A Nomogram Predicting the Prognosis of Children With Biliary Atresia After Hepatoportoenterostomy

Background: Although Kasai portoenterostomy (KPE) is performed timely for most children with biliary atresia (BA), the native liver survival (NLS) is still poor due to the progressive liver fibrosis. Many children have to receive liver transplantation (LT) within 2 years after KPE. Early prediction...

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Detalles Bibliográficos
Autores principales: Liu, Jin-qiao, Chen, Wen-juan, Zhou, Meng-jie, Li, Wen-feng, Tang, Ju, Zhou, Qi-chang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943446/
https://www.ncbi.nlm.nih.gov/pubmed/33718307
http://dx.doi.org/10.3389/fped.2021.641318

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943446/
https://www.ncbi.nlm.nih.gov/pubmed/33718307
http://dx.doi.org/10.3389/fped.2021.641318

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