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(P1697) |
Hohe Inzidenz von subklinischem Vorhofflimmern bei Patienten mit hypertropher Kardiomyopathie |
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I. K. Wilke, K. Witzel, J. Münch, M. A. Aydin, M. Patten-Hamel (Hamburg) |
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(P1698) |
FHL2 mutations cause hypertrophic cardiomyopathy and induce hypercontractility in engineered heart tissue |
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F. W. Friedrich, S. Reischmann, A. Schwalm, A. Unger, D. P. Ramanujam, J. Münch, O. J. Müller, C. Hengstenberg, E. Galve, P. Charron, W. Linke, S. Engelhardt, M. Patten-Hamel, P. Richard, J. van der Velden, T. Eschenhagen, R. Isnard, L. Carrier (Hamburg, Bochum, München, Heidelberg; Barcelona, ES; Paris, FR; Amsterdam, NL) |
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(P1699) |
Left ventricular hypertrabeculation / noncompaction and pregnancy |
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C. Stöllberger, N. Streit, T. Yoshida, C. Wegner, J. Finsterer (Wien, AT) |
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(P1700) |
Cardiomyopathy in Marfan Syndrome |
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R. Hetzer, P. Gehle, E. M. Delmo-Walter (Berlin) |
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(P1701) |
Left ventricular systolic function – but not the presence of late gadolinium enhancement – independently predicts adverse cardiac events in muscular dystrophy patients |
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A. R. Florian, A. Ludwig, S. Rösch, H. Yildiz, U. Sechtem, A. Yilmaz (Münster, Stuttgart, Kirchheim/Teck) |
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(P1702) |
Cause of cardiac disease in a female carrier of Duchenne Muscular Dystrophy: myocarditis versus genetic cardiomyopathy without skeletal myopathy? |
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A. R. Florian, A. Ludwig, P. Ong, K. Klingel, R. Kandolf, A. Bornemann, U. Sechtem, A. Yilmaz (Münster, Stuttgart, Tübingen) |
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(P1703) |
Understanding the Cardiomyopathy in Friedreich’s Ataxia |
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C. Florescu, M. Niemann, D. Liu, K. Hu, S. Herrmann, P. Gaudron, F. Scholz, S. Störk, G. Ertl, F. Weidemann (Würzburg) |
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(P1704) |
Myocardial fibrosis imaging based on T1-mapping and extracellular volume fraction (ECV) measurement in muscular dystrophy patients: additional diagnostic value compared to conventional LGE |
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A. R. Florian, A. Ludwig, S. Rösch, H. Yildiz, U. Sechtem, A. Yilmaz (Münster, Stuttgart) |
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(P1705) |
Characteristic cardiac phenotypes are detected by cardiovascular magnetic resonance imaging in patients with different clinical phenotypes and genotypes of mitochondrial myopathy |
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A. R. Florian, A. Ludwig, S. Rösch, U. Sechtem, A. Yilmaz (Münster, Stuttgart) |