The natural history of progressive fibrosing interstitial lung diseases

Abstract A proportion of patients with certain types of interstitial lung disease (ILD), including chronic hypersensitivity pneumonitis and ILDs associated with autoimmune diseases, develop a progressive fibrosing phenotype that shows similarities in clinical course to idiopathic pulmonary fibrosis....

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Bibliographic Details
Main Authors: Martin Kolb, Martina Vašáková
Format: Article
Language:English
Published: BMC 2019-03-01
Series:Respiratory Research
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12931-019-1022-1