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Possible value of antifibrotic drugs in patients with progressive fibrosing non-IPF interstitial lung diseases
BACKGROUND: Fibrosing, non-idiopathic pulmonary fibrosis (non-IPF) interstitial lung diseases (fILDs) are a heterogeneous group of diseases characterized by a different amount of inflammation and fibrosis. Therapy is currently based on corticosteroids and/or immunomodulators. However, response to th...
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| Опубликовано в: : | BMC Pulm Med |
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| Главные авторы: | , , , , , , , , , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
BioMed Central
2019
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6852748/ https://ncbi.nlm.nih.gov/pubmed/31718637 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12890-019-0937-0 |
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