Mutations in DCHS1 cause mitral valve prolapse von Durst, Ronen, Sauls, Kimberly, Peal, David S., deVlaming, Annemarieke, Toomer, Katelynn, Leyne, Maire, Salani, Monica, Talkowski, Michael E., Brand, Harrison, Perrocheau, Maëlle, Simpson, Charles, Jett, Christopher, Stone, Matthew R., Charles, Florie, Chiang, Colby, Lynch, Stacey N., Bouatia-Naji, Nabila, Delling, Francesca N., Freed, Lisa A., Tribouilloy, Christophe, Le Tourneau, Thierry, LeMarec, Hervé, Fernandez-Friera, Leticia, Solis, Jorge, Trujillano, Daniel, Ossowski, Stephan, Estivill, Xavier, Dina, Christian, Bruneval, Patrick, Chester, Adrian, Schott, Jean-Jacques, Irvine, Kenneth D., Mao, Yaopan, Wessels, Andy, Motiwala, Tahirali, Puceat, Michel, Tsukasaki, Yoshikazu, Menick, Donald R., Kasiganesan, Harinath, Nie, Xingju, Broome, Ann-Marie, Williams, Katherine, Johnson, Amanda, Markwald, Roger R., Jeunemaitre, Xavier, Hagege, Albert, Levine, Robert A., Milan, David J., Norris, Russell A., Slaugenhaupt, Susan A.

Volltext

Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non–SCN5A-related patients von Smits, Jeroen P.P, Eckardt, Lars, Probst, Vincent, Bezzina, Connie R, Schott, Jean Jacques, Remme, Carol Ann, Haverkamp, Wilhelm, Breithardt, Günter, Escande, Denis, Schulze-Bahr, Eric, LeMarec, Hervé, Wilde, Arthur A.M

Volltext

Torsades de pointes complicating atrioventricular block: Evidence for a genetic predisposition von Chevalier, Philippe, MD, PhD, Bellocq, Chloé, PhD, Millat, Gilles, PhD, Piqueras, Eric, MD, Potet, Franck, PhD, Schott, Jean-Jacques, PhD, Baró, Isabelle, PhD, Lemarec, Hervé, MD, PhD, Barhanin, Jacques, PhD, Rousson, Robert, MD, PhD, Rodriguez-Lafrasse, Claire, PhD

Volltext

Are Women with Severely Symptomatic Brugada Syndrome Different from Men? von SACHER, FRÉDÉRIC, MEREGALLI, PAOLA, VELTMANN, CHRISTIAN, FIELD, MICHAEL E, SOLNON, AUDE, BRU, PAUL, ABBEY, SÉLIM, JAÏS, PIERRE, TAN, HANNO L, WOLPERT, CHRISTIAN, LANDE, GILLES, BERTAULT, VALÉRIE, DERVAL, NICOLAS, BABUTY, DOMINIQUE, LACROIX, DOMINIQUE, BOVEDA, SERGE, MAURY, PHILIPPE, HOCINI, MÉLÈZE, CLÉMENTY, JACQUES, MABO, PHILIPPE, LEMAREC, HERVÉ, MANSOURATI, JACQUES, BORGGREFE, MARTIN, WILDE, ARTHUR, HAÏSSAGUERRE, MICHEL, PROBST, VINCENT

Volltext

The ajmaline challenge and a strange ECG: reply von Veltmann, Christian, Wolpert, Christian, Schimpf, Rainer, Mabo, Philippe, LeMarec, Herve, Borggrefe, Martin, Probst, Vincent

