Early Interstitial Lung Disease in Familial Pulmonary Fibrosis

Rationale: Identification of early, asymptomatic interstitial lung disease (ILD) in populations at risk of developing idiopathic pulmonary fibrosis (IPF) may improve the understanding of the natural history of IPF. Objectives: To determine clinical, radiographic, physiologic, and pathologic features...

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Detalhes bibliográficos
Main Authors: Rosas, Ivan O., Ren, Ping, Avila, Nilo A., Chow, Catherine K., Franks, Teri J., Travis, William D., McCoy, J. Philip, May, Rose M., Wu, Hai-Ping, Nguyen, Dao M., Arcos-Burgos, Mauricio, MacDonald, Sandra D., Gochuico, Bernadette R.
Formato: Artigo
Idioma:Inglês
Publicado em: American Thoracic Society 2007
Assuntos:
C. Interstitial Lung Disease
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1994234/
https://ncbi.nlm.nih.gov/pubmed/17641157
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1164/rccm.200702-254OC
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