Modeling Outcomes in Children With Biliary Atresia With Native Liver After 2 Years of Age

Veena Venkat, Vicky L. Ng, John C. Magee, Wen Ye, Kieran Hawthorne, Sanjiv Harpavat, Jean P. Molleston, Karen F. Murray, Kasper S. Wang, Nisreen Soufi, Lee M. Bass, Estella M. Alonso, Jorge A. Bezerra, M. Kyle Jensen, Binita M. Kamath, Kathleen M. Loomes, Cara L. Mack, Philip Rosenthal, Benjamin L. Shneider, Robert H. Squires, Ronald J. Sokol, Saul J. Karpen, for the Childhood Liver Disease Research Network – 3 October 2020 – Approximately 50% of infants with biliary atresia (BA) undergoing Kasai portoenterostomy show survival with native liver (SNL) at age 2 years.

Analysis of Survival Benefits of Living Versus Deceased Donor Liver Transplant in High Model for End‐Stage Liver Disease and Hepatorenal Syndrome

Tiffany Cho‐Lam Wong, James Yan‐Yue Fung, Herbert H. Pang, Calvin Ka‐Lam Leung, Hoi‐Fan Li, Sui‐Ling Sin, Ka‐Wing Ma, Brian Wong‐Hoi She, Jeff Wing‐Chiu Dai, Albert Chi‐Yan Chan, Tan‐To Cheung, Chung‐Mau Lo – 2 October 2020

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