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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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| Veröffentlicht in: | Biomedicines |
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| Hauptverfasser: | , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
MDPI
2021
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7827874/ https://ncbi.nlm.nih.gov/pubmed/33435311 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/biomedicines9010057 |
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