Caroli′ s Disease: Current Knowledge of Its Biliary Pathogenesis Obtained from an Orthologous Rat Model
Y Sato, XS Ren, Y Nakanuma - International journal of …, 2012 - Wiley Online Library
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 …
manifestation of autosomal recessive polycystic kidney disease (ARPKD). It is a congenital …
[PDF][PDF] Caroli's Disease: Current Knowledge of Its Biliary Pathogenesis Obtained from an Orthologous Rat Model
Y Sato, XS Ren, Y Nakanuma - 2012 - cyberleninka.org
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 …
manifestation of autosomal recessive polycystic kidney disease (ARPKD). It is a congenital …
[PDF][PDF] Caroli's Disease: Current Knowledge of Its Biliary Pathogenesis Obtained from an Orthologous Rat Model
Y Sato, XS Ren, Y Nakanuma - 2012 - researchgate.net
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 …
manifestation of autosomal recessive polycystic kidney disease (ARPKD). It is a congenital …
Caroli's Disease: Current Knowledge of Its Biliary Pathogenesis Obtained from an Orthologous Rat Model
Y Sato, XS Ren, Y Nakanuma - International journal of …, 2012 - pubmed.ncbi.nlm.nih.gov
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 …
manifestation of autosomal recessive polycystic kidney disease (ARPKD). It is a congenital …
Caroli's Disease: Current Knowledge of Its Biliary Pathogenesis Obtained from an Orthologous Rat Model
Y Sato, XS Ren, Y Nakanuma - 2012 - kanazawa-u.repo.nii.ac.jp
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 …
manifestation of autosomal recessive polycystic kidney disease (ARPKD). It is a congenital …
Caroli's Disease: Current Knowledge of Its Biliary Pathogenesis Obtained from an Orthologous Rat Model.
Y Sato, XS Ren, Y Nakanuma - International Journal of …, 2012 - search.ebscohost.com
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 …
manifestation of autosomal recessive polycystic kidney disease (ARPKD). It is a congenital …
Caroli's Disease: Current Knowledge of Its Biliary Pathogenesis Obtained from an Orthologous Rat Model
Y Sato, XS Ren, Y Nakanuma - International Journal of Hepatology, 2012 - cir.nii.ac.jp
抄録 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 …
manifestation of autosomal recessive polycystic kidney disease (ARPKD). It is a congenital …
[PDF][PDF] Caroli's Disease: Current Knowledge of Its Biliary Pathogenesis Obtained from an Orthologous Rat Model
Y Sato, XS Ren, Y Nakanuma - 2012 - pdfs.semanticscholar.org
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 …
manifestation of autosomal recessive polycystic kidney disease (ARPKD). It is a congenital …
[PDF][PDF] Caroli's Disease: Current Knowledge of Its Biliary Pathogenesis Obtained from an Orthologous Rat Model
Y Sato, XS Ren, Y Nakanuma - 2012 - scienceopen.com
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 …
manifestation of autosomal recessive polycystic kidney disease (ARPKD). It is a congenital …
[HTML][HTML] Caroli's Disease: Current Knowledge of Its Biliary Pathogenesis Obtained from an Orthologous Rat Model
Y Sato, XS Ren, Y Nakanuma - International Journal of Hepatology, 2012 - ncbi.nlm.nih.gov
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 …
manifestation of autosomal recessive polycystic kidney disease (ARPKD). It is a congenital …