Endothelial Dysfunction in Pulmonary Hypertension: Cause or Consequence?

Pulmonary arterial hypertension (PAH) is a rare, complex, and progressive disease that is characterized by the abnormal remodeling of the pulmonary arteries that leads to right ventricular failure and death. Although our understanding of the causes for abnormal vascular remodeling in PAH is limited,...

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Detalles Bibliográficos
Autores principales: Kurakula, Kondababu, Smolders, Valérie F. E. D., Tura-Ceide, Olga, Jukema, J. Wouter, Quax, Paul H. A., Goumans, Marie-José
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7827874/
https://www.ncbi.nlm.nih.gov/pubmed/33435311
http://dx.doi.org/10.3390/biomedicines9010057

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7827874/
https://www.ncbi.nlm.nih.gov/pubmed/33435311
http://dx.doi.org/10.3390/biomedicines9010057

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