Desmin-related myopathy von van Spaendonck-Zwarts, KY, van Hessem, L, Jongbloed, JDH, de Walle, HEK, Capetanaki, Y, van der Kooi, AJ, van Langen, IM, van den Berg, MP, van Tintelen, JP

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Sudden unexplained death : Heritability and diagnostic yield of cardiological and genetic examination in surviving relatives von TAN, Hanno L, HOFMAN, Nynke, VAN LANGEN, Irene M, VAN DER WAL, Allard C, WILDE, Arthur A. M

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Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy von VAN TINTELEN, J. Peter, ENTIUS, Mark M, HOFSTRA, Robert M. W, OTTERSPOOR, Luuk C, DOEVENDANS, Pieter A. F. M, RODRIGUEZ, Luz-Maria, VAN GELDER, Isabelle C, HAUER, Richard N. W, BHUIYAN, Zahurul A, JONGBLOED, Roselie, WIESFELD, Ans C. P, WILDE, Arthur A. M, VAN DER SMAGT, Jasper, BOVEN, Ludolf G, MANNENS, Marcel M. A. M, VAN LANGEN, Irene M

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A Single Na+ Channel Mutation Causing Both Long-QT and Brugada Syndromes von Bezzina, Connie, Veldkamp, Marieke W, van den Berg, Maarten P, Postma, Alex V, Rook, Martin B, Viersma, Jan-Willem, van Langen, Irene M, Tan-Sindhunata, Ghita, Bink-Boelkens, Margreet Th. E, van der Hout, Annemarie H, Mannens, Marcel M. A. M, Wilde, Arthur A. M

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A Cardiac Sodium Channel Mutation Cosegregates With a Rare Connexin40 Genotype in Familial Atrial Standstill von Groenewegen, W Antoinette, Firouzi, Mehran, Bezzina, Connie R, Vliex, Saskia, van Langen, Irene M, Sandkuijl, Lodewijk, Smits, Jeroen P.P, Hulsbeek, Miriam, Rook, Martin B, Jongsma, Habo J, Wilde, Arthur A.M

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Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1) von Wilde, Arthur A.M, Jongbloed, Rosalie J.E, Doevendans, Pieter A, Düren, Donald R, Hauer, Richard N.W, van Langen, Irene M, van Tintelen, J.Peter, Smeets, Hubert J.M, Meyer, Henk, Geelen, Jan L.M.C

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Haplotype sharing test maps genes for familial cardiomyopathies von van der Zwaag, PA, van Tintelen, JP, Gerbens, F, Jongbloed, JDH, Boven, LG, van der Smagt, JJ, van der Roest, WP, van Langen, IM, Bikker, H, Hauer, RNW, van den Berg, MP, Hofstra, RMW, te Meerman, GJ

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The use of genotype-phenotype correlations in mutation analysis for the long QT syndrome von Van Langen, I M, Birnie, E, Alders, M, Jongbloed, R J, Le Marec, H, Wilde, A A M

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Possible Bradycardic Mode of Death and Successful Pacemaker Treatment in a Large Family with Features of Long QT Syndrome Type 3 and Brugada Syndrome von VAN DEN BERG, MAARTEN P., WILDE, ARTHUR A.M., VIERSMA, JAN WILLEM, BROUWER, JAN, HAAKSMA, JAAP, VAN DER HOUT, ANNEMIEKE H., STOLTE-DIJKSTRA, IRENE, BEZZINA, CONNIE R., VAN LANGEN, IRENE M., BEAUFORT-KROL, GERTIE C.M., CORNEL, JAN HEIN, CRIJNS, HARRY J.G.M.

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Can parents adjust to the idea that their child is at risk for a sudden death?: Psychological impact of risk for long QT syndrome von Hendriks, Karin S.W.H., Grosfeld, F.J.M., van Tintelen, J.P., van Langen, I.M., Wilde, A.A.M., van den Bout, J., ten Kroode, H.F.J.

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Genetic knowledge and counselling skills of Dutch cardiologists: sufficient for the genomics era? von van Langen, I.M, Birnie, E, Leschot, N.J, Bonsel, G.J, Wilde, A.A.M

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Family and population strategies for screening and counselling of inherited cardiac arrhythmias von van Langen, I M, Hofman, N, Tan, H L, Wilde, A A M

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Preferences of cardiologists and clinical geneticists for the future organization of genetic care in hypertrophic cardiomyopathy: a survey von Van Langen, IM, Birnie, E, Schuurman, E, Tan, HL, Hofman, N, Bonsel, GJ, Wilde, AAM

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High Distress in Parents Whose Children Undergo Predictive Testing for Long QT Syndrome von Hendriks, Karin S.W.H., Grosfeld, F.J.M., Wilde, A.A.M., van den Bout, J., van Langen, I.M., van Tintelen, J.P., Kroode, H.F.J. ten

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Gender differences in the long QT syndrome: effects of β-adrenoceptor blockade von CONRATH, Chantal E, WILDE, Arthur A. M, JONGBLOED, Rosalie J. E, ALDERS, Mariëlle, VAN LANGEN, Irene M, VAN TINTELEN, J. Peter, DOEVENDANS, Pieter A, OPTHOF, Tobias

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A new mutation in the prion protein gene : A patient with dementia and white matter changes von VAN HARTEN, B, VAN GOOL, W. A, VAN LANGEN, I. M, DEEKMAN, J. M, MEIJERINK, P. H. S, WEINSTEIN, H. C

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Short Report: Preferences of cardiologists and clinical geneticists for the future organization of genetic care in hypertrophic cardiomyopathy: a survey von IM van Langen, Birnie, E, Schuurman, E, Tan, H L, Hofman, N, Bonsel, G J, Wilde, AAM

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The current role of next-generation DNA sequencing in routine care of patients with hereditary cardiovascular conditions: a viewpoint paper of the European Society of Cardiology wo... von Mogensen, J, van Tintelen, JP, Fokstuen, S, Elliott, P, van Langen, IM, Meder, B, Richard, P, Syrris, P, Caforio, ALP, Adler, Y, Anastasakis, A, Gimeno, JR, Klingel, K, Linhart, A, Imazio, M, Pinto, Y, Newbery, R, Schmidtke, J, Charron, P

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Polytopic anomalies with agenesis of the lower vertebral column von Bohring, Axel, Lewin, Susan O., Reynolds, James F., Voigtländer, Theda, Rittinger, Olaf, Carey, John C., Köpernik, Michael, Smith, Rosemarie, Zackai, Elaine H., Leonard, Norma J., Gritter, Hilda L., Bamforth, J. Stephen, Okun, Nannette, McLeod, D. Ross, Super, Maurice, Powell, Peter, Mundlos, Stefan, Hennekam, Raoul C.M., van Langen, Irene M., Viskochil, David H., Wiedemann, Hans-Rudolf, Opitz, John M.

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A gene for autosomal recessive nemaline myopathy assigned to chromosome 2q by linkage analysis von Wallgren-Pettersson, C., Avela, K., Marchand, S., Kolehmainen, J., Tahvanainen, E., Hansen, F.Juul, Muntoni, F., Dubowitz, V., de Visser, M., van Langen, I.M., Laing, Nigel G., Fauré, S., de la Chapelle, A.

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