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Modeling Outcomes in Children With Biliary Atresia With Native Liver After 2 Years of Age
Approximately 50% of infants with biliary atresia (BA) undergoing Kasai portoenterostomy show survival with native liver (SNL) at age 2 years. Predictors of disease progression after age 2 years are unknown, despite estimates of 20%‐30% undergoing liver transplant (LT) between age 2 and 18 years. We...
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| Vydáno v: | Hepatol Commun |
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| Hlavní autoři: | , , , , , , , , , , , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
John Wiley and Sons Inc.
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7706301/ https://ncbi.nlm.nih.gov/pubmed/33305153 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/hep4.1602 |
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