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Paper Details

Neonatal Gastrointestinal and Respiratory Microbiome in Cystic Fibrosis: Potential Interactions and Implications for Systemic Health.
Clinical Therapeutics
18
2016
CF, CFTR, CFTR mutations, Cystic Fibrosis, Cystic fibrosis, Cystic fibrosis (CF) transmembrane conductance regulator, Dysbiosis, children, chronic infection, dysbiosis of the gastrointestinal and respiratory microsystems, dysregulation of immune function, growth failure, infants, respiratory and systemic morbidity, undernutrition
Author NameAffiliation
Juliette C MadanChildren's Hospital at Dartmouth, Geisel School of Medicine at Dartmouth
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Datasets

Release 1.2