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- W2890764600 endingPage "59" @default.
- W2890764600 startingPage "45" @default.
- W2890764600 abstract "Pulmonary arterial hypertension (PAH) is a pulmonary vasculopathy that causes right ventricular dysfunction and exercise limitation and progresses to death. New findings from translational studies have suggested alternative pathways for treatment. These avenues include sex hormones, genetic abnormalities and DNA damage, elastase inhibition, metabolic dysfunction, cellular therapies, and anti-inflammatory approaches. Both novel and repurposed compounds with rationale from preclinical experimental models and human cells are now in clinical trials in patients with PAH. Findings from these studies will elucidate the pathobiology of PAH and may result in clinically important improvements in outcome." @default.
- W2890764600 created "2018-09-27" @default.
- W2890764600 creator A5036938102 @default.
- W2890764600 creator A5060523948 @default.
- W2890764600 creator A5066688315 @default.
- W2890764600 date "2019-01-27" @default.
- W2890764600 modified "2023-10-13" @default.
- W2890764600 title "New and Emerging Therapies for Pulmonary Arterial Hypertension" @default.
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