Extrahepatic manifestations of progressive familial intrahepatic cholestasis syndromes: Presentation of a case series and literature review-Reference-Cited by-同舟云学术

Extrahepatic manifestations of progressive familial intrahepatic cholestasis syndromes: Presentation of a case series and literature review

Published:2022-03-15 Issue:5 Volume:42 Page:1084-1096
ISSN:1478-3223
Container-title:Liver International
language:en
Short-container-title:Liver International

Author:

Pfister Eva‐Doreen¹^ORCID,Dröge Carola²³,Liebe Roman²^ORCID,Stalke Amelie¹⁴^ORCID,Buhl Nicole¹⁴,Ballauff Antje⁵,Cantz Tobias⁶,Bueltmann Eva⁷,Stindt Jan²,Luedde Tom²,Baumann Ulrich¹⁸,Keitel Verena²³^ORCID

Affiliation:

1. Division of Paediatric Gastroenterology and Hepatology, Department of Paediatric Liver, Kidney and Metabolic Diseases Hannover Medical School Hannover Germany

2. Department of Gastroenterology, Hepatology and Infectious Diseases, University Hospital Düsseldorf Medical Faculty of Heinrich Heine University Düsseldorf Düsseldorf Germany

3. Department of Gastroenterology, Hepatology and Infectious Diseases, University Hospital Magdeburg Medical Faculty of Otto von Guericke University Magdeburg Germany

4. Department of Human Genetics Hannover Medical School Hannover Germany

5. Department of Paediatrics Helios Hospital Krefeld Germany

6. Translational Hepatology and Stem Cell Biology, Department of Gastroenterology, Hepatology and Endocrinology, REBIRTH‐Center for Translational Regenerative Medicine Hannover Medical School Hannover Germany

7. Institute of Diagnostic and Interventional Neuroradiology Hannover Medical School Hannover Germany

8. Institute of Immunology and Immunotherapy University of Birmingham Birmingham UK

Funder

Bundesministerium für Bildung und Forschung

Publisher

Wiley

Subject

Hepatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/liv.15200

Reference69 articles.

1. Molecular characterization and structural implications of 25 new ABCB4 mutations in progressive familial intrahepatic cholestasis type 3 (PFIC3)