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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Autores principales: 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.
Formato: Artigo
Lenguaje:Inglês
Publicado: 2013
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Article
Acceso en línea: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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