Inappropriate therapy after catheter ablation and subcutaneous implantable cardioverter-defibrillator

por Minois, Damien, Malliet, Nicolas, Solnon, Aude, Lande, Gilles, Probst, Vincent, Gourraud, Jean-Baptiste
Publicado 2020

Atrial flutter radiofrequency ablation in the setting of left isomerism and repaired single atrium: First case

por Arnaud, Marine, Le Gloan, Laurianne, Andorin, Antoine, Solnon, Aude, Gourraud, Jean-Baptiste, Lande, Gilles
Publicado 2021

Risk of ventricular arrhythmia in patients with myocardial infarction and non-obstructive coronary arteries and normal ejection fraction

por Bière, Loïc, Niro, Marjorie, Pouliquen, Hervé, Gourraud, Jean-Baptiste, Prunier, Fabrice, Furber, Alain, Probst, Vincent
Publicado 2017

Electrical Storm Ablation in a Patient in Cardiogenic Shock Supported by Impella 5.0

por Le Ruz, Robin, Lande, Gilles, Lepoivre, Thierry, David, Charles-Henri, Michel, Magali, Gourraud, Jean-Baptiste
Publicado 2021

The Brugada Syndrome: A Rare Arrhythmia Disorder with Complex Inheritance

por Gourraud, Jean-Baptiste, Barc, Julien, Thollet, Aurélie, Le Scouarnec, Solena, Le Marec, Hervé, Schott, Jean-Jacques, Redon, Richard, Probst, Vincent
Publicado 2016

Assessment of cardiac resynchronisation therapy in patients with wide QRS and non-specific intraventricular conduction delay: rationale and design of the multicentre randomised NIC...

por Eschalier, Romain, Ploux, Sylvain, Pereira, Bruno, Clémenty, Nicolas, Da Costa, Antoine, Defaye, Pascal, Garrigue, Stéphane, Gourraud, Jean-Baptiste, Gras, Daniel, Guy-Moyat, Benoît, Leclercq, Christophe, Mondoly, Pierre, Bordachar, Pierre
Publicado 2016

A consistent arrhythmogenic trait in Brugada syndrome cellular phenotype

por Al Sayed, Zeina R., Jouni, Mariam, Gourraud, Jean‐Baptiste, Belbachir, Nadjet, Barc, Julien, Girardeau, Aurore, Forest, Virginie, Derevier, Aude, Gaignerie, Anne, Chariau, Caroline, Cimarosti, Bastien, Canac, Robin, Olchesqui, Pierre, Charpentier, Eric, Schott, Jean‐Jacques, Redon, Richard, Baró, Isabelle, Probst, Vincent, Charpentier, Flavien, Loussouarn, Gildas, Zibara, Kazem, Lamirault, Guillaume, Lemarchand, Patricia, Gaborit, Nathalie
Publicado 2021

Dysfunction of the Voltage‐Gated K(+) Channel β2 Subunit in a Familial Case of Brugada Syndrome

por Portero, Vincent, Le Scouarnec, Solena, Es‐Salah‐Lamoureux, Zeineb, Burel, Sophie, Gourraud, Jean‐Baptiste, Bonnaud, Stéphanie, Lindenbaum, Pierre, Simonet, Floriane, Violleau, Jade, Baron, Estelle, Moreau, Eléonore, Scott, Carol, Chatel, Stéphanie, Loussouarn, Gildas, O'Hara, Thomas, Mabo, Philippe, Dina, Christian, Le Marec, Hervé, Schott, Jean‐Jacques, Probst, Vincent, Baró, Isabelle, Marionneau, Céline, Charpentier, Flavien, Redon, Richard
Publicado 2016

Rationale and Design of the Randomized Bayesian Multicenter COME-TAVI Trial in Patients With a New Onset Left Bundle Branch Block

por Rivard, Lena, Nault, Isabelle, Krahn, Andrew D., Daneault, Benoit, Roux, Jean-Francois, Natarajan, Madhu, Healey, Jeffrey S., Quadros, Kenneth, Sandhu, Roopinder K., Kouz, Remi, Greiss, Isabelle, Leong-Sit, Peter, Gourraud, Jean Baptiste, Ben Ali, Walid, Asgar, Anita, Aguilar, Martin, Bonan, Raoul, Cadrin-Tourigny, Julia, Cartier, Raymond, Dorval, Jean-Francois, Dubuc, Marc, Dürrleman, Nicolas, Dyrda, Katia, Guerra, Peter, Ibrahim, Marina, Ibrahim, Reda, Macle, Laurent, Mondesert, Blandine, Moss, Emmanuel, Raymond-Paquin, Alexandre, Roy, Denis, Tadros, Rafik, Thibault, Bernard, Talajic, Mario, Nozza, Anna, Guertin, Marie-Claude, Khairy, Paul
Publicado 2023

