Multicenter Evaluation of Infant Lung Function Tests as Cystic Fibrosis Clinical Trial Endpoints

Rationale: The conducting of clinical trials in infants with cystic fibrosis (CF) has been hindered by lack of sensitive outcome measures. Objectives: To evaluate safety, feasibility, and ability to detect abnormalities in lung function of serial pulmonary function tests (PFTs) in infants with CF. M...

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Detalhes bibliográficos
Main Authors: Davis, Stephanie D., Rosenfeld, Margaret, Kerby, Gwendolyn S., Brumback, Lyndia, Kloster, Margaret H., Acton, James D., Colin, Andrew A., Conrad, Carol K., Hart, Meeghan A., Hiatt, Peter W., Mogayzel, Peter J., Johnson, Robin C., Wilcox, Stephanie L., Castile, Robert G.
Formato: Artigo
Idioma:Inglês
Publicado em: American Thoracic Society 2010
Assuntos:
D. Cystic Fibrosis
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3159081/
https://ncbi.nlm.nih.gov/pubmed/20622043
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1164/rccm.200908-1236OC
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