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

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

Dynamic changes in ventricular depolarization during exercise in patients with Brugada syndrome

por Romero, Daniel, Behar, Nathalie, Petit, Bertrand, Probst, Vincent, Sacher, Frederic, Mabo, Philippe, Hernández, Alfredo I.
Publicado 2020

Low rates of inappropriate shocks in contemporary real-world implantable cardioverter defibrillator patients: the CARAT observational study

por Dichtl, Wolfgang, De Sousa, João, Rubin Lopez, Jose Manuel, Campo, Enrique Garcia, Gutleben, Klaus-Jürgen, Poezevara, Yann, Probst, Vincent
Publicado 2023

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

Clinical outcome of patients with the Brugada type 1 electrocardiogram without prophylactic implantable cardioverter defibrillator in primary prevention: a cumulative analysis of s...

por Delise, Pietro, Probst, Vincent, Allocca, Giuseppe, Sitta, Nadir, Sciarra, Luigi, Brugada, Josep, Kamakura, Shiro, Takagi, Masahiko, Giustetto, Carla, Calo, Leonardo
Publicado 2018

TRPM4 non-selective cation channel variants in long QT syndrome

por Hof, Thomas, Liu, Hui, Sallé, Laurent, Schott, Jean-Jacques, Ducreux, Corinne, Millat, Gilles, Chevalier, Philippe, Probst, Vincent, Guinamard, Romain, Bouvagnet, Patrice
Publicado 2017

Use of drugs with potential cardiac effect in the setting of SARS-CoV-2 infection

por Sacher, Frederic, Fauchier, Laurent, Boveda, Serge, de Chillou, Christian, Defaye, Pascal, Deharo, Jean Claude, Gandjbakhch, Estelle, Probst, Vincent, Cohen, Ariel, Leclercq, Christophe
Publicado 2020

From gene-discovery to gene-tailored clinical management: 25 years of research in channelopathies and cardiomyopathies

por Crotti, Lia, Brugada, Pedro, Calkins, Hugh, Chevalier, Philippe, Conte, Giulio, Finocchiaro, Gherardo, Postema, Pieter G, Probst, Vincent, Schwartz, Peter J, Behr, Elijah R
Publicado 2023

Molecular Genetics and Functional Anomalies in a Series of 248 Brugada Cases with 11 Mutations in the TRPM4 Channel

por Liu, Hui, Chatel, Stéphanie, Simard, Christophe, Syam, Ninda, Salle, Laurent, Probst, Vincent, Morel, Julie, Millat, Gilles, Lopez, Michel, Abriel, Hugues, Schott, Jean-Jacques, Guinamard, Romain, Bouvagnet, Patrice
Publicado 2013

Variants of Transient Receptor Potential Melastatin Member 4 in Childhood Atrioventricular Block

por Syam, Ninda, Chatel, Stéphanie, Ozhathil, Lijo Cherian, Sottas, Valentin, Rougier, Jean‐Sébastien, Baruteau, Alban, Baron, Estelle, Amarouch, Mohamed‐Yassine, Daumy, Xavier, Probst, Vincent, Schott, Jean‐Jacques, Abriel, Hugues
Publicado 2016

An African loss-of-function CACNA1C variant p.T1787M associated with a risk of ventricular fibrillation

por Blancard, Malorie, Debbiche, Amal, Kato, Koichi, Cardin, Christelle, Sabrina, Guichard, Gandjbakhch, Estelle, Probst, Vincent, Haissaguerre, Michel, Extramiana, Fabrice, Hocini, Mélèze, Olivier, Geoffroy, Leenhardt, Antoine, Guicheney, Pascale, Rougier, Jean-Sébastien
Publicado 2018

SARS-CoV-2, COVID-19, and inherited arrhythmia syndromes

por Wu, Cheng-I, Postema, Pieter G., Arbelo, Elena, Behr, Elijah R., Bezzina, Connie R., Napolitano, Carlo, Robyns, Tomas, Probst, Vincent, Schulze-Bahr, Eric, Remme, Carol Ann, Wilde, Arthur A.M.
Publicado 2020

