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Molecular mechanisms of right ventricular dysfunction in pulmonary arterial hypertension: focus on the coronary vasculature, sex hormones, and glucose/lipid metabolism

Pulmonary arterial hypertension (PAH) is a rare, life-threatening condition characterized by dysregulated metabolism, pulmonary vascular remodeling, and loss of pulmonary vascular cross-sectional area due to a variety of etiologies. Right ventricular (RV) dysfunction in PAH is a critical mediator of...

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Podrobná bibliografie
Vydáno v:Cardiovasc Diagn Ther
Hlavní autoři: Agrawal, Vineet, Lahm, Tim, Hansmann, Georg, Hemnes, Anna R.
Médium: Artigo
Jazyk:Inglês
Vydáno: AME Publishing Company 2020
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7666935/
https://ncbi.nlm.nih.gov/pubmed/33224772
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/cdt-20-404
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