Pulmonary arterial hypertension: the case for a bioelectronic treatment

Pulmonary arterial hypertension (PAH) is a rare disease of unknown etiology that progresses to right ventricular failure. It has a complex pathophysiology, which involves an imbalance between vasoconstrictive and vasodilative processes in the pulmonary circulation, pulmonary vasoconstriction, vascul...

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Detalles Bibliográficos
Autores principales: Ntiloudi, Despοina, Qanud, Khaled, Tomaio, Jacquelyn-Nicole, Giannakoulas, George, Al-Abed, Yousef, Zanos, Stavros
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7098229/
https://www.ncbi.nlm.nih.gov/pubmed/32232109
http://dx.doi.org/10.1186/s42234-019-0036-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7098229/
https://www.ncbi.nlm.nih.gov/pubmed/32232109
http://dx.doi.org/10.1186/s42234-019-0036-9

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