Biliary atresia is a severe cholangiopathy of early infancy that destroys extrahepatic bile
ducts and disrupts bile flow. With a poorly defined disease pathogenesis, treatment consists …

Despite decades since its description and decades of intensive researches, cause of biliary
atresia disease remains enigmatic. The inheritance of biliary atresia is not Mendelian …

Biliary atresia (BA) is a rapidly progressive and destructive fibrotic disorder of unknown
etiology affecting the extrahepatic biliary tree of neonates. Epidemiological studies suggest …

Biliary atresia (BA) is a rare pediatric cholangiopathy characterized by fibrosclerosing
obliteration of the extrahepatic bile ducts, leading to cholestasis, fibrosis, cirrhosis, and …

Abstract Background Human enterovirus 71 (EV71) is an important pathogen caused large
outbreaks in Asian-Pacific region with severe neurological complications and may lead to …

Background & Aims Biliary atresia (BA) is a rare and most severe cholestatic disease in
neonates, but the pathogenic mechanisms are unknown. Through a previous genome wide …

Abstract In the United States, biliary atresia (BA) is the most frequent indication for liver
transplantation in pediatric patients. BA is a complex disease, with suspected environmental …

Biliary atresia is a severe obliterative cholangiopathy in early infancy that is by far the most
common cause of surgical jaundice and the most common indicator for liver transplantation …

Objectives: Biliary atresia (BA) is a progressive fibroinflammatory cholangiopathy affecting
the bile ducts of neonates. Although BA is the leading indication for pediatric liver …

Background & Aims Biliary atresia (BA) is poorly understood and leads to liver
transplantation (LT), with the requirement for and associated risks of lifelong …