Biliary atresia is a rare disease but remains the most common indication for pediatric liver transplantation as there are no effective medical therapies to slow progression after diagnosis. Variable contribution of genetic, immune, and environmental factors contributes to disease heterogeneity among patients with biliary atresia. Developing a deeper understanding of the disease mechanism will help to develop targeted medical therapies and improve patient outcomes.

Swati Antala

Sarah A. Taylor

Clinics in Liver Disease

肝病诊所是胃肠病学和肝病学领域咨询的完美来源，提供临床问题的答案、最新诊断方法和治疗的信息以及大量临床图像。每季度出版一期（2 月、5 月、8 月和 11 月），每期都提供专注于肝脏和胆道系统的深入评论。

Clinics in Liver Disease is a vital resource in the fields of gastroenterology and hepatology, offering answers to clinical questions, the latest diagnostic methods, and treatment information, along with a wealth of clinical images. Published quarterly (in February, May, August, and November), each issue provides in-depth reviews focused on the liver and biliary system.

《Clinics in Liver Disease》是胃肠病学和肝病学领域的重要参考来源，提供关于临床问题的解答、最新的诊断方法和治疗信息，以及丰富的临床图像。该期刊每季度出版一期（分别在2月、5月、8月和11月），每期专注于肝脏和胆道系统的深入评论。

Biliary Atresia in Children

Developing a deeper understanding of the disease mechanism will help to develop targeted medical therapies and improve patient outcomes.

Category	Quartile
医学	3
医学, 胃肠肝病学	4

Biliary Atresia in Children

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Journal Info

Category	Quartile
GASTROENTEROLOGY & HEPATOLOGY	2