The yin and yang of idiopathic pulmonary fibrosis

Affiliations

¹ Center for interstitial and rare lung diseases, Pneumology and respiratory critical care medicine, Thoraxklinik, University of Heidelberg, Heidelberg, Germany and Translational Lung Research Center Heidelberg, Member of the German Center for Lung Research (DZL) kreuter@uni-heidelberg.de.
² Dept of Pulmonary Medicine and National Reference Center for Rare Pulmonary Diseases, Competence Center for Pulmonary Arterial Hypertension, Louis Pradel Hospital, Hospices Civils de Lyon, Claude Bernard Lyon 1 University, Lyon, France.

Free article

Editorial

Michael Kreuter et al. Eur Respir J. 2017.

Free article

. 2017 Feb 23;49(2):1602316.

doi: 10.1183/13993003.02316-2016. Print 2017 Feb.

¹ Center for interstitial and rare lung diseases, Pneumology and respiratory critical care medicine, Thoraxklinik, University of Heidelberg, Heidelberg, Germany and Translational Lung Research Center Heidelberg, Member of the German Center for Lung Research (DZL) kreuter@uni-heidelberg.de.
² Dept of Pulmonary Medicine and National Reference Center for Rare Pulmonary Diseases, Competence Center for Pulmonary Arterial Hypertension, Louis Pradel Hospital, Hospices Civils de Lyon, Claude Bernard Lyon 1 University, Lyon, France.

No abstract available

Comment on

Baseline characteristics of idiopathic pulmonary fibrosis: analysis from the Australian Idiopathic Pulmonary Fibrosis Registry.
Jo HE, Glaspole I, Grainge C, Goh N, Hopkins PM, Moodley Y, Reynolds PN, Chapman S, Walters EH, Zappala C, Allan H, Keir GJ, Hayen A, Cooper WA, Mahar AM, Ellis S, Macansh S, Corte TJ. Jo HE, et al. Eur Respir J. 2017 Feb 23;49(2):1601592. doi: 10.1183/13993003.01592-2016. Print 2017 Feb. Eur Respir J. 2017. PMID: 28232409