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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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| Publicado no: | Bioelectron Med |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7098229/ https://ncbi.nlm.nih.gov/pubmed/32232109 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s42234-019-0036-9 |
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