Single nucleotide polymorphisms and their association with QTc and left ventricular function in peripartum cardiomyopathy von Shaboodien, G, Viljoen, C, Ndibangwi, P, Hovelmann, J, Pearce, L, Haidari, S, Kotta, M C, Dagradi, F, Spazzolini, C, Kraus, S, Ntusi, N, Schwartz, P, Sliwa, K

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Novel human pathological mutations. Gene symbol: SCN5A. Disease: Brugada Syndrome von Crotti, Lia, Pedrazzini, M, Insolia, R, Cuoretti, A, Ghidoni, A, Dagradi, F, Taravelli, E, Chieffo, E, Vicentini, A, Schwartz, P J

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Gene symbol: KCNQ1. Disease: Long QT syndrome von Crotti, Lia, Ferrandi, C, Pedrazzini, M, Insolia, R, Cuoretti, A, Celano, G, Dagradi, F, Stramba-Badiale, M, Schwartz, P J

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Gene symbol: KCNH2. Disease: Long QT syndrome von Crotti, Lia, Crotti, L, Pedrazzini, M, Insolia, R, Ferrandi, C, Cuoretti, A, Gandolfi, E, Celano, G, Dagradi, F, Schwartz, P J

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Gene symbol: KCNQ1. Disease: Long QT syndrome von Crotti, Lia, Insolia, R, Ferrandi, C, Pedrazzini, M, Cuoretti, A, Gandolfi, E, Sanzo, A, Dagradi, F, Schwartz, P J

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Gene symbol: SCN5A. Disease: Brugada syndrome von Crotti, Lia, Ferrandi, C, Pedrazzini, M, Insolia, R, Cuoretti, A, Sanzo, A, Dagradi, F, De Ferrari, G M, Schwartz, P J

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P297Cardiac sympathetic denervation: evolving technique, expanding indications von Dusi, V, Pugliese, L, Castelletti, S, Dagradi, F, Crotti, L, Mori, A, Camporotondo, R, Raineri, C, Scelsi, L, Ghio, S, Savastano, S, Vicentini, A, Rordorf, R, Schwartz, P J, De Ferrari, G M

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Biventricular arrhythmogenic cardiomyopathy: a paradigmatic case von Calcagnino, M., Girardengo, G., Ghidoni, A., Kotta, M. C., Di Blasio, A., Revera, M., Torlasco, C., Perego, G., Bilo, B., Dagradi, F., Crotti, L., Parati, G., Schwartz, P. J., Cecchi, F.

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Gene symbol: KCNH2. Disease: Long QT syndrome von Crotti, Lia, Pedrazzini, M, Insolia, R, Ferrandi, C, Cuoretti, A, Celano, G, Gandolfi, E, Dagradi, F, Schwartz, P J

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Gene symbol: KCNH2. Disease: Long QT syndrome von Crotti, Lia, Pedrazzini, M, Ferrandi, C, Insolia, R, Cuoretti, A, Dagradi, F, Crimi, G, Coto, E, Reguero, J R, Schwartz, P J

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Gene symbol: SCN5A. Disease: Brugada syndrome von Crotti, Lia, Pedrazzini, M, Insolia, R, Ferrandi, C, Ghidoni, A, Sanzo, A, Dagradi, F, De Ferrari, G M, Swartz, P J

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Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls von Walsh, Roddy, Lahrouchi, Najim, Tadros, Rafik, Kyndt, Florence, Glinge, C, Postema, P.G, Amin, Ahmad S, Nannenberg, E.A, Ware, J.S, Whiffin, N, Mazzarotto, F, Korić-Milosavljević, D, Krijger, C, Arbelo, Elena, Babuty, D, Barajas-Martinez, H, Beckmann, B.M, Bézieau, S, Bos, J.M, Breckpot, J, Campuzano Larrea, Oscar, Castelletti, S, Celen, C, Clauss, S, Corveleyn, A, Crotti, Lia, Dagradi, F, de Asmundis, C, Denjoy, Isabelle, Dittmann, S, Ellinor, P.T, Ortuño, C.G, Giustetto, Carla, Gourraud, Jean Baptiste, Hazeki, D, Horie, M, Ishikawa, T, Itoh, H

