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...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Pubblicato in:Can J Cardiol
Autori principali: Ryan, John J., Huston, Jessica, Kutty, Shelby, Hatton, Nathan D., Bowman, Lindsay, Tian, Lian, Herr, Julia E., Johri, Amer M., Archer, Stephen L.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2015
Soggetti:
Article
Accesso online: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
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !

Documenti analoghi