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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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Bibliografski detalji
Glavni autori: Elshaboury, Soha M, Anderson, Joe R
Format: Artigo
Jezik:Inglês
Izdano: Dove Medical Press 2013
Teme:
Online pristup: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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