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Neprilysin inhibition for pulmonary arterial hypertension: a randomized, double‐blind, placebo‐controlled, proof‐of‐concept trial

BACKGROUND AND PURPOSE: Pulmonary arterial hypertension (PAH) is an incurable, incapacitating disorder resulting from increased pulmonary vascular resistance, pulmonary arterial remodelling, and right ventricular failure. In preclinical models, the combination of a PDE5 inhibitor (PDE5i) with a nepr...

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Detalles Bibliográficos
Publicado en:Br J Pharmacol
Autores principales: Hobbs, Adrian J., Moyes, Amie J., Baliga, Reshma S., Ghedia, Dipa, Ochiel, Rachel, Sylvestre, Yvonne, Doré, Caroline J., Chowdhury, Kashfia, Maclagan, Kate, Quartly, Harriet L., Sofat, Reecha, Smit, Angelique, Schreiber, Benjamin E., Coghlan, Gerry J., MacAllister, Raymond J.
Formato: Artigo
Lenguaje:Inglês
Publicado: John Wiley and Sons Inc. 2019
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC7651846/
https://ncbi.nlm.nih.gov/pubmed/30761523
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bph.14621
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