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Results: 1-25 | 26-32
Results: 1-25/32
Possible bradycardic mode of death and successful pacemaker treatment in alarge family with features of long QT syndrome type 3 and Brugada syndrome
Authors: van den Berg, MP Wilde, AAM Viersma, JW Brouwer, J Haaksma, J van der Hout, AH Stolte-Dijkstra, I Bezzina, CR van Langen, IM Beaufort-Krol, GCM Cornel, JH Crijns, HJGM
Citation: Mp. Van Den Berg et al., Possible bradycardic mode of death and successful pacemaker treatment in alarge family with features of long QT syndrome type 3 and Brugada syndrome, J CARD ELEC, 12(6), 2001, pp. 630-636
Alterations in potassium channel gene expression in atria of patients withpersistent and paroxysmal atrial fibrillation: Differential regulation of protein and mRNA levels for K+ channels
Authors: Brundel, BJJM Van Gelder, IC Henning, RH Tuinenburg, AE Wietses, M Grandjean, JG Wilde, AAM Van Gilst, WH Crijns, HJGM
Citation: Bjjm. Brundel et al., Alterations in potassium channel gene expression in atria of patients withpersistent and paroxysmal atrial fibrillation: Differential regulation of protein and mRNA levels for K+ channels, J AM COL C, 37(3), 2001, pp. 926-932
Diagnosis and long-term follow-up of the Brugada syndrome in patients withidiopathic ventricular fibrillation
Authors: Remme, CA Wever, EFD Wilde, AAM Derksen, R Hauer, RNW
Citation: Ca. Remme et al., Diagnosis and long-term follow-up of the Brugada syndrome in patients withidiopathic ventricular fibrillation, EUR HEART J, 22(5), 2001, pp. 400-409
K-ATP channel opening during ischemia: Effects on myocardial noradrenalinerelease and ventricular arrhythmias
Authors: Remme, CA Schumacher, CA de Jong, JWJ Fiolet, JWT de Groot, JR Coronel, R Wilde, AAM
Citation: Ca. Remme et al., K-ATP channel opening during ischemia: Effects on myocardial noradrenalinerelease and ventricular arrhythmias, J CARDIO PH, 38(3), 2001, pp. 406-416
Adenosine induced ventricular arrhythmias in the emergency room
Authors: Tan, HL Spekhorst, HHM Peters, RJG Wilde, AAM
Citation: Hl. Tan et al., Adenosine induced ventricular arrhythmias in the emergency room, PACE, 24(4), 2001, pp. 450-455
A sodium-channel mutation causes isolated cardiac conduction disease
Authors: Tan, HL Bink-Boelkens, MTE Bezzina, CR Viswanathan, PC Beaufort-Krol, GCM van Tintelen, PJ van den Berg, MP Wilde, AAM Balser, JR
Citation: Hl. Tan et al., A sodium-channel mutation causes isolated cardiac conduction disease, NATURE, 409(6823), 2001, pp. 1043-1047
Learning from mistakes: The case of clinical electrophysiology - A perspective on evidence-based rhythmology
Authors: Coumel, P Wilde, AAM
Citation: P. Coumel et Aam. Wilde, Learning from mistakes: The case of clinical electrophysiology - A perspective on evidence-based rhythmology, CIRCULATION, 104(7), 2001, pp. 845-847
T-Wave shape in clinical research - Response
Authors: Wilde, AAM Roden, DM
Citation: Aam. Wilde et Dm. Roden, T-Wave shape in clinical research - Response, CIRCULATION, 104(15), 2001, pp. E79-E79
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
Gating-dependent mechanisms for flecainide action in SCN5A-linked arrhythmia syndromes
Authors: Viswanathan, PC Bezzina, CR George, AL Roden, DM Wilde, AAM Balser, JR
Citation: Pc. Viswanathan et al., Gating-dependent mechanisms for flecainide action in SCN5A-linked arrhythmia syndromes, CIRCULATION, 104(10), 2001, pp. 1200-1205
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
LQT genotype-phenotype relationships: patients and patches
Authors: Wilde, AAM Escande, D
Citation: Aam. Wilde et D. Escande, LQT genotype-phenotype relationships: patients and patches, CARDIO RES, 51(4), 2001, pp. 627-629
Cardiac sodium channel and inherited arrhythmia syndromes
Authors: Bezzina, CR Rook, MB Wilde, AAM
Citation: Cr. Bezzina et al., Cardiac sodium channel and inherited arrhythmia syndromes, CARDIO RES, 49(2), 2001, pp. 257-271
K-ATP channel openers, myocardial ischemia, and arrhythmias - Should the electrophysiologist worry?
