Isolated Subepicardial Right Ventricular Outflow Tract Scar in Athletes With Ventricular Tachycardia von Venlet, Jeroen, MD, Piers, Sebastiaan R.D., MD, PhD, Jongbloed, Jan D.H., PhD, Androulakis, Alexander F.A., MD, Naruse, Yoshihisa, MD, PhD, den Uijl, Dennis W., MD, PhD, Kapel, Gijsbert F.L., MD, de Riva, Marta, MD, van Tintelen, J. Peter, MD, PhD, Barge-Schaapveld, Daniela Q.C.M., MD, PhD, Schalij, Martin J., MD, PhD, Zeppenfeld, Katja, MD, PhD

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Reduced kinase function in two ultra‐rare TNNI3K variants in families with congenital junctional ectopic tachycardia von Pham, Caroline, Koopmann, Tamara T., Vinocur, Jeffrey M., Blom, Nico A., Nogueira Silbiger, Vivian, Mittal, Kirti, Bootsma, Marianne, Palm, Kaylin C. A., Clur, Sally‐Ann B., Barge‐Schaapveld, Daniela Q. C. M., Hamilton, Robert M., Lodder, Elisabeth M.

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A mutation update for the FLNC gene in myopathies and cardiomyopathies von Verdonschot, Job A. J., Vanhoutte, Els K., Claes, Godelieve R. F., Helderman‐van den Enden, Apollonia T. J. M., Hoeijmakers, Janneke G. J., Hellebrekers, Debby M. E. I., Haan, Amber, Christiaans, Imke, Lekanne Deprez, Ronald H., Boen, Hanne M., Craenenbroeck, Emeline M., Loeys, Bart L., Hoedemaekers, Yvonne M., Marcelis, Carlo, Kempers, Marlies, Brusse, Esther, Waning, Jaap I., Baas, Annette F., Dooijes, Dennis, Asselbergs, Folkert W., Barge‐Schaapveld, Daniela Q. C. M., Koopman, Pieter, Wijngaard, Arthur, Heymans, Stephane R. B., Krapels, Ingrid P. C., Brunner, Han G.

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Germline variant affecting p53β isoforms predisposes to familial cancer von Schubert, Stephanie A., Ruano, Dina, Joruiz, Sebastien M., Stroosma, Jordy, Glavak, Nikolina, Montali, Anna, Pinto, Lia M., Rodríguez-Girondo, Mar, Barge-Schaapveld, Daniela Q. C. M., Nielsen, Maartje, van Nesselrooij, Bernadette P. M., Mensenkamp, Arjen R., van Leerdam, Monique E., Sharp, Thomas H., Morreau, Hans, Bourdon, Jean-Christophe, de Miranda, Noel F. C. C., van Wezel, Tom

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Toward an effective exome-based genetic testing strategy in pediatric dilated cardiomyopathy von Herkert, Johanna C, Abbott, Kristin M, Birnie, Erwin, Meems-Veldhuis, Martine T, Boven, Ludolf G, Benjamins, Marloes, du Marchie Sarvaas, Gideon J, Barge-Schaapveld, Daniela Q C M, van Tintelen, J Peter, van der Zwaag, Paul A, Vos, Yvonne J, Sinke, Richard J, van den Berg, Maarten P, van Langen, Irene M, Jongbloed, Jan D H

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GATA6 mutations: Characterization of two novel patients and a comprehensive overview of the GATA6 genotypic and phenotypic spectrum von Škorić‐Milosavljević, Doris, Tjong, Fleur V. Y., Barc, Julien, Backx, Ad P. C. M., Clur, Sally‐Ann B., Spaendonck‐Zwarts, Karin, Oostra, Roelof‐Jan, Lahrouchi, Najim, Beekman, Leander, Bökenkamp, Regina, Barge‐Schaapveld, Daniela Q. C. M., Mulder, Barbara J., Lodder, Elisabeth M., Bezzina, Connie R., Postma, Alex V.

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Expanding the clinical and genetic spectrum of ALPK3 variants: Phenotypes identified in pediatric cardiomyopathy patients and adults with heterozygous variants von Herkert, Johanna C., Verhagen, Judith M.A., Yotti, Raquel, Haghighi, Alireza, Phelan, Dean G., James, Paul A., Brown, Natasha J., Stutterd, Chloe, Macciocca, Ivan, Leong, Kai'En, Bulthuis, Marian L.C., van Bever, Yolande, van Slegtenhorst, Marjon A., Boven, Ludolf G., Roberts, Amy E., Agarwal, Radhika, Seidman, Jonathan, Lakdawala, Neal K., Fernández-Avilés, Francisco, Burke, Michael A., Pierpont, Mary Ella, Braunlin, Elizabeth, Ḉağlayan, Ahmet Okay, Barge-Schaapveld, Daniela Q.C.M., Birnie, Erwin, van Osch-Gevers, Lennie, van Langen, Irene M., Jongbloed, Jan D.H., Lockhart, Paul J., Amor, David J., Seidman, Christine E., van de Laar, Ingrid M.B.H.

