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Results: 1-16 |
Results: 16
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
Authors: HAVERKAMP W HORDT M BREITHARDT G BORGGREFE M
Citation: W. Haverkamp et al., 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, Clinical cardiology, 21(1), 1998, pp. 55-58
KCNE1 MUTATIONS CAUSE JERVELL AND LANGE-NIELSEN-SYNDROME
Authors: SCHULZEBAHR E WANG Q WEDEKIND H HAVERKAMP W CHEN QY SUN YL RUBIE C HORDT M TOWBIN JA BORGGREFE M ASSMANN G QU XD SOMBERG JC BREITHARDT G OBERTI C FUNKE H
Citation: E. Schulzebahr et al., KCNE1 MUTATIONS CAUSE JERVELL AND LANGE-NIELSEN-SYNDROME, Nature genetics, 17(3), 1997, pp. 267-268
AUTOSOMAL RECESSIVE LONG-QT SYNDROME (JERVELL LANGE-NIELSEN SYNDROME)IS GENETICALLY HETEROGENEOUS
Authors: SCHULZEBAHR E HAVERKAMP W WEDEKIND H RUBIE C HORDT M BORGGREFE M ASSMANN G BREITHARDT G FUNKE H
Citation: E. Schulzebahr et al., AUTOSOMAL RECESSIVE LONG-QT SYNDROME (JERVELL LANGE-NIELSEN SYNDROME)IS GENETICALLY HETEROGENEOUS, Human genetics, 100(5-6), 1997, pp. 573-576
IDENTIFICATION OF A NEW GENE FOR AUTOSOMAL RECESSIVE LONG-CT SYNDROME(JERVELL-LANGE-NIELSEN-SYNDROME)
Authors: SCHULZEBAHR E WANG Q HAVERKAMP W WEDEKIND H RUBIE C CHEN QY HORDT M BREITHARDT G FUNKE H
Citation: E. Schulzebahr et al., IDENTIFICATION OF A NEW GENE FOR AUTOSOMAL RECESSIVE LONG-CT SYNDROME(JERVELL-LANGE-NIELSEN-SYNDROME), Circulation, 96(8), 1997, pp. 308-308
DO MUTATIONS IN CARDIAC ION-CHANNEL GENES PREDISPOSE TO DRUG-INDUCED (ACQUIRED) LONG-QT SYNDROME
Authors: SCHULZEBAHR E HAVERKAMP W HORDT M WEDEKIND H BORGGREFE M FUNKE H
Citation: E. Schulzebahr et al., DO MUTATIONS IN CARDIAC ION-CHANNEL GENES PREDISPOSE TO DRUG-INDUCED (ACQUIRED) LONG-QT SYNDROME, Circulation, 96(8), 1997, pp. 1167-1167
GENE WITH GENE INTERACTION INFLUENCES THE EXPRESSIVITY IN CHROMOSOME 11-SPECIFIC (KVLQT1) LONG-QT SYNDROME IN A LARGE GERMAN KINDRED
Authors: WEDEKIND H SCHULZEBAHR E HAVERKAMP W HORDT M LANGE S RUBLE C BORGGREFE M FUNKE H
Citation: H. Wedekind et al., GENE WITH GENE INTERACTION INFLUENCES THE EXPRESSIVITY IN CHROMOSOME 11-SPECIFIC (KVLQT1) LONG-QT SYNDROME IN A LARGE GERMAN KINDRED, Circulation, 96(8), 1997, pp. 1171-1171
IDENTIFICATION AND FUNCTIONAL-CHARACTERIZATION OF A NOVEL GENE FOR AUTOSOMAL RECESSIVE DEAFNESS AND LONG-QT SYNDROME (JERVELL AND LANGE-NIELSEN-SYNDROME)
Authors: SCHULZEBAHR E WANG Q WEDEKIND H HAVERKAMP W CHEN Q SUN Y RUBIE C HORDT M TOWBIN JA BORGGREFE M ASSMANN G QU X SOMBERG JC BREITHARDT G OBERTI C FUNKE H
Citation: E. Schulzebahr et al., IDENTIFICATION AND FUNCTIONAL-CHARACTERIZATION OF A NOVEL GENE FOR AUTOSOMAL RECESSIVE DEAFNESS AND LONG-QT SYNDROME (JERVELL AND LANGE-NIELSEN-SYNDROME), American journal of human genetics, 61(4), 1997, pp. 48-48
