Infants with cystic fibrosis have altered fecal functional capacities with potential clinical and metabolic consequences

BACKGROUND: Infants with cystic fibrosis (CF) suffer from gastrointestinal (GI) complications, including pancreatic insufficiency and intestinal inflammation, which have been associated with impaired nutrition and growth. Recent evidence identified altered fecal microbiota taxonomic compositions in...

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Detalles Bibliográficos
Autores principales: Eng, Alexander, Hayden, Hillary S., Pope, Christopher E., Brittnacher, Mitchell J., Vo, Anh T., Weiss, Eli J., Hager, Kyle R., Leung, Daniel H., Heltshe, Sonya L., Raftery, Daniel, Miller, Samuel I., Hoffman, Lucas R., Borenstein, Elhanan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8444586/
https://www.ncbi.nlm.nih.gov/pubmed/34525965
http://dx.doi.org/10.1186/s12866-021-02305-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8444586/
https://www.ncbi.nlm.nih.gov/pubmed/34525965
http://dx.doi.org/10.1186/s12866-021-02305-z

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