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Pulmonary hypertension secondary to pulmonary fibrosis: clinical data, histopathology and molecular insights
Pulmonary hypertension (PH) developing secondarily in pulmonary fibrosis (PF) patients (PF-PH) is a frequent co-morbidity. The high prevalence of PH in PF patients is very concerning since the presence of PH is a strong predictor of mortality in PF patients. Until recently, PH was thought to arise s...
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| Publicado en: | Respir Res |
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| Autores principales: | , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
BioMed Central
2020
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7677848/ https://ncbi.nlm.nih.gov/pubmed/33208169 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12931-020-01570-2 |
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