Progressive familial intrahepatic cholestasis and inborn errors of bile acid synthesis
Author:
Publisher
Elsevier BV
Subject
Gastroenterology,Hepatology
Reference5 articles.
1. Progressive familial intrahepatic cholestasis;Davit-Spraul;Orphanet J Rare Dis,2009
2. Differences in presentation and progression between severe FIC1 and BSEP deficiencies;Pawlikowska;J Hepatol,2010
3. Partial external diversion of bile for the treatment of intractable pruritus associated with intrahepatic cholestasis;Whitington;Gastroenterology,1988
4. Disorders of bile acid synthesis;Clayton;J Inherit Metab Dis,2011
5. Oral cholic acid for hereditary defects of primary bile acid synthesis: a safe and effective long-term therapy;Gonzales;Gastroenterology,2009
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1. A female of progressive familial intrahepatic cholestasis type 3 caused by heterozygous mutations of ABCB4 gene and her cirrhosis improved after treatment of ursodeoxycholic acid: a case report;BMC Medical Genomics;2023-07-25
2. Byler’s disease in a young child (own clinical observation);Karnataka Paediatric Journal;2022-11-16
3. Nutritional Management of Children with Liver Disease;Textbook of Pediatric Gastroenterology, Hepatology and Nutrition;2021-11-25
4. Familial Intrahepatic Cholestasis;Textbook of Pediatric Gastroenterology, Hepatology and Nutrition;2021-11-25
5. Inborn Errors of Metabolism and the Gastrointestinal Tract;Gastroenterology Clinics of North America;2019-06
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