Biliary atresia presents as an obliterative cholangiopathy with neonatal jaundice and pale
stools. The disease exhibits aetiological heterogeneity with a multiplicity of potential …

Biliary atresia (BA) is a rare cholangiopathy of infancy in which the bile ducts obliterate,
leading to profound cholestasis and liver fibrosis. BA is hypothesized to be caused by a viral …

Objectives: This study analyses the prognosis of biliary atresia (BA) in France since 1986,
when both Kasai operation (KOp) and liver transplantation (LT) became widely available …

Recent developments in paediatric gastrointestinal surgery have focused on minimally
invasive surgery, the accumulation of high-quality clinical evidence, and scientific research …

Biliary atresia (BA) is a common cause of surgical jaundice during the neonatal period. It is
currently considered as a spectrum of diseases with a common final pathology characterized …

Biliary atresia (BA) is a rare and severe inflammatory and obliterative cholangiopathy that
affects both extra-and intrahepatic bile ducts. BA symptoms occur shortly after birth with …

Biliary atresia is characterised as an obliterative cholangiopathy of both extra-and intra-
hepatic bile ducts. There is marked aetiological heterogeneity with a number of different …

The use of adjuvant steroids following Kasai porteoenterostomy (KPE) for biliary atresia is
controversial. The aim of this study was twofold: a systematic review of published literature …

Background/purpose Biliary atresia is the most common reason for newborn cholestasis and
pediatric liver transplantation. Even after normalization of serum bilirubin after …

Portoenterostomy (PE) has remained as the generally accepted first line surgical treatment
for biliary atresia (BA) for over 50 years. Currently, close to half of BA patients survive …