Baseline Analysis of a Young Alpha-1-AT Deficiency Liver Disease Cohort Reveals Frequent Portal Hypertension

OBJECTIVE: Alpha-1-antitrypsin deficiency (A1AT) is a common genetic disease with unpredictable and highly variable course. The Childhood Liver Disease Research and Education Network (ChiLDREN) is an NIH, multi-center, longitudinal consortium studying pediatric liver diseases, with the objective of...

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Publicado no:J Pediatr Gastroenterol Nutr
Main Authors: Teckman, Jeffrey H, Rosenthal, Philip, Abel, Robert, Bass, Lee M., Michail, Sonia, Murray, Karen F., Rudnick, David A., Thomas, Daniel W., Spino, Cathie, Arnon, Ronen, Hertel, Paula M., Heubi, James, Kamath, Binita M., Karnsakul, Wikrom, Loomes, Kathleen M., Magee, John C., Molleston, Jean P., Romero, Rene, Shneider, Benjamin L, Sherker, Averell H, Sokol, Ronald J
Formato: Artigo
Idioma:Inglês
Publicado em: 2015
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4692167/
https://ncbi.nlm.nih.gov/pubmed/25651489
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MPG.0000000000000753
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