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New and Emerging Therapies for Pulmonary Arterial Hypertension
Pulmonary arterial hypertension (PAH) is a pulmonary vasculopathy that causes right ventricular dysfunction and exercise limitation and progresses to death. New findings from translational studies have suggested alternative pathways for treatment. These avenues include sex hormones, genetic abnormal...
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| Опубликовано в: : | Annu Rev Med |
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| Главные авторы: | , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
2018
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7735523/ https://ncbi.nlm.nih.gov/pubmed/30216732 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1146/annurev-med-041717-085955 |
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