Diskussionsleiter: R. Schimpf (Mannheim), J. W. Schrickel (Bonn)
(P110) | Predictors of atrial tachyarrhythmias in subjects with type 1 ECG pattern of Brugada syndrome. |
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C. Restle, K. Letsas, R. Weber, J. Stockinger, V.T. Blum, D. Kalusche, T. Arentz (Bad Krozingen) |
(P111) | Prevalence of early repolarization pattern in inferolateral leads in patients with Brugada syndrome |
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K. Astheimer, K. Letsas, R. Weber, D. Kalusche, M. Haissaguerre, T. Arentz (Bad Krozingen; Bordeaux-Pessac, FR) |
(P112) | Brugada like ECG patterns in the German general population |
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M. F. Sinner, A. Pfeufer, S. Perz, E. Schulze-Bahr, G. Mönnig, L. Eckardt, G. Breithardt, G. Steinbeck, H.-E. Wichmann, C. Gieger, T. Meitinger, L. Fabritz, S. Kääb, P. Kirchhof (München, Neuherberg, Münster) |
(P113) | Prevalence of Early Repolarization in the German General Population |
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M. F. Sinner, B. M. Beckmann, W. Reinhard, E. Martens, A. Pfeufer, A. Döring, R. Holle, S. Perz, C. Hengstenberg, S. Kääb (München, Regensburg, Neuherberg) |
(P114) | Genotyp – Phänotyp Korrelation in einer großen kaukasischen Familie mit der E1784K Mutation im SCN5A Gen |
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C. G. Veltmann, G. Strupp, R. Schimpf, C. Antzelevitch, F. Streitner, J. Kuschyk, T. Bonzel, M. Borggrefe, C. Wolpert (Mannheim, Fulda; Utica, US) |
(P115) | Die LQTS-1 assoziierte KCNQ1 Mutation T587M stört die KCNH2 Membranlokalisation und weist einen malignen klinischen Phänotyp auf |
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P. Biliczki, Z. Girmatsion, R. P. Brandes, I. Baro, S. Nattel, S. Hohnloser, J. Ehrlich (Frankfurt am Main; Nantes, FR; Montreal, CA) |
(P116) | Isoproterenol Reduces Dispersion of Cardiac Refractoriness in Transgenic LQT2 Rabbits |
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K. Odening, O. Ziv, B.-R. Choi, G.-X. Liu, M. Kirk, M. Brunner, X. Peng, M. Zehender, G. Koren (Freiburg; Providence, Hershey, US) |
(P117) | More Pronounced Isoproterenol-induced VERP-shortening Due to Increased IKs Current Densities in Female LQT2 Rabbits Account for Steeper QT/RR Ratio in LQT2 Females |
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K. Odening, G.-X. Liu, M. Kirk, M. Brunner, L. Schofield, L. Chaves, X. Peng, M. Zehender, G. Koren (Freiburg; Providence, Hershey, US) |
(P118) | Systematic replication analysis of common genetic variants associated with atrial fibrillation supports two new susceptibility loci |
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M. F. Sinner, A. Pfeufer, B. M. Beckmann, S. Lubitz, S. Perz, C. Gieger, P. T. Ellinor, S. Kääb (München, Neuherberg; Charlestown, US) |
(P119) | Preload-reducing therapy prevents development of ARVC in plakoglobin-deficient mice and preserves connexin expression |
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L. Fabritz, M. Hogendijk, B. P. Sicluna, L. Fortmüller, S. Laakmann, P. Ruiz, H. Witt, T. Wichter, G. Breithardt, J. de Bakker, R. Coronel, P. Kirchhof (Münster, Berlin, Osnabrück; Amsterdam, NL) |
(P120) | Acute inhibition of the Na+/Ca2+ exchanger by SEA0400 reduces proarrhythmia in an experimental model of chronic heart failure |
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P. Milberg, C. Pott, G. Frommeyer, M. Paul, G. Breithardt, L. Eckardt (Münster) |
(P121) | QRS fragmentation in standard ECG as a diagnostic marker of arrhythmogenic right ventricular dysplasia-cardiomyopathy. |
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S. Peters (Goslar) |
(P122) | Suppression of triggered activity underlying antitorsadogenic effects of free polyunsaturated fatty acids in long QT syndrome. |
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P. Milberg, M. Paul, C. Pott, A. Kleideiter, G. Mönnig, G. Breithardt, L. Eckardt (Münster) |