Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy According to Revised 2010 Task Force Criteria With Inclusion of Non-Desmosomal Phospholamban Mutation Carriers von Groeneweg, Judith A., MD, van der Zwaag, Paul A., MD, PhD, Olde Nordkamp, Louise R.A., MD, Bikker, Hennie, PhD, Jongbloed, Jan D.H., PhD, Jongbloed, Roselie, PhD, Wiesfeld, Ans C.P., MD, PhD, Cox, Moniek G.P.J., MD, PhD, van der Heijden, Jeroen F., MD, PhD, Atsma, Douwe E., MD, PhD, de Boer, Karin, MD, PhD, Doevendans, Pieter A., MD, PhD, Vink, Aryan, MD, PhD, van Veen, Toon A.B., PhD, Dooijes, Dennis, PhD, van den Berg, Maarten P., MD, PhD, Wilde, Arthur A.M., MD, PhD, van Tintelen, J. Peter, MD, PhD, Hauer, Richard N., MD, PhD

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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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Mapping a novel locus for familial atrial fibrillation on chromosome 10p11-q21 von Volders, Paul G.A., MD, PhD, Zhu, Qian, MD, Timmermans, Carl, MD, PhD, Eurlings, Petra M.H., PhD, Su, Xiaoyan, MD, Arens, Yvonne H., MD, PhD, Li, Li, MSc, Jongbloed, Roselie J., PhD, Xia, Min, MD, Rodriguez, Luz-Maria, MD, PhD, Chen, Yi Han, MD, PhD

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Long QT syndrome caused by a large duplication in the KCNH2 (HERG) gene undetectable by current polymerase chain reaction-based exon-scanning methodologies von Koopmann, Tamara T., Alders, Marielle, Jongbloed, Roselie J., Guerrero, Silvia, Mannens, Marcel M.A.M., Wilde, Arthur A.M., Bezzina, Connie R.

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Subepicardial phase 0 block and discontinuous transmural conduction underlie right precordial ST-segment elevation by a SCN5A loss-of-function mutation von Bebarova, Marketa, O'Hara, Tom, Geelen, Jan L. M. C, Jongbloed, Roselie J, Timmermans, Carl, Arens, Yvonne H, Rodriguez, Luz-Maria, Rudy, Yoram, Volders, Paul G. A

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Novel mutation in the per-arnt-sim domain of KCNH2 causes a malignant form of long-QT syndrome von ROSSENBACKER, Tom, MUBAGWA, Kanigula, JONGBLOED, Roselie J, VEREECKE, Johan, DEVRIENDT, Koen, GEWILLIG, Marc, CARMELIET, Edward, COLLEN, Désiré, HEIDBÜCHEL, Hein, CARMELIET, Peter

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Chip-based mtDNA mutation screening enables fast and reliable genetic diagnosis of OXPHOS patients von Van Eijsden, Rudy G.E., Gerards, Mike, Eijssen, Lars M.T., Hendrickx, Alexandra T.M., Jongbloed, Roselie J.E., Wokke, John H.J., Hintzen, Rogier Q., Rubio-Gozalbo, Maria E., De Coo, Irenaeus F.M., Briem, Egill, Tiranti, Valeria, Smeets, Hubert J.M.

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DHPLC analysis of potassium ion channel genes in congenital long QT syndrome von Jongbloed, Roselie, Marcelis, Carlo, Velter, Crool, Doevendans, Pieter, Geraedts, Joep, Smeets, Hubert

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Variable clinical manifestation of a novel missense mutation in the alpha-tropomyosin (TPM1) gene in familial hypertrophic cardiomyopathy von Jongbloed, Roselie J, Marcelis, Carlo L, Doevendans, Pieter A, Schmeitz-Mulkens, Judith M, Van Dockum, Willem G, Geraedts, Joep P, Smeets, Hubert J

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HERG mutation predicts short QT based on channel kinetics but causes long QT by heterotetrameric trafficking deficiency von PAULUSSEN, Aimée D. C, RAES, Adam, JONGBLOED, Roselie J, GILISSEN, Ron A. H. J, WILDE, Arthur A. M, SNYDERS, Dirk J, SMEETS, Hubert J. M, AERSSENS, Jeroen

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A Novel mutation L619F in the cardiac Na+ channel SCN5A associated with long-QT syndrome (LQT3): a role for the I-II linker in inactivation gating von Wehrens, Xander H.T., Rossenbacker, Tom, Jongbloed, Roselie J., Gewillig, Marc, Heidbüchel, Hein, Doevendans, Pieter A., Vos, Marc A., Wellens, Hein J.J., Kass, Robert S.

