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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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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Revealing magnetic field structure at the surfaces of protoplanetary disks via near-infrared circular polarization von de Langen, I., Tazaki, R.

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An accurate fatigue damage model for welded joints subjected to variable amplitude loading von Aeran, A, Siriwardane, S C, Mikkelsen, O, Langen, I

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

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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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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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Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases von Charron, Philippe, Arad, Michael, Arbustini, Eloisa, Basso, Cristina, Bilinska, Zofia, Elliott, Perry, Helio, Tiina, Keren, Andre, McKenna, William J., Monserrat, Lorenzo, Pankuweit, Sabine, Perrot, Andreas, Rapezzi, Claudio, Ristic, Arsen, Seggewiss, Hubert, van Langen, Irene, Tavazzi, Luigi

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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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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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A novel susceptibility locus for Hirschsprung’s disease maps to 4q31.3–q32.3 von Brooks, A S, Leegwater, P A, Burzynski, G M, Willems, P J, de Graaf, B, van Langen, I, Heutink, P, Oostra, B A, Hofstra, R M W, Bertoli-Avella, A M

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62. Hypertensive pregnancy disorders: Is the prevalence higher among women with heart disease? von Langen, I., Langesæter, E., Almaas, V., Letting, A., Haugen, G., Estensen, M., Sørbye, I.

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