Cholestasis After Pediatric Liver Transplantation–Recurrence of a Progressive Familial Intrahepatic Cholestasis Phenotype as a Rare Differential Diagnosis: A Case Report-Reference-Cited by-同舟云学术

Cholestasis After Pediatric Liver Transplantation–Recurrence of a Progressive Familial Intrahepatic Cholestasis Phenotype as a Rare Differential Diagnosis: A Case Report

Published:2017-09 Issue:7 Volume:49 Page:1628-1633
ISSN:0041-1345
Container-title:Transplantation Proceedings
language:en
Short-container-title:Transplantation Proceedings

Author:

Prusinskas B.,Kathemann S.,Pilic D.,Hegen B.,Küster P.,Keitel V.,Häussinger D.,Büscher R.,Baba H.A.,Hoyer P.F.,Lainka E.

Publisher

Elsevier BV

Subject

Transplantation,Surgery

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3. Severe bile salt export pump deficiency: 82 different ABCB11 mutations in 109 families;Straunieks;Gastroenterology,2008

4. Progressive familial intrahepatic cholestasis related to mutation of the TJP2 gene: recent advances;Zhang;Zhonghua Gan Zang Bing Za Zhi,2016

5. Mutations in the nuclear bile acid receptor FXR cause progressive familial intrahepatic cholestasis;Gomez-Ospina;Nat Commun,2016

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