Association of Lung Function, Chest Radiographs and Clinical Features in Infants with Cystic Fibrosis

BACKGROUND: The optimal strategy for monitoring cystic fibrosis (CF) lung disease in infancy remains unclear. OBJECTIVE: To describe longitudinal associations between infant pulmonary function tests (iPFTs), chest radiograph (CXR) scores and other characteristics. METHODS: CF patients ≤ 24 months ol...

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Главные авторы: Rosenfeld, Margaret, Farrell, Philip M., Kloster, Margaret, Swanson, Jonathan O., Vu, Thuy, Brumback, Lyndia, Acton, James D., Castile, Robert G., Colin, Andrew A., Conrad, Carol K., Hart, Meeghan A., Kerby, Gwendolyn S., Hiatt, Peter W., Mogayzel, Peter J., Johnson, Robin C., Davis, Stephanie D.
Формат: Artigo
Язык:Inglês
Опубликовано: 2013
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Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC3795977/
https://ncbi.nlm.nih.gov/pubmed/23722613
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1183/09031936.00138412
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