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Screening strategies for pulmonary arterial hypertension
Pulmonary arterial hypertension (PAH) is rare and, if untreated, has a median survival of 2–3 years. Pulmonary arterial hypertension may be idiopathic (IPAH) but is frequently associated with other conditions. Despite increased awareness, therapeutic advances, and improved outcomes, the time from sy...
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| Publicado no: | Eur Heart J Suppl |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6915059/ https://ncbi.nlm.nih.gov/pubmed/31857796 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/eurheartj/suz204 |
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