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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| Main Authors: | , , , , , |
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| Format: | Book |
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Frontiers Media S.A.,
2021-02-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |