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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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| 出版年: | Annu Rev Med |
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| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2018
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| 主題: | |
| オンライン･アクセス: | 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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