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M Hördt

Showing results (1-10 of 8) with videos related to

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Clinical Cardiology|February 25, 1998
Torsade de pointes secondary to d,l-sotalol after catheter ablation of incessant atrioventricular reentrant tachycardia--evidence for a significant contribution of the "cardiac memory"W Haverkamp, M Hördt, G Breithardt, et al.
Medizinische Klinik (Munich, Germany : 1983)|April 15, 1995
[Torsade de pointes and QT syndrome]W Haverkamp, M Hördt, M Borggrefe, et al.
Der Nervenarzt|April 1, 1995
[The idiopathic QT syndrome as the cause of epileptic and nonepileptic seizures]M Hördt, W Haverkamp, C Oberwittler, et al.
Zeitschrift Fur Kardiologie|December 1, 1993
[Torsade de pointes]W Haverkamp, M Hördt, X Chen, et al.
Human Genetics|October 28, 1997
Autosomal recessive long-QT syndrome (Jervell Lange-Nielsen syndrome) is genetically heterogeneousE Schulze-Bahr, W Haverkamp, H Wedekind, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 1, 1995
Molecular analysis at the Harvey Ras-1 gene in patients with long QT syndromeE Schulze-Bahr, W Haverkamp, H Wiebusch, et al.
Zeitschrift Fur Kardiologie|January 1, 1994
[The pro-arrhythmic effects of anti-arrhythmia agents]W Haverkamp, T Wichter, X Chen, et al.
Nature Genetics|November 14, 1997
KCNE1 mutations cause jervell and Lange-Nielsen syndromeE Schulze-Bahr, Q Wang, H Wedekind, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Clinical Cardiology|February 25, 1998
Torsade de pointes secondary to d,l-sotalol after catheter ablation of incessant atrioventricular reentrant tachycardia--evidence for a significant contribution of the "cardiac memory"W Haverkamp, M Hördt, G Breithardt, et al.
Medizinische Klinik (Munich, Germany : 1983)|April 15, 1995
[Torsade de pointes and QT syndrome]W Haverkamp, M Hördt, M Borggrefe, et al.
Der Nervenarzt|April 1, 1995
[The idiopathic QT syndrome as the cause of epileptic and nonepileptic seizures]M Hördt, W Haverkamp, C Oberwittler, et al.
Zeitschrift Fur Kardiologie|December 1, 1993
[Torsade de pointes]W Haverkamp, M Hördt, X Chen, et al.
Human Genetics|October 28, 1997
Autosomal recessive long-QT syndrome (Jervell Lange-Nielsen syndrome) is genetically heterogeneousE Schulze-Bahr, W Haverkamp, H Wedekind, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 1, 1995
Molecular analysis at the Harvey Ras-1 gene in patients with long QT syndromeE Schulze-Bahr, W Haverkamp, H Wiebusch, et al.
Zeitschrift Fur Kardiologie|January 1, 1994
[The pro-arrhythmic effects of anti-arrhythmia agents]W Haverkamp, T Wichter, X Chen, et al.
Nature Genetics|November 14, 1997
KCNE1 mutations cause jervell and Lange-Nielsen syndromeE Schulze-Bahr, Q Wang, H Wedekind, et al.
Pageof 1