Molecular Mechanisms of Pulmonary Vascular Remodeling in Pulmonary Arterial Hypertension

Pulmonary arterial hypertension (PAH) is a devastating disease that is precipitated by hypertrophic pulmonary vascular remodeling of distal arterioles to increase pulmonary artery pressure and pulmonary vascular resistance in the absence of left heart, lung parenchymal, or thromboembolic disease. De...

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Detalles Bibliográficos
Autores principales: Leopold, Jane A., Maron, Bradley A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4881582/
https://www.ncbi.nlm.nih.gov/pubmed/27213345
http://dx.doi.org/10.3390/ijms17050761

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4881582/
https://www.ncbi.nlm.nih.gov/pubmed/27213345
http://dx.doi.org/10.3390/ijms17050761

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