A SEVERE FORM OF LONG-QT SYNDROME CAUSED BY 2 KVLQT1 MUTATIONS LOCATED IN CIS
Authors: WEDEKIND H SCHULZEBAHR E LANGE S RUBIE C HAVERKAMP W HORDT M BORGGREFE M ASSMANN G BREITHARDT G FUNKE H
Citation: H. Wedekind et al., A SEVERE FORM OF LONG-QT SYNDROME CAUSED BY 2 KVLQT1 MUTATIONS LOCATED IN CIS, American journal of human genetics, 61(4), 1997, pp. 2051-2051
FREQUENCY AND PHENOTYPE OF HERG MUTATIONS IN CONGENITAL LONG QT SYNDROME (LQTS)
Authors: SCHULZEBAHR E HAVERKAMP W WIEBUSCH H WEDEKIND H HORDT M BORGGREFE M BREITHARDT G FUNKE H
Citation: E. Schulzebahr et al., FREQUENCY AND PHENOTYPE OF HERG MUTATIONS IN CONGENITAL LONG QT SYNDROME (LQTS), Circulation, 94(8), 1996, pp. 4205-4205
MOLECULAR ANALYSIS AT THE HARVEY RAS-1 GENE IN PATIENTS WITH LONG QT SYNDROME
Authors: SCHULZEBAHR E HAVERKAMP W WIEBUSCH H SCHULTE H HORDT M BORGGREFE M BREITHARDT G ASSMANN G FUNKE H
Citation: E. Schulzebahr et al., MOLECULAR ANALYSIS AT THE HARVEY RAS-1 GENE IN PATIENTS WITH LONG QT SYNDROME, Journal of molecular medicine, 73(11), 1995, pp. 565-569
TORSADE-DE-POINTES AND THE QT SYNDROME
Authors: HAVERKAMP W HORDT M BORGGREFE M BREITHARDT G
Citation: W. Haverkamp et al., TORSADE-DE-POINTES AND THE QT SYNDROME, Medizinische Klinik, 90(4), 1995, pp. 240-245
THE IDIOPATHIC LONG QT SYNDROME AS A CAUS E OF EPILEPTIC AND NONEPILEPTIC ATTACKS
Authors: HORDT M HAVERKAMP W OBERWITTLER C LUDEMANN P BORGGREFE M RINGELSTEIN EB BREITHARDT G
Citation: M. Hordt et al., THE IDIOPATHIC LONG QT SYNDROME AS A CAUS E OF EPILEPTIC AND NONEPILEPTIC ATTACKS, Nervenarzt, 66(4), 1995, pp. 282-287
PROARRHYTHMIC EFFECTS OF ANTIARRHYTHMIC D RUGS
Authors: HAVERKAMP W WICHTER T CHEN X HORDT M WILLEMS S ROTMAN B HINDRICKS G KOTTKAMP H BORGGREFE M BREITHARDT G
Citation: W. Haverkamp et al., PROARRHYTHMIC EFFECTS OF ANTIARRHYTHMIC D RUGS, Zeitschrift fur Kardiologie, 83, 1994, pp. 75-85
POLYMORPHIC VENTRICULAR-TACHYCARDIA OR TO RSADE-DE-POINTES
Authors: HAVERKAMP W HORDT M WILLEMS S KOTTKAMP H HINDRICKS G BORGGREFE M BREITHARDT G
Citation: W. Haverkamp et al., POLYMORPHIC VENTRICULAR-TACHYCARDIA OR TO RSADE-DE-POINTES, Herz, Kreislauf, 26(10), 1994, pp. 311-316
TORSADE-DE-POINTES
Authors: HAVERKAMP W HORDT M CHEN X HINDRICKS G WILLEMS S KOTTKAMP H ROTMAN B BRUNN J BORGGREFE M BREITHARDT G
Citation: W. Haverkamp et al., TORSADE-DE-POINTES, Zeitschrift fur Kardiologie, 82(12), 1993, pp. 763-774
TORSADES-DE-POINTES INDUCED BY D,L-SOTALOL
Authors: HAVERKAMP W HORDT M CHEN X WILLEMS S BRUNN J ROTMAN B BORGGREFE M
Citation: W. Haverkamp et al., TORSADES-DE-POINTES INDUCED BY D,L-SOTALOL, Circulation, 88(4), 1993, pp. 397-397
Risultati: 1-16 |