Adaptive and innate immune mechanisms in cardiac fibrosis complicating pulmonary arterial hypertension

Pulmonary arterial hypertension (PAH) is a syndrome diagnosed by increased mean pulmonary artery (PA) pressure and resistance and normal pulmonary capillary wedge pressure. PAH is characterized pathologically by distal pulmonary artery remodeling, increased pulmonary vascular resistance, and plexifo...

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Detalles Bibliográficos
Autores principales: Siamwala, Jamila H., Zhao, Alexander, Barthel, Haley, Pagano, Francesco S., Gilbert, Richard J., Rounds, Sharon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Reviews
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7422804/
https://www.ncbi.nlm.nih.gov/pubmed/32786064
http://dx.doi.org/10.14814/phy2.14532

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7422804/
https://www.ncbi.nlm.nih.gov/pubmed/32786064
http://dx.doi.org/10.14814/phy2.14532

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