Cardiac resynchronization improves microcirculation (2007)
Erol-Yilmaz, A.,
Atasever, B.,
Mathura, K.R.,
Lindeboom, J.A.H.,
Wilde, A.A.M.,
Ince, C.,
...
Cardiac resynchronization improves microcirculation (2007)
Erol-Yilmaz, A.,
Atasever, B.,
Mathura, K.R.,
Lindeboom, J.A.H.,
Wilde, A.A.M.,
Ince, C.,
...
Diurnal variation of ventricular repolarization in a large family with LQT3-Brugada syndrome characterized by nocturnal sudden death (2006)
Haaksma, J.,
Wilde, A.A.M.
BACKGROUND In patients with long-QT syndrome type 3 (LQT3), symptoms occur particularly at rest or during sleep. As to the underlying mechanism, excessive prolongation of the QT interval at slow...
A family with Andersen-Tawil syndrome and dilated cardiomyopathy (2006)
Schoonderwoerd, B.A.,
Wiesfeld, A.C.P.,
Wilde, A.A.M.,
Heuvel, F. Van Den,
Tintelen, J.P. Van,
...
Overlap syndrome of cardiac sodium channel disease in mice carrying the equivalent mutation of human SCN5A-1795insD (2006)
Remme, C.A.,
Verkerk, A.O.,
Nuyens, D.,
Brunschot, S. Van,
Belterman, C.N.W.,
...
Background - Patients carrying the cardiac sodium channel (SCN5A) mutation 1795insD show sudden nocturnal death and signs of multiple arrhythmia syndromes including bradycardia, conduction delay, QT...
Voltage-gated sodium channels: Action players with many faces (2006)
Koopmann, T.T.,
Bezzina, C.R.,
Wilde, A.A.M.
Voltage-gated sodium channels are responsible for the upstroke of the action potential and thereby play an important role in propagation of the electrical impulse in excitable tissues like muscle,...
Female predominance and transmission distortion in the long-QT syndrome (2006)
Imboden, M.,
Swan, H.,
Denjoy, I.,
Langen, I.M. Van,
Latinen-Forsblom, P.J.,
Napolitano, C.,
...
BACKGROUND: Congenital long-QT syndrome is a disorder resulting in ventricular arrhythmias and sudden death. The most common forms of the long-QT syndrome, types 1 and 2, are caused by mutations in...
Structural abnormalities of the inferoseptal left ventricular wall detected by cardiac magnetic resonance imaging in carriers of hypertrophic cardiomyopathy mutations (2006)
Germans, T.,
Wilde, A.A.M.,
Dijkmans, P.A.,
Chai, W.,
Kamp, O.,
Pinto, Y.M.,
...
OBJECTIVES The purpose of this study was to evaluate whether structural left ventricular (LV) abnormalities can be observed in hypertrophic cardiomyopathy (HCM) mutation carriers who have not yet...
Letter regarding article by Darbar et al, "Unmasking of Brugada syndrome by lithium" - Response (2006)
Darbar, D.,
Yang, T.,
Roden, D.M.,
Churchwell, K.,
Wilde, A.A.M.
Letters regarding article by Coronel et al, "Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: A combined electrophysiological, genetic, histopathologic, and computational study" - Response (2006)
Coronel, R.,
Casini, S.,
Koopmann, T.T.,
Verkerk, A.O.,
Groot, J.R. De,
Bezzina, C.R.,
...
Genotype-specific onset of arrhythmias in congenital long-QT syndrome: possible therapy implications (2006)
Tan, H.L.,
Bardai, A.,
Shimizu, W.,
Moss, A.J.,
Schulze-Bahr, E.,
Noda, T.,
...
Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy (2006)
Tintelen, J.P. Van,
Entius, M.M.,
Bhuiyan, Z.A.,
Jongbloed, R.,
Wiesfeld, A.C.P.,
Wilde, A.A.M.,
...
Diagnostic value of flecainide testing in unmasking SCN5A-related Brugada syndrome (2006)
Meregalli, P.G.,
Ruijter, J.M.,
Hofman, N.,
Bezzina, C.R.,
Wilde, A.A.M.,
Tan, H.L.
Familial sudden death is an important risk factor for primary ventricular fibrillation: a case-control study in acute myocardial infarction patients (2006)
Dekker, L.R.C.,
Bezzina, C.R.,
Henriques, J.P.,
Tanck, M.W.T.,
Koch, K.T.,
Alings, M.W.,
...
Common sodium channel promoter haplotype in asian subjects underlies variability in cardiac conduction (2006)
Bezzina, C.R.,
Shimizu, W.,
Yang, P.,
Koopmann, T.T.,
Tanck, M.W.T.,
Miyamoto, Y.,
...
