Progressive Familial Intrahepatic Cholestasis: Is It Time to Transition to Genetic Cholestasis?
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Gastroenterology,Pediatrics, Perinatology, and Child Health
Reference26 articles.
1. Byler disease. Fatal familial intrahepatic cholestasis in an Amish kindred;Clayton;Am J Dis Child,1969
2. Clinical and biochemical findings in progressive familial intrahepatic cholestasis;Whitington;J Pediatr Gastroenterol Nutr,1994
3. Histologic pathology of the liver in progressive familial intrahepatic cholestasis;Alonso;J Pediatr Gastroenterol Nutr,1994
4. Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis;Houwen;Nat Genet,1994
5. Mapping of a locus for progressive familial intrahepatic cholestasis (Byler disease) to 18q21–q22, the benign recurrent intrahepatic cholestasis region;Carlton;Hum Mol Genet,1995
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Overview of Progressive Familial Intrahepatic Cholestasis;Clinics in Liver Disease;2022-08
2. Reply;Hepatology;2022-04-07
3. MYO5B Gene Mutations: A Not Negligible Cause of Intrahepatic Cholestasis of Infancy With Normal Gamma-Glutamyl Transferase Phenotype;Journal of Pediatric Gastroenterology & Nutrition;2022-02-04
4. Epatologia e gastroenterologia;Medico e Bambino;2021-07-31
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