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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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| Publicado no: | Can J Cardiol |
|---|---|
| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2015
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| Assuntos: | |
| Acesso em linha: | 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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