Authors: Remme, CA Wilde, AAM
Citation: Ca. Remme et Aam. Wilde, K-ATP channel openers, myocardial ischemia, and arrhythmias - Should the electrophysiologist worry?, CARDIO DRUG, 14(1), 2000, pp. 17-22
Genomic organisation and chromosomal localisation of two members of the KCND ion channel family, KCND2 and KCND3
Authors: Postma, AV Bezzina, CR de Vries, JF Wilde, AAM Moorman, AFM Mannens, MMAM
Citation: Av. Postma et al., Genomic organisation and chromosomal localisation of two members of the KCND ion channel family, KCND2 and KCND3, HUM GENET, 106(6), 2000, pp. 614-619
Brugada syndrome and sudden death
Authors: Wilde, AAM Priori, SG
Citation: Aam. Wilde et Sg. Priori, Brugada syndrome and sudden death, EUR HEART J, 21(17), 2000, pp. 1483-1483
Two distinct congenital arrhythmias evoked by a multidysfunctional Na+ channel
Authors: Veldkamp, MW Viswanathan, PC Bezzina, C Baartscheer, A Wilde, AAM Balser, JR
Citation: Mw. Veldkamp et al., Two distinct congenital arrhythmias evoked by a multidysfunctional Na+ channel, CIRCUL RES, 86(9), 2000, pp. E91-E97
Predicting the long-QT genotype from clinical data - From sense to science
Authors: Wilde, AAM Roden, DM
Citation: Aam. Wilde et Dm. Roden, Predicting the long-QT genotype from clinical data - From sense to science, CIRCULATION, 102(23), 2000, pp. 2796-2798
A knockout may not always be a knockout - Response
Authors: Wilde, AAM Mannens, MMAM Alders, M van der Lip, K Hoorntje, TM Sreeram, N van Tintelen, P van der Wal, A
Citation: Aam. Wilde et al., A knockout may not always be a knockout - Response, CIRCULATION, 102(18), 2000, pp. E122-E122
What we can learn from individual resuscitated patients
Authors: Wilde, AAM Veldkamp, MW
Citation: Aam. Wilde et Mw. Veldkamp, What we can learn from individual resuscitated patients, CARDIO RES, 46(1), 2000, pp. 14-16
Cardiac conduction defects associate with mutations in SCN5A
Authors: Schott, JJ Alshinawi, C Kyndt, F Probst, V Hoorntje, TM Hulsbeek, M Wilde, AAM Escande, D Mannens, MMAM Le Marec, H
Citation: Jj. Schott et al., Cardiac conduction defects associate with mutations in SCN5A, NAT GENET, 23(1), 1999, pp. 20-21
Novel KCNQ1 and HERG missense mutations in Dutch long-QT families (vol 13,pg 301, 1998)
Authors: Jongbloed, RJE Wilde, AAM Geelen, JLMC Doevendans, F Schaap, C Van Langen, I van Tintelen, JP Cobben, JM Beaufort-Krol, GCM Geraedts, JPM Smeets, HJM
Citation: Rje. Jongbloed et al., Novel KCNQ1 and HERG missense mutations in Dutch long-QT families (vol 13,pg 301, 1998), HUM MUTAT, 14(1), 1999, pp. 86-86
Novel KCNQ1 and HERG missense mutations in Dutch long-QT families
Authors: Jongbloed, RJE Wilde, AAM Geelen, JLMC Doevendans, P Schaap, C Van Langen, I van Tintelen, JP Cobben, JM Beaufort-Krol, GCM Geraedts, JPM Smeets, HJM
Citation: Rje. Jongbloed et al., Novel KCNQ1 and HERG missense mutations in Dutch long-QT families, HUM MUTAT, 13(4), 1999, pp. 301-310
Drug-induced J point elevation: A marker for genetic risk of sudden death or ECG curiosity?
Authors: Roden, DM Wilde, AAM
Citation: Dm. Roden et Aam. Wilde, Drug-induced J point elevation: A marker for genetic risk of sudden death or ECG curiosity?, J CARD ELEC, 10(2), 1999, pp. 219-223
Long-term (subacute) potassium treatment in congenital HERG-related long QT syndrome (LQTS2)
Authors: Tan, HL Alings, M Van Olden, RW Wilde, AAM
Citation: Hl. Tan et al., Long-term (subacute) potassium treatment in congenital HERG-related long QT syndrome (LQTS2), J CARD ELEC, 10(2), 1999, pp. 229-233
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