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...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: 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.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Thoracic Society 2010
Konular:
D. Cystic Fibrosis
Online Erişim: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
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller