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- W3118418140 endingPage "177" @default.
- W3118418140 startingPage "167" @default.
- W3118418140 abstract "Pulmonary arterial hypertension (PAH) is a disease of progressive pulmonary vascular remodeling due to abnormal proliferation of pulmonary vascular endothelial and smooth muscle cells and endothelial dysfunction. PAH is a multisystem disease with systemic manifestations and complications. This article covers the chronic heart failure syndrome, including the systemic consequences of right ventricle-pulmonary artery uncoupling and neurohormonal activation, skeletal and respiratory muscle effects, systemic endothelial dysfunction and coronary artery disease, systemic inflammation and infection, endocrine and metabolic changes, the liver and gut axis, sleep, neurologic complications, and skin and iron metabolic changes." @default.
- W3118418140 created "2021-01-18" @default.
- W3118418140 creator A5084534799 @default.
- W3118418140 creator A5091151702 @default.
- W3118418140 creator A5091431458 @default.
- W3118418140 date "2021-03-01" @default.
- W3118418140 modified "2023-09-25" @default.
- W3118418140 title "Pulmonary Vascular Disease as a Systemic and Multisystem Disease" @default.
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- W3118418140 doi "https://doi.org/10.1016/j.ccm.2020.11.001" @default.
- W3118418140 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/33541610" @default.
- W3118418140 hasPublicationYear "2021" @default.