Volltext

Genetic association analyses highlight biological pathways underlying mitral valve prolapse von Dina, Christian, Bouatia-Naji, Nabila, Tucker, Nathan, Delling, Francesca N, Toomer, Katelynn, Durst, Ronen, Perrocheau, Maelle, Fernandez-Friera, Leticia, Solis, Jorge, Le Tourneau, Thierry, Chen, Ming-Huei, Probst, Vincent, Bosse, Yohan, Pibarot, Philippe, Zelenika, Diana, Lathrop, Mark, Hercberg, Serge, Roussel, Ronan, Benjamin, Emelia J, Bonnet, Fabrice, Lo, Su Hao, Dolmatova, Elena, Simonet, Floriane, Lecointe, Simon, Kyndt, Florence, Redon, Richard, Le Marec, Hervé, Froguel, Philippe, Ellinor, Patrick T, Vasan, Ramachandran S, Bruneval, Patrick, Markwald, Roger R, Norris, Russell A, Milan, David J, Slaugenhaupt, Susan A, Levine, Robert A, Schott, Jean-Jacques, Hagege, Albert A, Jeunemaitre, Xavier

Volltext

Brugada syndrome. Report of the second consensus conference. Endorsed by the Heart Rhythm Society and the European Heart Rhythm Association von ANTZELEVITCH, Charles, BRUGADA, Pedro, SHIMIZU, Wataru, SCHULZE-BAHR, Eric, TAN, Hanno, WILDE, Arthur, BORGGREFE, Martin, BRUGADA, Josep, BRUGADA, Ramon, CORRADO, Domenico, GUSSAK, Ihor, LEMAREC, Herve, NADEMANEE, Koonlawee, PEREZ RIERA, Andres Ricardo

Volltext

Mutations in DCHS1 Cause Mitral Valve Prolapse von Durst, Ronen, Sauls, Kimberly, Peal, David S, deVlaming, Annemarieke, Toomer, Katelynn, Leyne, Maire, Salani, Monica, Talkowski, Michael E, Brand, Harrison, Perrocheau, Maëlle, Simpson, Charles, Jett, Christopher, Stone, Matthew R, Charles, Florie, Chiang, Colby, Lynch, Stacey N, Bouatia-Naji, Nabila, Delling, Francesca N, Freed, Lisa A, Tribouilloy, Christophe, Le Tourneau, Thierry, LeMarec, Hervé, Fernandez-Friera, Leticia, Solis, Jorge, Trujillano, Daniel, Ossowski, Stephan, Estivill, Xavier, Dina, Christian, Bruneval, Patrick, Chester, Adrian, Schott, Jean-Jacques, Irvine, Kenneth D, Mao, Yaopan, Wessels, Andy, Motiwala, Tahirali, Puceat, Michel, Tsukasaki, Yoshikazu, Menick, Donald R, Kasiganesan, Harinath, Nie, Xingju, Broome, Ann-Marie, Williams, Katherine, Johnson, Amanda, Markwald, Roger R, Jeunemaitre, Xavier, Hagege, Albert, Levine, Robert A, Milan, David J, Norris, Russell A, Slaugenhaupt, Susan A

Volltext

Brugada syndrome: report of the second consensus conference von Antzelevitch, Charles, Brugada, Pedro, Borggrefe, Martin, Brugada, Josep, Brugada, Ramon, Corrado, Domenico, Gussak, Ihor, LeMarec, Herve, Nademanee, Koonlawee, Perez Riera, Andres Ricardo, Shimizu, Wataru, Schulze-Bahr, Eric, Tan, Hanno, Wilde, Arthur

Volltext

Long-term prognosis of individuals with right precordial ST-segment-elevation Brugada syndrome von ECKARDT, Lars, PROBST, Vincent, BORGGREFE, Martin, LEMAREC, Herve, BÖCKER, Dirk, WILDE, Arthur A. M, SMITS, Jeroen P. P, BAHR, Eric Schulze, WOLPERT, Christian, SCHIMPF, Rainer, WICHTER, Thomas, BOISSEAU, Pierre, HEINECKE, Achim, BREITHARDT, Günter

Volltext

287 Early repolarization syndrome: Valsalva maneuver in familial screening von Gourraud, Jean-Baptiste, Sacher, Frédéric, Redon, Richard, Schott, Jean-Jacques, Chavernac, Pascal, Lemarec, Hervé, Mabo, Philippe, Haïssaguerre, Michel, Probst, Vincent

