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The natural history of progressive fibrosing interstitial lung diseases

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. Irrespec...

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Bibliografske podrobnosti
izdano v:Respir Res
Main Authors: Kolb, Martin, Vašáková, Martina
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2019
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6417262/
https://ncbi.nlm.nih.gov/pubmed/30871560
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12931-019-1022-1
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