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Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome von Lahrouchi, Najim, Tadros, Rafik, Crotti, Lia, Mizusawa, Yuka, Postema, Pieter G, Beekman, Leander, Walsh, Roddy, Hasegawa, Kanae, Barc, Julien, Ernsting, Marko, Turkowski, Kari L, Mazzanti, Andrea, Beckmann, Britt M, Shimamoto, Keiko, Diamant, U.B, Wijeyeratne, Yanushi D, Kucho, Y, Robyns, T, Ishikawa, T, Arbelo, Elena, Christiansen, M, Winbo, A, Jabbari, R, Lubitz, S.A, Steinfurt, J, Rudic, B, Loeys, B, Shoemaker, M.B, Weeke, P.E, Pfeiffer, R, Davies, B, Andorin, Antoine, Hofman, N, Dagradi, F, Pedrazzini, M, Tester, D.J, Bos, J.M, Sarquella Brugada, Geòrgia, Campuzano Larrea, Oscar, Platonov, P.G

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Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry von Crotti, L, Spazzolini, C, Tester, DJ, Ghidoni, A, Baruteau, A-E, Beckmann, B-M, Behr, ER, Bennett, JS, Bezzina, CR, Bhuiyan, ZA, Celiker, A, Cerrone, M, Dagradi, F, De Ferrari, GM, Etheridge, SP, Fatah, M, Garcia-Pavia, P, Al-Ghamdi, S, Hamilton, RM, Al-Hassnan, ZN, Horie, M, Jimenez-Jaimez, J, Kanter, RJ, Kaski, JP, Kotta, M-C, Lahrouchi, N, Makita, N, Norrish, G, Odland, HH, Ohno, S, Papagiannis, J, Parati, G, Sekarski, N, Tveten, K, Vatta, M, Webster, G, Wilde, AAM, Wojciak, J, George, AL, Ackerman, MJ, Schwartz, PJ

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SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroups von Baruteau, A-E, Kyndt, F, Behr, ER, Vink, AS, Lachaud, M, Joong, A, Schott, J-J, Horie, M, Denjoy, I, Crotti, L, Shimizu, W, Bos, JM, Stephenson, EA, Wong, L, Abrams, DJ, Davis, AM, Winbo, A, Dubin, AM, Sanatani, S, Liberman, L, Kaski, JP, Rudic, B, Kwok, SY, Rieubland, C, Tfelt-Hansen, J, Van Hare, GF, Guyomarc'h-Delasalle, B, Blom, NA, Wijeyeratne, YD, Gourraud, J-B, Le Marec, H, Ozawa, J, Fressart, V, Lupoglazoff, J-M, Dagradi, F, Spazzolini, C, Aiba, T, Tester, DJ, Zahavich, LA, Beauséjour-Ladouceur, V, Jadhav, M, Skinner, JR, Franciosi, S, Krahn, AD, Abdelsayed, M, Ruben, PC, Yung, T-C, Ackerman, MJ, Wilde, AA, Schwartz, PJ, Probst, V

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Energy drinks and sudden death: If it swims like a duck von Schwartz, Peter J., Giovenzana, Fulvio L.F., Dagradi, Federica

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Top stories on congenital long QT syndrome von Schwartz, Peter J., Dagradi, Federica, Giovenzana, Fulvio L.F.

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Long QT syndrome: importance of reassessing arrhythmic risk after treatment initiation von Dusi, Veronica, Dagradi, Federica, Spazzolini, Carla, Crotti, Lia, Cerea, Paolo, Giovenzana, Fulvio L F, Musu, Giulia, Pedrazzini, Matteo, Torchio, Margherita, Schwartz, Peter J

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Therapeutic Efficacy of Mexiletine for Long QT Syndrome Type 2: Evidence From Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes, Transgenic Rabbits, and Patients von Crotti, Lia, Neves, Raquel, Dagradi, Federica, Musu, Giulia, Giannetti, Federica, Bos, J Martijn, Barbieri, Miriam, Cerea, Paolo, Giovenzana, Fulvio L F, Torchio, Margherita, Mura, Manuela, Gnecchi, Massimiliano, Conte, Giulio, Auricchio, Angelo, Sala, Luca, Odening, Katja E, Ackerman, Michael J, Schwartz, Peter J

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Mothers with long QT syndrome are at increased risk for fetal death: findings from a multicenter international study von Cuneo, Bettina F., Kaizer, Alexander M., Clur, Sally Ann, Swan, Heikki, Herberg, Ulrike, Winbo, Annika, Rydberg, Annika, Haugaa, Kristina, Etheridge, Susan, Ackerman, Michael J., Dagradi, Federica, Killen, Stacy A.S., Wacker-Gussmann, Annette, Benson, D. Woodrow, Wilde, A.A.M., Pan, Zhaoxing, Lam, Aimee, Spazzolini, Carla, Horigome, Hitoshi, Schwartz, Peter J.

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