Pulmonary Arterial Hypertension: Pathophysiology and Treatment

Pulmonary arterial hypertension (PAH), the first category of pulmonary hypertension, is a chronic and progressive disorder characterised by angioproliferative vasculopathy in the pulmonary arterioles, leading to endothelial and smooth muscle proliferation and dysfunction, inflammation and thrombosis...

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Detalles Bibliográficos
Autores principales: Lan, Norris S. H., Massam, Benjamin D., Kulkarni, Sandeep S., Lang, Chim C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6023499/
https://www.ncbi.nlm.nih.gov/pubmed/29772649
http://dx.doi.org/10.3390/diseases6020038

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6023499/
https://www.ncbi.nlm.nih.gov/pubmed/29772649
http://dx.doi.org/10.3390/diseases6020038

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