Caroli's Disease: Current Knowledge of Its Biliary Pathogenesis Obtained from an Orthologous Rat Model

Caroli's disease belongs to a group of hepatic fibropolycystic diseases and is a hepatic manifestation of autosomal recessive polycystic kidney disease (ARPKD). It is a congenital disorder characterized by segmental saccular dilatations of the large intrahepatic bile duct and is frequently asso...

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Detalles Bibliográficos
Autores principales: Sato, Yasunori, Ren, Xiang Shan, Nakanuma, Yasuni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3168917/
https://www.ncbi.nlm.nih.gov/pubmed/22007315
http://dx.doi.org/10.1155/2012/107945

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3168917/
https://www.ncbi.nlm.nih.gov/pubmed/22007315
http://dx.doi.org/10.1155/2012/107945

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