Case 3 A New Category of Causes of Intrahepatic Cholestasis
Author:
Publisher
Informa UK Limited
Subject
Pathology and Forensic Medicine,Pediatrics, Perinatology and Child Health
Link
http://www.tandfonline.com/doi/pdf/10.3109/15513819209023305
Reference8 articles.
1. Familial giant cell hepatitis associated with synthesis of 3 beta, 7 alpha-dihydroxy-and 3 beta,7 alpha, 12 alpha-trihydroxy-5-cholenoic acids.
2. Lack of 3 beta-hydroxy-delta 5-C27-steroid dehydrogenase/isomerase in fibroblasts from a child with urinary excretion of 3 beta-hydroxy-delta 5-bile acids. A new inborn error of metabolism.
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1. Bile Acids and Bile Flow;Zakim and Boyer's Hepatology;2018
2. Inherited Intrahepatic Cholestatic Disorders and Disorders of Bilirubin Metabolism;2017
3. Mechanisms of Disease: inborn errors of bile acid synthesis;Nature Clinical Practice Gastroenterology & Hepatology;2008-06-24
4. Review article: the function and regulation of proteins involved in bile salt biosynthesis and transport;Alimentary Pharmacology & Therapeutics;2007-12-07
5. Inborn Errors of Bile Acid Metabolism;Seminars in Liver Disease;2007-08
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