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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...
Guardat en:
| Publicat a: | Respir Res |
|---|---|
| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2019
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| Matèries: | |
| Accés en línia: | 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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