Evolution of lung function during the first year of life in newborn screened cystic fibrosis infants

RATIONALE: Newborn screening (NBS) for cystic fibrosis (CF) allows early intervention. Design of randomised controlled trials (RCT) is currently impeded by uncertainty regarding evolution of lung function, an important trial end point in such infants. OBJECTIVE: To assess changes in pulmonary functi...

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Bibliographische Detailangaben
Hauptverfasser: Nguyen, The Thanh-Diem, Thia, Lena P, Hoo, Ah-Fong, Bush, Andrew, Aurora, Paul, Wade, Angie, Chudleigh, Jane, Lum, Sooky, Stocks, Janet
Format: Artigo
Sprache:Inglês
Veröffentlicht: BMJ Publishing Group 2014
Schlagworte:
Cystic Fibrosis
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4174068/
https://ncbi.nlm.nih.gov/pubmed/24072358
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/thoraxjnl-2013-204023
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