Suchergebnisse - Probst, Vincent

Adult-onset Still’s disease revealed by a complete atrioventricular block, totally regressive under corticosteroid therapy von Piriou, Pierre-Guillaume, Plessis, Julien, Letocart, Vincent, Piriou, Nicolas, Probst, Vincent, Néel, Antoine

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Inappropriate therapy after catheter ablation and subcutaneous implantable cardioverter-defibrillator von Minois, Damien, Malliet, Nicolas, Solnon, Aude, Lande, Gilles, Probst, Vincent, Gourraud, Jean-Baptiste

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Risk of ventricular arrhythmia in patients with myocardial infarction and non-obstructive coronary arteries and normal ejection fraction von Bière, Loïc, Niro, Marjorie, Pouliquen, Hervé, Gourraud, Jean-Baptiste, Prunier, Fabrice, Furber, Alain, Probst, Vincent

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Dynamic changes in ventricular depolarization during exercise in patients with Brugada syndrome von Romero, Daniel, Behar, Nathalie, Petit, Bertrand, Probst, Vincent, Sacher, Frederic, Mabo, Philippe, Hernández, Alfredo I.

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Differential calcium sensitivity in Na(V)1.5 mixed syndrome mutants von Abdelsayed, Mena, Baruteau, Alban‐Elouen, Gibbs, Karen, Sanatani, Shubhayan, Krahn, Andrew D., Probst, Vincent, Ruben, Peter C.

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The Brugada Syndrome: A Rare Arrhythmia Disorder with Complex Inheritance von Gourraud, Jean-Baptiste, Barc, Julien, Thollet, Aurélie, Le Scouarnec, Solena, Le Marec, Hervé, Schott, Jean-Jacques, Redon, Richard, Probst, Vincent

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Clinical outcome of patients with the Brugada type 1 electrocardiogram without prophylactic implantable cardioverter defibrillator in primary prevention: a cumulative analysis of s... von Delise, Pietro, Probst, Vincent, Allocca, Giuseppe, Sitta, Nadir, Sciarra, Luigi, Brugada, Josep, Kamakura, Shiro, Takagi, Masahiko, Giustetto, Carla, Calo, Leonardo

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TRPM4 non-selective cation channel variants in long QT syndrome von Hof, Thomas, Liu, Hui, Sallé, Laurent, Schott, Jean-Jacques, Ducreux, Corinne, Millat, Gilles, Chevalier, Philippe, Probst, Vincent, Guinamard, Romain, Bouvagnet, Patrice

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Genetics of syndromic and non-syndromic mitral valve prolapse von Le Tourneau, Thierry, Mérot, Jean, Rimbert, Antoine, Le Scouarnec, Solena, Probst, Vincent, Le Marec, Hervé, Levine, Robert A, Schott, Jean-Jacques

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Use of drugs with potential cardiac effect in the setting of SARS-CoV-2 infection von Sacher, Frederic, Fauchier, Laurent, Boveda, Serge, de Chillou, Christian, Defaye, Pascal, Deharo, Jean Claude, Gandjbakhch, Estelle, Probst, Vincent, Cohen, Ariel, Leclercq, Christophe

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

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Drugs and Brugada syndrome patients: review of the literature, recommendations and an up-to-date website (www.brugadadrugs.org) von Postema, Pieter G., Wolpert, Christian, Amin, Ahmad S., Probst, Vincent, Borggrefe, Martin, Roden, Dan M., Priori, Silvia G., Tan, Hanno L., Hiraoka, Masayasu, Brugada, Josep, Wilde, Arthur A.M.

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

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

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

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

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

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PQ Segment Depression in Short QT Syndrome Patients: A Novel Marker for Diagnosing Short QT Syndrome? von Tülümen, Erol, Giustetto, Carla, Wolpert C, Christian, Maury, Philippe, Anttonen, Olli, Probst, Vincent, Blanc, Jean-Jacques, Sbragia, Pascal, Scrocco, Chiara, Rudic, Boris, Veltmann, Christian, Sun, Yaxun, Gaita, Fiorenzo, Antzelevitch, Charles, Borggrefe, Martin, Schimpf, Rainer

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

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A standardised hERG phenotyping pipeline to evaluate KCNH2 genetic variant pathogenicity von 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

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