11 and ABCB4, respectively. Each of these genes encodes a hepatocanalicular transporter, which is essential for the proper formation of bile. Mutations in ABCB4 can result in progressive cholestatic disease, while mutations in ATP8B1 and ABCB11 can ...
Saskia W C Van Mil +2 more
exaly +4 more sources
Progressive familial intrahepatic cholestasis (PFIC) type 1, 2 and 3 are due to mutations in ATP8B1, ABCB11 and ABCB4, respectively. Each of these genes encodes a hepatocanalicular transporter, which is essential for the proper formation of bile. Mutations in ABCB4 can result in progressive cholestatic disease, while mutations in ATP8B1 and ABCB11 can ...
Saskia W C Van Mil +2 more
exaly +4 more sources
Intrahepatic cholestasis of pregnancy
Česká gynekologieObjective: The aim of this work is to summarize current scientific information focusing on the diagnosis, management, and treatment of intrahepatic cholestasis in pregnancy according to available literature. Methodology: Literature sources were searched using the Web of Science, Scopus, and PubMed/Medline databases.
Luděk, Kostka +2 more
+9 more sources
Intrahepatic Cholestasis of Pregnancy
Clinical Obstetrics & Gynecology, 2020Intrahepatic cholestasis of pregnancy is a common disorder of pregnancy manifested by pruritus and elevated bile acids. The etiology of cholestasis is poorly understood and management is difficult due to the paucity of data regarding its diagnosis, treatment, and related adverse outcomes.
Devin D, Smith, Kara M, Rood
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Intrahepatic Cholestasis in Childhood
New England Journal of Medicine, 1976The apparent well-being of some children who as neonates were believed to have obstructive jaundice prompted us to study the clinical course, histologic features and possible etiologic factors in 17 children with cholestasis in the neonatal period. During a follow-up period of five months to 22 years, all had signs of chronic cholestasis, but only four
J, Heathcote +3 more
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