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Antifibrotic therapy for idiopathic pulmonary fibrosis: time to treat
Idiopathic pulmonary fibrosis (IPF) is a progressive disease with a dismal prognosis. The average life expectancy of untreated patients with IPF is only 3 to 4 years. Decline in forced vital capacity (FVC) in patients with IPF appears to be almost linear, with patients with well-preserved FVC at bas...
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| Publicado no: | Respir Res |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6731623/ https://ncbi.nlm.nih.gov/pubmed/31492155 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12931-019-1161-4 |
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