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...

תיאור מלא

שמור ב:
מידע ביבליוגרפי
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.
פורמט: Artigo
שפה:Inglês
יצא לאור: American Thoracic Society 2010
נושאים:
D. Cystic Fibrosis
גישה מקוונת: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
תגים: הוספת תג
אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!

פריטים דומים