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Long-QT mutation p.K557E-Kv7.1: dominant-negative suppression of IKs, but preserved cAMP-dependent up-regulation von Spätjens, Roel L.H.M.G., Bébarová, Markéta, Seyen, Sandrine R.M., Lentink, Viola, Jongbloed, Roselie J., Arens, Yvonne H.J.M., Heijman, Jordi, Volders, Paul G.A.

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A genetic variants database for arrhythmogenic right ventricular dysplasia/cardiomyopathy von van der Zwaag, Paul A., Jongbloed, Jan D.H., van den Berg, Maarten P., van der Smagt, Jasper J., Jongbloed, Roselie, Bikker, Hennie, Hofstra, Robert M.W., van Tintelen, J. Peter

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Desmoglein-2 and Desmocollin-2 Mutations in Dutch Arrhythmogenic Right Ventricular Dysplasia/Cardiomypathy Patients: Results From a Multicenter Study von Bhuiyan, Zahurul A, Jongbloed, Jan D.H, van der Smagt, Jasper, Lombardi, Paola M, Wiesfeld, Ans C.P, Nelen, Marcel, Schouten, Meyke, Jongbloed, Roselie, Cox, Moniek G.P.J, van Wolferen, Marleen, Rodriguez, Luz M, van Gelder, Isabelle C, Bikker, Hennie, Suurmeijer, Albert J.H, van den Berg, Maarten P, Mannens, Marcel M.A.M, Hauer, Richard N.W, Wilde, Arthur A.M, van Tintelen, J. Peter

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The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands von Alders, Marielle, Jongbloed, Roselie, Deelen, Wout, van den Wijngaard, Arthur, Doevendans, Pieter, Ten Cate, Folkert, Regitz-Zagrosek, Vera, Vosberg, Hans-Peter, van Langen, Irene, Wilde, Arthur, Dooijes, Dennis, Mannens, Marcel

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The long QT syndrome : a novel missense mutation in the S6 region of the KVLQT1 gene von VAN DEN BERG, M. H, WILDE, A. A. M, ROBLES DE MEDINA, E. O, MEYER, H, GEELEN, J. L. M. C, JONGBLOED, R. J. E, WELLENS, H. J. J, GERAEDTS, J. P. M

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Long-QT mutation p.K557E-Kv7.1: dominant-negative suppression of IKs, but preserved cAMP-dependent up-regulation von Spätjens, Roel L H M G, Bébarová, Markéta, Seyen, Sandrine R M, Lentink, Viola, Jongbloed, Roselie J, Arens, Yvonne H J M, Heijman, Jordi, Volders, Paul G A

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Subepicardial phase 0 block and discontinuous transmural conduction underlie right precordial ST-segment elevation by a SCN5A loss-of-function mutation von BEBAROVA, Markéta, O'HARA, Tom, GEELEN, Jan L. M. C, JONGBLOED, Roselie J, TIMMERMANS, Carl, ARENS, Yvonne H, RODRIGUEZ, Luz-Maria, RUDY, Yoram, VOLDERS, Paul G. A

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RFLP haplotyping and mutation analysis of the phenylalanine hydroxylase gene in Dutch phenylketonuria families von Meijer, H, Jongbloed, R J, Hekking, M, Spaapen, L J, Geraedts, J P

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DHPLC analysis of potassium ion channel genes in congenital long QT syndrome von Jongbloed, Roselie, Marcelis, Carlo, Velter, Crool, Doevendans, Pieter, Geraedts, Joep, Smeets, Hubert

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