Right Ventricular Adaptation and Failure in Pulmonary Arterial Hypertension

Pulmonary arterial hypertension (PAH) is an obstructive pulmonary vasculopathy, characterized by excess proliferation, apoptosis-resistance, inflammation, fibrosis and vasoconstriction. While PAH therapies target some of these vascular abnormalities (primarily vasoconstriction) most do not directly...

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Publicat a:Can J Cardiol
Autors principals: Ryan, John J., Huston, Jessica, Kutty, Shelby, Hatton, Nathan D., Bowman, Lindsay, Tian, Lian, Herr, Julia E., Johri, Amer M., Archer, Stephen L.
Format: Artigo
Idioma:Inglês
Publicat: 2015
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4385216/
https://ncbi.nlm.nih.gov/pubmed/25840092
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cjca.2015.01.023
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