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Autor:
Brett E. Fenster, Benjamin S. Frank, Lexie K. Ross, Max B. Mitchell, Michal Shafer, D. Dunbar Ivy, Kendall S. Hunter, Alex J. Barker, Gareth J. Morgan
Publikováno v:
Circulation. 142
Introduction: Idiopathic Pulmonary Arterial Hypertension (PH-Type I) and PH due to pulmonary disease (PH-Type III) arise from different pathophysiologic processes, yet they both culminate in increased right ventricular (RV) afterload and eventual RV