Abnormal Cellular Phenotypes Induced by Three TMPO/LAP2 Variants Identified in Men with Cardiomyopathies

por Vadrot, Nathalie, Ader, Flavie, Moulin, Maryline, Merlant, Marie, Chapon, Françoise, Gandjbakhch, Estelle, Labombarda, Fabien, Maragnes, Pascale, Réant, Patricia, Rooryck, Caroline, Probst, Vincent, Donal, Erwan, Richard, Pascale, Ferreiro, Ana, Buendia, Brigitte
Publicado 2023

Familial screening in case of acute myocarditis reveals inherited arrhythmogenic left ventricular cardiomyopathies

por Piriou, Nicolas, Marteau, Lara, Kyndt, Florence, Serfaty, Jean Michel, Toquet, Claire, Le Gloan, Laurianne, Warin‐Fresse, Karine, Guijarro, Damien, Le Tourneau, Thierry, Conan, Emilie, Thollet, Aurélie, Probst, Vincent, Trochu, Jean‐Noël
Publicado 2020

Diagnosis and management of subcutaneous implantable cardioverter‐defibrillator infections based on process mapping

por Baddour, Larry M., Weiss, Raul, Mark, George E., El‐Chami, Mikhael F., Biffi, Mauro, Probst, Vincent, Lambiase, Pier D., Miller, Marc A., McClernon, Timothy, Hansen, Linda K., Knight, Bradley P.
Publicado 2020

Process mapping strategies to prevent subcutaneous implantable cardioverter‐defibrillator infections

por Weiss, Raul, Mark, George E., El‐Chami, Mikhael F., Biffi, Mauro, Probst, Vincent, Lambiase, Pier D., Miller, Marc A., McClernon, Timothy, Hansen, Linda K., Knight, Bradley P., Baddour, Larry M.
Publicado 2022

Idiopathic Ventricular Fibrillation: Role of Purkinje System and Microstructural Myocardial Abnormalities

por Haïssaguerre, Michel, Duchateau, Josselin, Dubois, Remi, Hocini, Mélèze, Cheniti, Ghassen, Sacher, Frederic, Lavergne, Thomas, Probst, Vincent, Surget, Elodie, Vigmond, Ed, Welte, Nicolas, Chauvel, Remi, Derval, Nicolas, Pambrun, Thomas, Jais, Pierre, Nademanee, Wee, Bernus, Olivier
Publicado 2020

A standardised hERG phenotyping pipeline to evaluate KCNH2 genetic variant pathogenicity

por Oliveira‐Mendes, Barbara, Feliciangeli, Sylvain, Ménard, Mélissa, Chatelain, Frank, Alameh, Malak, Montnach, Jérôme, Nicolas, Sébastien, Ollivier, Béatrice, Barc, Julien, Baró, Isabelle, Schott, Jean‐Jacques, Probst, Vincent, Kyndt, Florence, Denjoy, Isabelle, Lesage, Florian, Loussouarn, Gildas, De Waard, Michel
Publicado 2021

Variable Na(v)1.5 Protein Expression from the Wild-Type Allele Correlates with the Penetrance of Cardiac Conduction Disease in the Scn5a (+/−) Mouse Model

por Leoni, Anne-Laure, Gavillet, Bruno, Rougier, Jean-Sébastien, Marionneau, Céline, Probst, Vincent, Le Scouarnec, Solena, Schott, Jean-Jacques, Demolombe, Sophie, Bruneval, Patrick, Huang, Christopher L. H., Colledge, William H., Grace, Andrew A., Le Marec, Hervé, Wilde, Arthur A., Mohler, Peter J., Escande, Denis, Abriel, Hugues, Charpentier, Flavien
Publicado 2010