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Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome von Weerts, Marjolein J. A., Lanko, Kristina, Guzmán-Vega, Francisco J., Jackson, Adam, Ramakrishnan, Reshmi, Cardona-Londoño, Kelly J., Peña-Guerra, Karla A., van Bever, Yolande, van Paassen, Barbara W., Kievit, Anneke, van Slegtenhorst, Marjon, Allen, Nicholas M., Kehoe, Caroline M., Robinson, Hannah K., Pang, Lewis, Banu, Selina H., Zaman, Mashaya, Efthymiou, Stephanie, Houlden, Henry, Järvelä, Irma, Lauronen, Leena, Määttä, Tuomo, Schrauwen, Isabelle, Leal, Suzanne M., Ruivenkamp, Claudia A. L., Barge-Schaapveld, Daniela Q.C.M., Peeters-Scholte, Cacha M. P. C. D., Galehdari, Hamid, Mazaheri, Neda, Sisodiya, Sanjay M., Harrison, Victoria, Sun, Angela, Thies, Jenny, Pedroza, Luis Alberto, Lara-Taranchenko, Yana, Chinn, Ivan K., Lupski, James R., Garza-Flores, Alexandra, McGlothlin, Jeffery, Yang, Lin, Huang, Shaoping, Wang, Xiaodong, Jewett, Tamison, Rosso, Gretchen, Lin, Xi, Mohammed, Shehla, Merritt, J. Lawrence, Mirzaa, Ghayda M., Timms, Andrew E., Scheck, Joshua, Elting, Mariet W., Polstra, Abeltje M., Schenck, Lauren, Ruzhnikov, Maura R. Z., Vetro, Annalisa, Montomoli, Martino, Guerrini, Renzo, Koboldt, Daniel C., Mosher, Theresa Mihalic, Pastore, Matthew T., McBride, Kim L., Peng, Jing, Pan, Zou, Willemsen, Marjolein, Koning, Susanne, Turnpenny, Peter D., de Vries, Bert B. A., Gilissen, Christian, Pfundt, Rolph, Lees, Melissa, Braddock, Stephen R., Klemp, Kara C., Vansenne, Fleur, van Gijn, Marielle E., Quindipan, Catherine, Deardorff, Matthew A., Hamm, J. Austin, Putnam, Abbey M., Baud, Rebecca, Walsh, Laurence, Lynch, Sally A., Baptista, Julia, Person, Richard E., Monaghan, Kristin G., Crunk, Amy, Keller-Ramey, Jennifer, Reich, Adi, Elloumi, Houda Zghal, Alders, Marielle, Kerkhof, Jennifer, McConkey, Haley, Haghshenas, Sadegheh, Maroofian, Reza, Sadikovic, Bekim, Banka, Siddharth, Arold, Stefan T., Barakat, Tahsin Stefan

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The atypical 16p11.2 deletion: A not so atypical microdeletion syndrome? von Barge-Schaapveld, Daniela Q.C.M., Maas, Saskia M., Polstra, Abeltje, Knegt, Lia C., Hennekam, Raoul C.M.

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Characterization of Degenerative Mitral Valve Disease: Differences between Fibroelastic Deficiency and Barlow's Disease von van Wijngaarden, Aniek L, Kruithof, Boudewijn P T, Vinella, Tommaso, Barge-Schaapveld, Daniela Q C M, Ajmone Marsan, Nina

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Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders von Stolz, Jacob R., Foote, Kendall M., Veenstra-Knol, Hermine E., Pfundt, Rolph, ten Broeke, Sanne W., de Leeuw, Nicole, Roht, Laura, Pajusalu, Sander, Part, Reelika, Rebane, Ionella, Õunap, Katrin, Stark, Zornitza, Kirk, Edwin P., Lawson, John A., Lunke, Sebastian, Christodoulou, John, Louie, Raymond J., Rogers, R. Curtis, Davis, Jessica M., Innes, A. Micheil, Wei, Xing-Chang, Keren, Boris, Mignot, Cyril, Lebel, Robert Roger, Sperber, Steven M., Sakonju, Ai, Dosa, Nienke, Barge-Schaapveld, Daniela Q.C.M., Peeters-Scholte, Cacha M.P.C.D., Ruivenkamp, Claudia A.L., van Bon, Bregje W., Kennedy, Joanna, Low, Karen J., Ellard, Sian, Pang, Lewis, Junewick, Joseph J., Mark, Paul R., Carvill, Gemma L., Swanson, Geoffrey T.

