Potential Molecular Pathways Related to Pulmonary Artery Aneurysm Development: Lessons to Learn from the Aorta

Pulmonary arterial hypertension (PAH) is a rare disease caused by pulmonary vascular remodeling. Current vasodilator treatments have substantially improved patients’ survival. This improved survival has led to the appearance of complications related to conditions previously underdiagnosed or even ig...

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Detalles Bibliográficos
Autores principales: Nuche, Jorge, Palomino-Doza, Julián, Ynsaurriaga, Fernando Arribas, Delgado, Juan F., Ibáñez, Borja, Oliver, Eduardo, Subías, Pilar Escribano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7177585/
https://www.ncbi.nlm.nih.gov/pubmed/32260370
http://dx.doi.org/10.3390/ijms21072509

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7177585/
https://www.ncbi.nlm.nih.gov/pubmed/32260370
http://dx.doi.org/10.3390/ijms21072509

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