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The molecular targets of approved treatments for pulmonary arterial hypertension

Until recently, three classes of medical therapy were available for the treatment of pulmonary arterial hypertension (PAH)—prostanoids, endothelin receptor antagonists and phosphodiesterase type 5 (PDE5) inhibitors. With the approval of the soluble guanylate cyclase stimulator riociguat, an addition...

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Bibliografski detalji
Izdano u:Thorax
Glavni autori: Humbert, Marc, Ghofrani, Hossein-Ardeschir
Format: Artigo
Jezik:Inglês
Izdano: BMJ Publishing Group 2016
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4717417/
https://ncbi.nlm.nih.gov/pubmed/26219978
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/thoraxjnl-2015-207170
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