Liver Steatosis and Diarrhea After Liver Transplantation for Progressive Familial Intrahepatic Cholestasis Type 1: Can Biliary Diversion Solve These Problems?
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Gastroenterology,Pediatrics, Perinatology, and Child Health
Reference20 articles.
1. Progressive familial intrahepatic cholestasis;Bull;Clin Liver Dis,2018
2. Outcomes of surgical management of familial intrahepatic cholestasis 1 and bile export protein deficiencies;Bull;Hepatol Commun,2018
3. Progressive familial intrahepatic cholestasis type 1 and extrahepatic features: no catch-up of stature growth, exacerbation of diarrhea, and appearance of liver steatosis after liver transplantation;Lykavieris;J Hepatol,2003
4. Recovery of graft steatosis and protein-losing enteropathy after biliary diversion in a PFIC 1 liver transplanted child;Nicastro;Pediatr Transplant,2012
5. Living donor liver transplantation for progressive familial intrahepatic cholestasis type 1: two reported cases;Oya;Transplant Proc,2017
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