Fecal dysbiosis in infants with cystic fibrosis is associated with early linear growth failure

Most infants with cystic fibrosis (CF) have pancreatic exocrine insufficiency that results in nutrient malabsorption and requires oral pancreatic enzyme replacement. Newborn screening for CF has enabled earlier diagnosis, nutritional intervention, and enzyme replacement for these infants, allowing m...

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Опубликовано в: :Nat Med
Главные авторы: Hayden, HS, Eng, A, Pope, CE, Brittnacher, MJ, Vo, AT, Weiss, EJ, Hager, KR, Martin, BD, Leung, DH, Heltshe, SL, Borenstein, E, Miller, SI, Hoffman, LR
Формат: Artigo
Язык:Inglês
Опубликовано: 2020
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Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC7018602/
https://ncbi.nlm.nih.gov/pubmed/31959989
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41591-019-0714-x
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