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Ambrisentan for the treatment of pulmonary arterial hypertension: improving outcomes
Pulmonary arterial hypertension (PAH) is a progressive disease of the pulmonary vasculature that is associated with severe functional impairment and a poor prognosis. Ambrisentan is a selective endothelin type A receptor antagonist approved for the treatment of patients with PAH World Health Organiz...
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Dove Medical Press
2013
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3652514/ https://ncbi.nlm.nih.gov/pubmed/23674888 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/PPA.S30949 |
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