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Autor:
Amy Lowichik, Catalina Jaramillo, Stephen L. Guthery, Yang Li, Taegun Kim, Michael Kyle Jensen, Gregory J. Stoddard
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 70:87-92
Background/rationale Biliary atresia (BA) is a cholangiopathy characterized by bile flow obstruction due to destruction of the biliary tree. Without surgical correction with Kasai portoenterostomy (KPE), BA leads to death or liver transplant (LTx). E