Aim Biliary atresia (BA) literature has focussed on the relationship between age at Kasai
procedure (KP) and post‐KP outcomes. This study primarily examines post‐KP outcomes …

Biliary atresia (BA), a uniquely pediatric liver disease, is the leading cause of liver-related
death in children and the most frequent indication for liver transplantation in the pediatric …

Aim This study compared the outcomes of patients with biliary atresia (BA) treated according
to a standardised protocol with historical patients. Methods This is a single‐centred …

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 …

Objectives: Biliary atresia (BA) is a rare and progressive idiopathic disease affecting the
biliary tract that can lead to end-stage liver disease. The main treatment is Kasai …

Objectives Kasai portoenterostomy (KPE) is the treatment of choice for the fatal devastating
infantile type III biliary atresia (BA). The study aimed to analyze short-and long-term …

OBJECTIVE: To examine the outcome of biliary atresia (BA) and to identify prognostic factors
using a national database. STUDY DESIGN: All children born between January 1987 and …

Aim Biliary atresia (BA) has preponderance in Asian populations with Kasai
portoenterostomy (KP) regarded as the first‐line standard of care. Yet reports from Southeast …

Background A retrospective chart review of liver histologies in Kasai biliary atresia BA
patients operated 1/2017-7/2019 at our institution was conducted to identify histologic …

Biliary atresia (BA) is a childhood rare disease of the liver and bile ducts that requires
prompt surgical intervention. Age at surgery is an important prognostic factor; however …