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Paper Details

Clinical Variability After Partial External Biliary Diversion in Familial Intrahepatic Cholestasis 1 Deficiency.
J Pediatr Gastroenterol Nutr
14
2017
ATP8B1 gene, FIC1, FIC1 deficient, FIC1 disease, Familial Intrahepatic Cholestasis 1 Deficiency, Familial intrahepatic cholestasis 1 (FIC1) deficiency, PEBD, Splenomegaly, aminotransferase, aspartate, aspartate aminotransferase, benign recurrent intrahepatic cholestasis, bilirubin, cholestasis, cholestatic, cholestatic episodes, cholestatic events, itching, liver disease, patient, patients, pruritus, splenomegaly
Author NameAffiliation
James E SquiresThomas E. Starzl Transplantation Institute, Hillman Center for Pediatric Transplantation, Children's Hospital of Pittsburgh of University of Pittsburgh Medical Center, Baylor College of Medicine
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Release 1.2