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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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.

Volltext

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

Volltext

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

Volltext

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.

Volltext

Novel KCNQ1 and HERG missense mutations in Dutch long‐QT families von Jongbloed, R.J.E., Wilde, A.A.M., Geelen, J.L.M.C., Doevendans, P., Schaap, C., Van Langen, I., van Tintelen, J.P., Cobben, J.M., Beaufort‐Krol, G.C.M., Geraedts, J.P.M., Smeets, H.J.M.

Volltext

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

Volltext

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.

Volltext

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

Volltext

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

Volltext

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

Volltext

The sense and nonsense of direct-to-consumer genetic testing for cardiovascular disease von Janssens, A. C. J. W., Wilde, A. A. M., van Langen, I. M.

Volltext