Long QT syndrome caused by a large duplication in the KCNH2 (HERG) gene undetectable by current polymerase chain reaction-based exon-scanning methodologies (2006)
Koopmann, T.T.,
Alders, M.,
Jongbloed, R.J.,
Guerrero, S.,
Wilde, A.A.M.,
...
Preferences of cardiologists and clinical geneticists for the future organization of genetic care in hypertrophic cardiomyopathy: a survey (2005)
Langen, I.M. Van,
Birnie, E.,
Schuurman, E.,
Tan, H.L.,
Hofman, N.,
Bonsel, G.J.,
...
Role of sequence variations in the human ether-a-go-go-related gene (HERG, KCNH2) in the Brugada syndrome (2005)
Verkerk, A.O.,
Wilders, R.,
Schulze-Bahr, E.,
Beekman, L.,
Bhuiyan, Z.A.,
Bertrand, J.,
...
Substitution of a conserved alanine in the domain IIIS4-S5 linker of the cardiac sodium channel causes long QT syndrome (2005)
Smits, J.P.P.,
Veldkamp, M.W.,
Bezzina, C.R.,
Bhuiyan, Z.A.,
Wedekind, H.,
Schulze-Bahr, E.,
...
Can parents adjust to the idea that their child is at risk for a sudden death?: Psychological impact of risk for long QT syndrome (2005)
Grosfeld, F.J.M.,
Tintelen, J.P. Van,
Langen, I.M. Van,
Wilde, A.A.M.,
Bout, J. Van Den,
...
Does flecainide regain its antiarrhythmic activity after electrical cardioversion of persistent atrial fibrillation? (2005)
Tieleman, R.G.,
Gelder, I.C. Van,
Bosker, H.A.,
Kingma, T.,
Wilde, A.A.M.,
...
Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients (2005)
Postma, A.V.,
Denjoy, I.,
Kamblock, J.,
Alders, M.,
Lupoglazoff, J-M.,
Vaksmann, G.,
...
Role of sequence variations in the human ether-a-go-go-related gene (HERG, KCNH2) in the Brugada syndrome (2005)
Verkerk, A.O.,
Wilders, R.,
Schulze-Bahr, E.,
Beekman, L.,
Bhuiyan, Z.A.,
Bertrand, J.,
...
Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: a combined electrophysiological, genetic, histopathologic, and computational study (2005)
Coronel, R.,
Cassini, S.,
Koopmann, T.T.,
Verkerk, A.O.,
Groot, J.R. De,
...
Substitution of a conserved alanine in the domain IIIS4-S5 linker of the cardiac sodium channel causes long QT syndrome (2005)
Smits, J.P.P.,
Veldkamp, M.W.,
Bezzina, C.R.,
Bhuiyan, Z.A.,
Wedekind, H.,
Schulze-Bahr, E.,
...
HERG mutation predicts short QT based on channel kinetics but causes long QT by heterotetrameric trafficking deficiency (2005)
Paulussen, A.D.C.,
Raes, A.,
Jongbloed, R.J.,
Wilde, A.A.M.,
Snyders, D.J.,
...
Preferences of cardiologists and clinical geneticists for the future organization of genetic care in hypertrophic cardiomyopathy: a survey (2005)
Langen, I.M. Van,
Birnie, E.,
Schuurman, E.,
Tan, H.L.,
Hofman, N.,
Bonsel, G.J.,
...
A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families (2005)
Smits, J.P.P.,
Koopmann, T.T.,
Wilders, R.,
Veldkamp, M.W.,
Opthof, T.,
Bhuiyan, Z.A.,
...
Brugada syndrome: report of the second consensus conference (2005)
Antzelevitch, C.,
Brugada, P.,
Borggrefe, M.,
Brugada, J.,
Brugada, R.,
Corrado, D.,
...
Brugada syndrome: report of the second consensus conference (2005)
Antzelevitch, C.,
Brugada, P.,
Borggrefe, M.,
Brugada, J.,
Brugada, R.,
Corrado, D.,
...
Brugada syndrome: overview [ch. 1] (2005)
Antzelevitch, C.,
Brugada, P.,
Borggrefe, M.,
Brugada, J.,
Brugada, R.,
Corrado, D.,
...
A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families (2005)
Smits, J.P.P.,
Koopmann, T.T.,
Wilders, R.,
Veldkamp, M.W.,
Opthof, T.,
Bhuiyan, Z.A.,
...
High distress in parents whose children undergo predictive testing for long QT syndrome (2005)
Grosfeld, F.J.M.,
Wilde, A.A.M.,
Bout, J. Van Den,
Langen, I.M. Van,
Tintelen, J.P. Van,
...