Outcomes of Childhood Cholestasis in Alagille Syndrome: Results of a Multicenter Observational Study

Alagille syndrome (ALGS) is an autosomal dominant multisystem disorder with cholestasis as a defining clinical feature. We sought to characterize hepatic outcomes in a molecularly defined cohort of children with ALGS‐related cholestasis. Two hundred and ninety‐three participants with ALGS with nativ...

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發表在:Hepatol Commun
Main Authors: Kamath, Binita M., Ye, Wen, Goodrich, Nathan P., Loomes, Kathleen M., Romero, Rene, Heubi, James E., Leung, Daniel H., Spinner, Nancy B., Piccoli, David A., Alonso, Estella M., Guthery, Stephen L., Karpen, Saul J., Mack, Cara L., Molleston, Jean P., Murray, Karen F., Rosenthal, Philip, Squires, James E., Teckman, Jeffrey, Wang, Kasper S., Thompson, Richard, Magee, John C., Sokol, Ronald J.
格式: Artigo
語言:Inglês
出版: John Wiley and Sons Inc. 2020
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Original Articles
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC7049675/
https://ncbi.nlm.nih.gov/pubmed/33313463
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/hep4.1468
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