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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Detalles Bibliográficos
Autores principales: Kolb, Martin, Vašáková, Martina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6417262/
https://www.ncbi.nlm.nih.gov/pubmed/30871560
http://dx.doi.org/10.1186/s12931-019-1022-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6417262/
https://www.ncbi.nlm.nih.gov/pubmed/30871560
http://dx.doi.org/10.1186/s12931-019-1022-1

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