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pro vyhledávání: '"OA Spruijt"'
Autor:
M L Handoko, N Duchateau, I Krstic, S Wahi, C Santoro, M Konopka, S Tuohinen, C Venner, L Spinelli, VJM Baggen, MMP Driessen, MC Post, AP Van Dijk, JW Roos-Hesselink, AE Van Den Bosch, JJM Takkenberg, GT Sieswerda, C A Giudice, D Castaldo, A Pisani, B Trimarco, O Huttin, D Mandry, D Voilliot, JF Chabot, PY Marie, Y Juilliere, A Chaouat, C Selton-Suty, T Skytta, V Virtanen, PL Kellokumpu-Lehtinen, P Raatikainen, K Burkhard-Jagodzinska, W Krol, R Zdanowicz, M Starczewski, K Aniol-Strzyzewska, A Jakubiak, D Sitkowski, M Dluzniewski, W Braksator, A Buonauro, ML Bocchino, R Esposito, A Canora, A Vaccaro, S Castaldo, A Sanduzzi Zamparelli, M Galderisi, A Chong, M Deljanin Ilic, S Vrbic, D Marinkovic, S Ilic, M Sermesant, P Gibelin, E Ferrari, P Moceri, MC Di Pasqua, OA Spruijt, FPT Oosterveer, JT Marcus, HJ Bogaard, A Vonk Noordegraaf
Publikováno v:
European Heart Journal – Cardiovascular Imaging. 16:S67-S69
Purpose: Pulmonary hypertension (PH) is a rare and severe disease for which right ventricular (RV) remodelling and function are associated with survival. The unique anatomy and structure of the RV limit 2D analysis, and its regional function has not