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Reclassification of a likely pathogenic Dutch founder variant in KCNH2; implications of reduced penetrance von Copier, Jaël S, Bootsma, Marianne, Ng, Chai A, Wilde, Arthur A M, Bertels, Robin A, Bikker, Hennie, Christiaans, Imke, van der Crabben, Saskia N, Hol, Janna A, Koopmann, Tamara T, Knijnenburg, Jeroen, Lommerse, Aafke A J, van der Smagt, Jasper J, Bezzina, Connie R, Vandenberg, Jamie I, Verkerk, Arie O, Barge-Schaapveld, Daniela Q C M, Lodder, Elisabeth M

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The genetic basis of apparently idiopathic ventricular fibrillation: a retrospective overview von Verheul, Lisa M, van der Ree, Martijn H, Groeneveld, Sanne A, Mulder, Bart A, Christiaans, Imke, Kapel, Gijs F L, Alings, Marco, Bootsma, Marianne, Barge-Schaapveld, Daniela Q C M, Balt, Jippe C, Yap, Sing-Chien, Krapels, Ingrid P C, Ter Bekke, Rachel M A, Volders, Paul G A, van der Crabben, Saskia N, Postema, Pieter G, Wilde, Arthur A M, Dooijes, Dennis, Baas, Annette F, Hassink, Rutger J

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Testing an mHealth momentary assessment Routine Outcome Monitoring application: a focus on restoration of daily life positive mood states von van Os, Jim, Delespaul, Philippe, Barge, Daniela, Bakker, Roberto P

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Lessons from a lethal prolongation von Buiten, Maurits S, Egorova, Anastasia D, Barge-Schaapveld, Daniela Q C M, Piers, Sebastiaan R D

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What Is New in Dilatation of the Ascending Aorta? Review of Current Literature and Practical Advice for the Cardiologist von COZIJNSEN, Luc, BRAAM, Richard L, WAALEWIJN, Reinier A, SCHEPENS, Marc A. A. M, LOEYS, Bart L, VAN OOSTERHOUT, Matthijs F. M, BARGE-SCHAAPVELD, Daniela Q. C. M, MULDER, Barbara J. M

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Expanding the genetic and phenotypic spectrum of ACTA2-related vasculopathies in a Dutch cohort von van den Bersselaar, Lisa M., Verhagen, Judith M.A., Bekkers, Jos A., Kempers, Marlies, Houweling, Arjan C., Baars, Marieke, Overwater, Eline, Hilhorst-Hofstee, Yvonne, Barge-Schaapveld, Daniela Q.C.M., Rompen, Eline, Krapels, Ingrid P.C., Dulfer, Eelco, Wessels, Marja W., Loeys, Bart L., Verhagen, Hence J.M., Maugeri, Alessandra, Roos-Hesselink, Jolien W., Brüggenwirth, Hennie T., van de Laar, Ingrid M.B.H.

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Atypical Progeria Primarily Manifesting as Premature Cardiac Valvular Disease Segregates with LMNA -Gene Variants von Wu, Hoi W, Van de Peppel, Ivo P, Rutten, Julie W, Jukema, J Wouter, Aten, Emmelien, Jazet, Ingrid M, Koopmann, Tamara T, Barge-Schaapveld, Daniela Q C M, Ajmone Marsan, Nina

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The first titin (c.59926 + 1G > A) founder mutation associated with dilated cardiomyopathy von Hoorntje, Edgar T., van Spaendonck‐Zwarts, Karin Y., te Rijdt, Wouter P., Boven, Ludolf, Vink, Aryan, van der Smagt, Jasper J., Asselbergs, Folkert W., van Wijngaarden, Jan, Hennekam, Eric A., Pinto, Yigal M., Lekanne Deprez, Ronald H., Barge‐Schaapveld, Daniela Q.C.M., Bootsma, Marianne, Regieli, Jakub, Hoedemaekers, Yvonne M., Jongbloed, Jan D.H., van den Berg, Maarten P., van Tintelen, J. Peter

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Familial occurrence of mitral regurgitation in patients with mitral valve prolapse undergoing mitral valve surgery von Hiemstra, Yasmine L, Wijngaarden, Aniek L van, Bos, Mathilde W, Schalij, Martin J, Klautz, Robert JM, Bax, Jeroen J, Delgado, Victoria, Barge-Schaapveld, Daniela QCM, Marsan, Nina Ajmone

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