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Results: 1-20 |
Results: 20
Genetic aspects in acquired long QT syndrome - a piece in the puzzle
Authors: Schulze-Bahr, E Haverkamp, W Eckardt, L Kirchhof, P Wedekind, H Breithardt, G
Citation: E. Schulze-bahr et al., Genetic aspects in acquired long QT syndrome - a piece in the puzzle, EUR H J SUP, 3(K), 2001, pp. K48-K52
Clinical aspects of ventricular arrhythmias associated with QT prolongation
Authors: Haverkamp, W Eckardt, L Monnig, G Schulze-Bahr, E Wedekind, H Kirchhof, P Haverkamp, F Breithardt, G
Citation: W. Haverkamp et al., Clinical aspects of ventricular arrhythmias associated with QT prolongation, EUR H J SUP, 3(K), 2001, pp. K81-K88
Brugada syndrome and supraventricular tachyarrhythmias: A novel association?
Authors: Eckardt, L Kirchhof, P Loh, P Schulze-Bahr, E Johna, R Wichter, T Breithardt, G Haverkamp, W Borggrefe, M
Citation: L. Eckardt et al., Brugada syndrome and supraventricular tachyarrhythmias: A novel association?, J CARD ELEC, 12(6), 2001, pp. 680-685
A novel long-QT 5 gene mutation in the C-terminus (V1091) is associated with a mild phenotype
Authors: Schulze-Bahr, E Schwarz, M Hoffmann, S Wedekind, H Funke, H Haverkamp, W Breithardt, G Pongs, O Isbrandt, D
Citation: E. Schulze-bahr et al., A novel long-QT 5 gene mutation in the C-terminus (V1091) is associated with a mild phenotype, J MOL MED-J, 79(9), 2001, pp. 504-509
Clinical value of electrocardiographic parameters in genotyped individualswith familial long QT syndrome
Authors: Moennig, G Schulze-Bahr, E Wedekind, H Borggrefe, M Funke, H Toelle, M Kirchhof, P Eckardt, L Assmann, G Breithardt, G Haverkamp, W
Citation: G. Moennig et al., Clinical value of electrocardiographic parameters in genotyped individualswith familial long QT syndrome, PACE, 24(4), 2001, pp. 406-415
Molecular diagnosis in a child with sudden infant death syndrome
Authors: Schwartz, PJ Priori, SG Bloise, R Napolitano, C Ronchetti, E Piccinini, A Goj, C Breithardt, G Schulze-Bahr, E Wedekind, H Nastoli, J
Citation: Pj. Schwartz et al., Molecular diagnosis in a child with sudden infant death syndrome, LANCET, 358(9290), 2001, pp. 1342-1343
De novo mutation in the SCN5A gene associated with early onset of sudden infant death
Authors: Wedekind, H Smits, JPP Schulze-Bahr, E Arnold, R Veldkamp, MW Bajanowski, T Borggrefe, M Brinkmann, B Warnecke, I Funke, H Bhuiyan, ZA Wilde, AAM Breithardt, G Haverkamp, W
Citation: H. Wedekind et al., De novo mutation in the SCN5A gene associated with early onset of sudden infant death, CIRCULATION, 104(10), 2001, pp. 1158-1164
Genotype-phenotype correlation in the long-QT syndrome - Gene-specific triggers for life-threatening arrhythmias
Authors: Schwartz, PJ Priori, SG Spazzolini, C Moss, AJ Vincent, GM Napolitano, C Denjoy, I Guicheney, P Breithardt, G Keating, MT Towbin, JA Beggs, AH Brink, P Wilde, AAM Toivonen, L Zareba, W Robinson, JL Timothy, KW Corfield, V Wattanasirichaigoon, D Corbett, C Haverkamp, W Schulze-Bahr, E Lehmann, MH Schwartz, K Coumel, P Bloise, R
Citation: Pj. Schwartz et al., Genotype-phenotype correlation in the long-QT syndrome - Gene-specific triggers for life-threatening arrhythmias, CIRCULATION, 103(1), 2001, pp. 89-95
Mechanisms and clinical aspects of ventricular arrhythmias associated withQT prolongation: Torsades de pointes
Authors: Haverkamp, W Monnig, G Eckardt, L Kirchhof, PF Schulze-Bahr, E Wedekind, H Haverkamp, F Borggrefe, M Breithardt, G
Citation: W. Haverkamp et al., Mechanisms and clinical aspects of ventricular arrhythmias associated withQT prolongation: Torsades de pointes, MYOCARDIAL REPOLARIZATION: FROM GENE TO BEDSIDE, 2001, pp. 151-169
Sudden infant death syndrome: Is there a genetic basis?
