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Pulmonary Hypertension: Types and Treatments

Pulmonary arterial hypertension (PAH) is a panvasculopathy that affects the distal pulmonary arteries and leads to restricted blood flow. This increased afterload leads to adaptive mechanisms of the right ventricle, with eventual failure once it can no longer compensate. Pulmonary hypertension from...

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Detalhes bibliográficos
Publicado no:Curr Cardiol Rev
Main Authors: Rose-Jones, Lisa J, Mclaughlin, Vallerie V
Formato: Artigo
Idioma:Inglês
Publicado em: Bentham Science Publishers 2015
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4347212/
https://ncbi.nlm.nih.gov/pubmed/24251459
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2174/1573403X09666131117164122
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