Predictors of Successful Kasai Portoenterostomy and Survival with Native Liver at 2 Years in Infants with Biliary Atresia

OBJECTIVES: Kasai portoenterostomy (KPE) is the primary treatment for biliary atresia (BA) with subsequent liver transplantation in failed cases. The aim of this work was to study the outcome of KPE in children with BA and identify the factors predicting a successful KPE. METHODS: Children diagnosed...

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Bibliografiset tiedot
Julkaisussa:J Clin Exp Hepatol
Päätekijät: Kumar, Ruchika, Lal, Bikrant B., Sood, Vikrant, Khanna, Rajeev, Kumar, Senthil, Bharathy, Kishore G.S., Alam, Seema
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Elsevier 2019
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Original Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6728523/
https://ncbi.nlm.nih.gov/pubmed/31516261
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jceh.2018.09.008
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