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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Qualitative study of GPs’ views and experiences of population-based preconception expanded carrier screening in the Netherlands: bioethical perspectives von Morberg Jämterud, Sofia, Snoek, Anke, van Langen, I M, Verkerk, Marian, Zeiler, Kristin

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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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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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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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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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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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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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EXTENSION OF THE CLINICAL SPECTRUM OF DANON DISEASE von VAN DER KOOI, A. J, VAN LANGEN, I. M, DE VISSER, M, ARONICA, E, VAN DOOM, P. A, WOKKE, J. H. J, BRUSSE, E, LANGERHORST, C. T, BERGIN, P, DEKKER, L. R. C, DIT DEPREZ, R. H. Lekanne

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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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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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Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system? von Hofman, Nynke, Wilde, Arthur A.M., Kääb, Stefan, van Langen, Irene M., Tanck, Michael W.T., Mannens, Marcel M.A.M., Hinterseer, Martin, Beckmann, Britt-Maria, Tan, Hanno L.

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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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Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands von Christiaans, I., Nannenberg, E. A., Dooijes, D., Jongbloed, R. J. E., Michels, M., Postema, P. G., Majoor-Krakauer, D., van den Wijngaard, A., Mannens, M. M. A. M., van Tintelen, J. P., van Langen, I. M., Wilde, A. A. M.

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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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A Clinical Perspective on Ethical Issues in Genetic Testing von Sijmons, R. H., Van Langen, I. M., Sijmons, J. G.

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Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathy von van Spaendonck-Zwarts, Karin Y, Posafalvi, Anna, van den Berg, Maarten P, Hilfiker-Kleiner, Denise, Bollen, Ilse A E, Sliwa, Karen, Alders, Mariëlle, Almomani, Rowida, van Langen, Irene M, van der Meer, Peter, Sinke, Richard J, van der Velden, Jolanda, Van Veldhuisen, Dirk J, van Tintelen, J Peter, Jongbloed, Jan D H

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Rapid exome sequencing as a first-tier test in neonates with suspected genetic disorder: results of a prospective multicenter clinical utility study in the Netherlands von Olde Keizer, Richelle A. C. M., Marouane, Abderrahim, Kerstjens-Frederikse, Wilhelmina S., Deden, A. Chantal, Lichtenbelt, Klaske D., Jonckers, Tinneke, Vervoorn, Marieke, Vreeburg, Maaike, Henneman, Lidewij, de Vries, Linda S., Sinke, Richard J., Pfundt, Rolph, Stevens, Servi J. C., Andriessen, Peter, van Lingen, Richard A., Nelen, Marcel, Scheffer, Hans, Stemkens, Daphne, Oosterwijk, Cor, van Amstel, Hans Kristian Ploos, de Boode, Willem P., van Zelst-Stams, Wendy A. G., Frederix, Geert W. J., Vissers, Lisenka E. L. 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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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, Jens, van Tintelen, J Peter, Fokstuen, Siv, Elliott, Perry, van Langen, Irene M, Meder, Benjamin, Richard, Pascale, Syrris, Petros, Caforio, Alida L P, Adler, Yehuda, Anastasakis, Aris, Gimeno, Juan R, Klingel, Karin, Linhart, Ales, Imazio, Massimo, Pinto, Yigal, Newbery, Ruth, Schmidtke, Joerg, Charron, Philippe

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