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Ambrisentan: a review of its use in pulmonary arterial hypertension

Pulmonary arterial hypertension (PAH) is a progressive disease defined by an elevation in pulmonary arterial pressure that can lead to right heart failure and death. Ambrisentan is a selective endothelin receptor antagonist approved for the treatment of idiopathic, heritable PAH and connective tissu...

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Detalhes bibliográficos
Publicado no:Ther Adv Respir Dis
Main Authors: Rivera-Lebron, Belinda N., Risbano, Michael G.
Formato: Artigo
Idioma:Inglês
Publicado em: SAGE Publications 2017
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5933647/
https://ncbi.nlm.nih.gov/pubmed/28425346
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1753465817696040
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