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- W2894464379 abstract "Pulmonary arterial hypertension (PAH) is characterised by sustained pulmonary vasoconstriction and remodelling of the pulmonary circulation leading to progressive right ventricular (RV) dysfunction. Although recent registry data suggest improving outcomes, PAH still carries a high morbidity and mortality burden [1]. The risk stratification model from current guidelines accurately predicts survival in scleroderma-associated PAH <http://ow.ly/WmpN30lI5XF>" @default.
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- W2894464379 date "2018-09-27" @default.
- W2894464379 modified "2023-10-18" @default.
- W2894464379 title "Risk assessment in scleroderma patients with newly diagnosed pulmonary arterial hypertension: application of the ESC/ERS risk prediction model" @default.
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- W2894464379 doi "https://doi.org/10.1183/13993003.00497-2018" @default.
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