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- W2058392093 abstract "Einleitung: Pulmonary arterial hypertension (PAH) is a life-threatening disease characterized by increased pulmonary artery pressure, right heart hypertrophy, endothelial injury, proliferation, and hypercontraction of vascular smooth muscle cells (SMCs). COPD frequently complicates its natural evolution with association of PAH. In this context, COPD appears to be complex disease implying pulmonary vascular changes. Endothelial dysfunction has been so far described, but a therapy is not yet in clinical use. Our aim was to investigate the structural changes in the lung vasculature such as muscularization and vascular wall thickening of small pulmonary arteries. Such changes represent hallmarks of PAH." @default.
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- W2058392093 date "2009-02-01" @default.
- W2058392093 modified "2023-10-05" @default.
- W2058392093 title "Morphometric analysis of pulmonary vascular remodeling in COPD" @default.
- W2058392093 doi "https://doi.org/10.1055/s-0029-1202458" @default.
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