Authors: Wedekind, H Schulze-Bahr, E Haverkamp, W Bajanowski, T Brinkmann, MB Breithardt, G
Citation: H. Wedekind et al., Sudden infant death syndrome: Is there a genetic basis?, MYOCARDIAL REPOLARIZATION: FROM GENE TO BEDSIDE, 2001, pp. 279-289
Genetic aspects in acquired long QT syndrome
Authors: Schulze-Bahr, E Denjoy, I Haverkamp, W Breithardt, G Guicheney, P
Citation: E. Schulze-bahr et al., Genetic aspects in acquired long QT syndrome, MYOCARDIAL REPOLARIZATION: FROM GENE TO BEDSIDE, 2001, pp. 333-341
How to avoid drug-induced - Torsades de pointes
Authors: Breithardt, G Borggrefe, M Schulze-Bahr, E Haverkamp, W
Citation: G. Breithardt et al., How to avoid drug-induced - Torsades de pointes, MYOCARDIAL REPOLARIZATION: FROM GENE TO BEDSIDE, 2001, pp. 353-361
A patient with "atrial torsades de pointes"
Authors: Kirchhof, P Eckardt, L Monnig, G Johna, R Loh, P Schulze-Bahr, E Breithardt, G Borggrefe, M Haverkamp, W
Citation: P. Kirchhof et al., A patient with "atrial torsades de pointes", J CARD ELEC, 11(7), 2000, pp. 806-811
Molecular genetics of arrhythmias - a new paradigm
Authors: Schulze-Bahr, E Haverkamp, W Borggrefe, M Wedekind, H Monnig, G Mergenthaler, J Assmann, G Funke, H Breithardt, G
Citation: E. Schulze-bahr et al., Molecular genetics of arrhythmias - a new paradigm, Z KARDIOL, 89, 2000, pp. 12-22
New aspects in cardiac arrhythmias: the roll of ion channels and genetic aspects
Authors: Haverkamp, W Eckardt, L Kirchhof, P Monnig, G Schulze-Bahr, E Wedekind, H Borggrefe, M Madeja, M Breithardt, G
Citation: W. Haverkamp et al., New aspects in cardiac arrhythmias: the roll of ion channels and genetic aspects, Z KARDIOL, 89, 2000, pp. 2-9
Clinical aspects and molecular genetics of the long Q-T syndrome
Authors: Haverkamp, W Monnig, G Wedekind, H Schulze-Bahr, E Borggrefe, M Assmann, G Funke, H Breithardt, G
Citation: W. Haverkamp et al., Clinical aspects and molecular genetics of the long Q-T syndrome, DEUT MED WO, 124(33), 1999, pp. 972-979
Multistep-touchdown vectorette-PCR - A rapid technique for the identification of IVS in genes
Authors: Rubie, C Schulze-Bahr, E Wedekind, H Borggrefe, M Haverkamp, W Breithardt, G
Citation: C. Rubie et al., Multistep-touchdown vectorette-PCR - A rapid technique for the identification of IVS in genes, BIOTECHNIQU, 27(3), 1999, pp. 414
The LQT syndromes - current status of molecular mechanisms
Authors: Schulze-Bahr, E Wedekind, H Haverkamp, W Borggrefe, M Assmann, G Breithardt, G Funke, H
Citation: E. Schulze-bahr et al., The LQT syndromes - current status of molecular mechanisms, Z KARDIOL, 88(4), 1999, pp. 245-254
C-terminal HERG mutations - The role of hypokalemia and a KCNQ1-associatedmutation in cardiac event occurrence
Authors: Berthet, M Denjoy, I Donger, C Demay, L Hammoude, H Klug, D Schulze-Bahr, E Richard, P Funke, H Schwartz, K Coumel, P Hainque, B Guicheney, P
Citation: M. Berthet et al., C-terminal HERG mutations - The role of hypokalemia and a KCNQ1-associatedmutation in cardiac event occurrence, CIRCULATION, 99(11), 1999, pp. 1464-1470
Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndrome
Authors: Chen, QY Zhang, DM Gingell, RL Moss, AJ Napolitano, C Priori, SG Schwartz, PJ Kehoe, E Robinson, JL Schulze-Bahr, E Wang, Q Towbin, JA
Citation: Qy. Chen et al., Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndrome, CIRCULATION, 99(10), 1999, pp. 1344-1347
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