Long-Term Outcome after Liver Transplantation for Progressive Familial Intrahepatic Cholestasis

Background and Objectives: Progressive familial intrahepatic cholestasis (PFIC) is a rare autosomal recessive inherited disease divided into five types (PFIC 1-5). Characteristic for all types is early disease onset, which may result clinically in portal hypertension, fibrosis, cirrhosis, hepatocell...

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Detalles Bibliográficos
Autores principales: Gül-Klein, Safak, Öllinger, Robert, Schmelzle, Moritz, Pratschke, Johann, Schöning, Wenzel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8400732/
https://www.ncbi.nlm.nih.gov/pubmed/34441060
http://dx.doi.org/10.3390/medicina57080854

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8400732/
https://www.ncbi.nlm.nih.gov/pubmed/34441060
http://dx.doi.org/10.3390/medicina57080854

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