Arrhythmic risk prediction in arrhythmogenic right ventricular cardiomyopathy: external validation of the arrhythmogenic right ventricular cardiomyopathy risk calculator( )

por Jordà, Paloma, Bosman, Laurens P, Gasperetti, Alessio, Mazzanti, Andrea, Gourraud, Jean Baptiste, Davies, Brianna, Frederiksen, Tanja Charlotte, Weidmann, Zoraida Moreno, Di Marco, Andrea, Roberts, Jason D, MacIntyre, Ciorsti, Seifer, Colette, Delinière, Antoine, Alqarawi, Wael, Kukavica, Deni, Minois, Damien, Trancuccio, Alessandro, Arnaud, Marine, Targetti, Mattia, Martino, Annamaria, Oliviero, Giada, Pipilas, Daniel C, Carbucicchio, Corrado, Compagnucci, Paolo, Dello Russo, Antonio, Olivotto, Iacopo, Calò, Leonardo, Lubitz, Steven A, Cutler, Michael J, Chevalier, Philippe, Arbelo, Elena, Priori, Silvia Giuliana, Healey, Jeffrey S, Calkins, Hugh, Casella, Michela, Jensen, Henrik Kjærulf, Tondo, Claudio, Tadros, Rafik, James, Cynthia A, Krahn, Andrew D, Cadrin-Tourigny, Julia
Publicado 2022

SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A Families

por Wijeyeratne, Yanushi D., Tanck, Michael W., Mizusawa, Yuka, Batchvarov, Velislav, Barc, Julien, Crotti, Lia, Bos, J. Martijn, Tester, David J., Muir, Alison, Veltmann, Christian, Ohno, Seiko, Page, Stephen P., Galvin, Joseph, Tadros, Rafik, Muggenthaler, Martina, Raju, Hariharan, Denjoy, Isabelle, Schott, Jean-Jacques, Gourraud, Jean-Baptiste, Skoric-Milosavljevic, Doris, Nannenberg, Eline A., Redon, Richard, Papadakis, Michael, Kyndt, Florence, Dagradi, Federica, Castelletti, Silvia, Torchio, Margherita, Meitinger, Thomas, Lichtner, Peter, Ishikawa, Taisuke, Wilde, Arthur A.M., Takahashi, Kazuhiro, Sharma, Sanjay, Roden, Dan M., Borggrefe, Martin M., McKeown, Pascal P., Shimizu, Wataru, Horie, Minoru, Makita, Naomasa, Aiba, Takeshi, Ackerman, Michael J., Schwartz, Peter J., Probst, Vincent, Bezzina, Connie R., Behr, Elijah R.
Publicado 2020

Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

por 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, Ulla-Britt, Wijeyeratne, Yanushi D., Kucho, Yu, Robyns, Tomas, Ishikawa, Taisuke, Arbelo, Elena, Christiansen, Michael, Winbo, Annika, Jabbari, Reza, Lubitz, Steven A., Steinfurt, Johannes, Rudic, Boris, Loeys, Bart, Shoemaker, M. Ben, Weeke, Peter E., Pfeiffer, Ryan, Davies, Brianna, Andorin, Antoine, Hofman, Nynke, Dagradi, Federica, Pedrazzini, Matteo, Tester, David J., Bos, J. Martijn, Sarquella-Brugada, Georgia, Campuzano, Óscar, Platonov, Pyotr G., Stallmeyer, Birgit, Zumhagen, Sven, Nannenberg, Eline A., Veldink, Jan H., van den Berg, Leonard H., Al-Chalabi, Ammar, Shaw, Christopher E., Shaw, Pamela J., Morrison, Karen E., Andersen, Peter M., Müller-Nurasyid, Martina, Cusi, Daniele, Barlassina, Cristina, Galan, Pilar, Lathrop, Mark, Munter, Markus, Werge, Thomas, Ribasés, Marta, Aung, Tin, Khor, Chiea C., Ozaki, Mineo, Lichtner, Peter, Meitinger, Thomas, van Tintelen, J. Peter, Hoedemaekers, Yvonne, Denjoy, Isabelle, Leenhardt, Antoine, Napolitano, Carlo, Shimizu, Wataru, Schott, Jean-Jacques, Gourraud, Jean-Baptiste, Makiyama, Takeru, Ohno, Seiko, Itoh, Hideki, Krahn, Andrew D., Antzelevitch, Charles, Roden, Dan M., Saenen, Johan, Borggrefe, Martin, Odening, Katja E., Ellinor, Patrick T., Tfelt-Hansen, Jacob, Skinner, Jonathan R., van den Berg, Maarten P., Olesen, Morten Salling, Brugada, Josep, Brugada, Ramón, Makita, Naomasa, Breckpot, Jeroen, Yoshinaga, Masao, Behr, Elijah R., Rydberg, Annika, Aiba, Takeshi, Kääb, Stefan, Priori, Silvia G., Guicheney, Pascale, Tan, Hanno L., Newton-Cheh, Christopher, Ackerman, Michael J., Schwartz, Peter J., Schulze-Bahr, Eric, Probst, Vincent, Horie, Minoru, Wilde, Arthur A., Tanck, Michael W.T., Bezzina, Connie R.
Publicado 2020

