Combined pulmonary fibrosis and emphysema: a distinct underrecognised entity

By V. Cottin, H. Nunes, P. Brillet, P. Delaval, G. Devouassoux, I. Tillie‐Leblond, D. Israel‐Biet, I. Court-Fortune, D. Valeyre, J. Cordier. European Respiratory Journal, 2005

939 citations recorded by the source corpus.

Subfields: Pulmonary and Respiratory Medicine

View Paper: https://www.semanticscholar.org/paper/e9562b14d21e8f35f1e5127d50d63bd100aeeed5

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In Pulmonary and Respiratory Medicine

1. H. Collard
2. B. Ley
3. T. King
4. G. Simonneau

Citations in the corpus

• Pulmonary arterial hypertension (2013, background): “A category of lung disease characterized by a mixed obstructive and restrictive pattern was added, including chronic bronchiectasis, cystic fibrosis and the recently described syndrome of combined pulmonary fibrosis and emphysema in which the prevalence of PH is almost 50% [66,67].”
• Clinical course and prediction of survival in idiopathic pulmonary fibrosis. (2011, background): “Emphysema affects the baseline pulmonary function tests by increasing lung volumes and decreasing DLCO and FEV1/FVC, as well as altering the change of these values over time, and therefore altering or masking the assessment of disease severity at baseline and progression over time (72, 73).”