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- W2325489898 abstract "Pulmonary arterial hypertension (PAH) is a rare but life-threatening condition that has traditionally required treatment with continuous intravenous epoprostenol via an indwelling central catheter.1–3 Such therapy improves outcome, but is fraught with side effects, expense, and risk of catheter-related complications." @default.
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- W2325489898 date "2007-01-01" @default.
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- W2325489898 title "Pulmonary Arterial Hypertension – Future Directions" @default.
- W2325489898 doi "https://doi.org/10.15420/ecr.2007.0.2.78" @default.
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