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

por Walsh, Roddy, Lahrouchi, Najim, Tadros, Rafik, Kyndt, Florence, Glinge, Charlotte, Postema, Pieter G., Amin, Ahmad S., Nannenberg, Eline A., Ware, James S., Whiffin, Nicola, Mazzarotto, Francesco, Škorić-Milosavljević, Doris, Krijger, Christian, Arbelo, Elena, Babuty, Dominique, Barajas-Martinez, Hector, Beckmann, Britt M., Bézieau, Stéphane, Bos, J. Martijn, Breckpot, Jeroen, Campuzano, Oscar, Castelletti, Silvia, Celen, Candan, Clauss, Sebastian, Corveleyn, Anniek, Crotti, Lia, Dagradi, Federica, de Asmundis, Carlo, Denjoy, Isabelle, Dittmann, Sven, Ellinor, Patrick T., Ortuño, Cristina Gil, Giustetto, Carla, Gourraud, Jean-Baptiste, Hazeki, Daisuke, Horie, Minoru, Ishikawa, Taisuke, Itoh, Hideki, Kaneko, Yoshiaki, Kanters, Jørgen K., Kimoto, Hiroki, Kotta, Maria-Christina, Krapels, Ingrid P. C., Kurabayashi, Masahiko, Lazarte, Julieta, Leenhardt, Antoine, Loeys, Bart L., Lundin, Catarina, Makiyama, Takeru, Mansourati, Jacques, Martins, Raphaël P., Mazzanti, Andrea, Mörner, Stellan, Napolitano, Carlo, Ohkubo, Kimie, Papadakis, Michael, Rudic, Boris, Molina, Maria Sabater, Sacher, Frédéric, Sahin, Hatice, Sarquella-Brugada, Georgia, Sebastiano, Regina, Sharma, Sanjay, Sheppard, Mary N., Shimamoto, Keiko, Shoemaker, M. Benjamin, Stallmeyer, Birgit, Steinfurt, Johannes, Tanaka, Yuji, Tester, David J., Usuda, Keisuke, van der Zwaag, Paul A., Van Dooren, Sonia, Van Laer, Lut, Winbo, Annika, Winkel, Bo G., Yamagata, Kenichiro, Zumhagen, Sven, Volders, Paul G. A., Lubitz, Steven A., Antzelevitch, Charles, Platonov, Pyotr G., Odening, Katja E., Roden, Dan M., Roberts, Jason D., Skinner, Jonathan R., Tfelt-Hansen, Jacob, van den Berg, Maarten P., Olesen, Morten S., Lambiase, Pier D., Borggrefe, Martin, Hayashi, Kenshi, Rydberg, Annika, Nakajima, Tadashi, Yoshinaga, Masao, Saenen, Johan B., Kääb, Stefan, Brugada, Pedro, Robyns, Tomas, Giachino, Daniela F., Ackerman, Michael J., Brugada, Ramon, Brugada, Josep, Gimeno, Juan R., Hasdemir, Can, Guicheney, Pascale, Priori, Silvia G., Schulze-Bahr, Eric, Makita, Naomasa, Schwartz, Peter J., Shimizu, Wataru, Aiba, Takeshi, Schott, Jean-Jacques, Redon, Richard, Ohno, Seiko, Probst, Vincent, Behr, Elijah R., Barc, Julien, Bezzina, Connie R.
Publicado 2020