Volltext

Abstract 8808: Early Repolarization Syndrome: Valsalva Maneuver in Familial Screening von Gourraud, Jean Baptiste, Le Scouarnec, Solena, Sacher, Frederic, Chatel, Stephanie, Chavernac, Pascal, Mabo, Philippe, Redon, Richard, Schott, Jean Jacques, Lemarec, Herve, Haissaguerre, Michel, Probst, Vincent

Volltext

Abstract 18977: Non-Syndromic Mitral Valve Prolapse From Gene Mutations to Modifiable Mechanisms von Norris, Russell, Sauls, Kimberly, Durst, Ronen, Peal, David, Toomer, Katelynn, Leyne, Maire, Talkowski, Michael E, Brand, Harrison, Perrocheau, Maelle, Lynch, Stacey N, Bouaia-Naji, Nabila, Delling, Francesca N, Freed, Lisa A, Le Tourneau, Thierry, LeMarec, Herve, Estivill, Xavier, Fernandez-Friera, Leticia, Dina, Christian, Solis, Jorge, Trujillano, Daniel, Irvine, Kenneth D, Mao, Yaopan, Ossowski, Stephan, Wessels, Any, Menick, Donald, Kasiganesan, Harinath, Bromme, Ann-Marie, Williams, Katherine, Schott, Jean-Jacques, Hagege, Albert A, Jeunemaitre, Xavier, Markwald, Roger R, Milan, David J, Levine, Robert A, Slaugenhaupt, Susan

Volltext

Long-term prognosis of individuals with right predordial ST-elevation - Brugada syndrome von Eckardt, Lars, Probst, Vincent, Smits, Jereon, Schulze-Bahr, Eric, Wichter, Thomas, Lemarec, Herve, Wolpert, Christian, Breithardt, Günter, Borggrefe, Martin, Boecker, Dirk, Wilde, Arthur

Volltext

Multicenter study of prophylactic ICD implantation in Brugada syndrome von Sacher, Frédéric, Probst, Vincent, Babuty, Dominique, Mizon-Gerard, Frederique, Maury, Philippe, Mansourati, Jacques, Mabo, Philippe, Pasquié, Jean-Luc, Laborderie, Julien, Chevallier, Jean-Michel, Vally, Nathalie, Salvador, Michèle, Sanders, Prashantan, Hocini, MélÈze, Garrigue, Stéphane, Jaïs, Pierre, Clémenty, Jacques, Haïssaguerre, Michel, Lemarec, Herve

Volltext

Predictive value of electrophysiologic studies during treatment of ventricular tachycardia with the beta-blocking agent nadolol von Leclercq, Jean-François, Leenhardt, Antoine, Lemarec, Hervé, Clémenty, Jacques, Hermida, Jean-Sylvain, Sebag, Claude, Aliot, Etienne

Volltext

Brugada Syndrome: Report of the Second Consensus Conference

Volltext

Mutations in the gene encoding filamin a as a cause for familial cardiac valvular dystrophy von KYNDT, Florence, GUEFFET, Jean-Pierre, NEWBURY-ECOB, Ruth, TRAN, Vinh, YOUNG, Ian, TROCHU, Jean-Noël, LE MAREC, Hervé, SCHOTT, Jean-Jacques, PROBST, Vincent, JAAFAR, Philippe, LEGENDRE, Antoine, LE BOUFFANT, Francoise, TOQUET, Claire, ROY, Estelle, MCGREGOR, Lesley, LYNCH, Sally Ann

Volltext

Mapping of a gene for long QT syndrome to chromosome 4q25-27 von SCHOTT, J.-J, CHARPENTIER, F, LE MAREC, H, PASCAL, O, PELTIER, S, FOLEY, P, DROUIN, E, BOUHOUR, J.-B, DONNELLY, P, VERGNAUD, G, BACHNER, L, MOISAN, J.-P

Volltext

Electrophysiologic characteristics of cells spanning the left ventricular wall of human heart: Evidence for presence of M cells von Drouin, Emmanuel, Charpentier, Flavien, Gauthier, Chantal, Laurent, Karine, Le Marec, Herve

Volltext