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Outcome after implantation of a cardioverter-defibrillator in patients with Brugada syndrome: a multicenter study F Sacher, V Probst, Y Iesaka, P Jacon, J Laborderie, F Mizon-Gérard, ... Circulation 114 (22), 2317-2324, 2006 | 636* | 2006 |
Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans H Watanabe, TT Koopmann, S Le Scouarnec, T Yang, CR Ingram, ... The Journal of clinical investigation 118 (6), 2260-2268, 2008 | 591 | 2008 |
Long-term prognosis of individuals with right precordial ST-segment–elevation Brugada syndrome L Eckardt, V Probst, JPP Smits, ES Bahr, C Wolpert, R Schimpf, T Wichter, ... Circulation 111 (3), 257-263, 2005 | 588 | 2005 |
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death CR Bezzina, J Barc, Y Mizusawa, CA Remme, JB Gourraud, F Simonet, ... Nature genetics 45 (9), 1044-1049, 2013 | 577 | 2013 |
Novel SCN5A Mutation Leading Either to Isolated Cardiac Conduction Defect or Brugada Syndrome in a Large French Family F Kyndt, V Probst, F Potet, S Demolombe, JC Chevallier, I Baro, ... Circulation 104 (25), 3081-3086, 2001 | 479 | 2001 |
Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non–SCN5A-related patients JPP Smits, L Eckardt, V Probst, CR Bezzina, JJ Schott, CA Remme, ... Journal of the American College of Cardiology 40 (2), 350-356, 2002 | 469 | 2002 |
Drugs and Brugada syndrome patients: review of the literature, recommendations, and an up-to-date website (www. brugadadrugs. org) PG Postema, C Wolpert, AS Amin, V Probst, M Borggrefe, DM Roden, ... Heart Rhythm 6 (9), 1335-1341, 2009 | 427 | 2009 |
Mitral valve disease—morphology and mechanisms RA Levine, AA Hagége, DP Judge, M Padala, JP Dal-Bianco, E Aikawa, ... Nature reviews cardiology 12 (12), 689-710, 2015 | 412 | 2015 |
Characteristics of recurrent ventricular fibrillation associated with inferolateral early repolarization: role of drug therapy M Haïssaguerre, F Sacher, A Nogami, N Komiya, A Bernard, V Probst, ... Journal of the American College of Cardiology 53 (7), 612-619, 2009 | 411 | 2009 |
Ventricular Fibrillation with Prominent Early Repolarization Associated with a Rare Variant of KCNJ8/KATP Channel M Haïssaguerre, S Chatel, F Sacher, R Weerasooriya, V Probst, ... Journal of cardiovascular electrophysiology 20 (1), 93-98, 2009 | 380 | 2009 |
Clinical aspects and prognosis of Brugada syndrome in children V Probst, I Denjoy, PG Meregalli, JC Amirault, F Sacher, J Mansourati, ... Circulation 115 (15), 2042-2048, 2007 | 371 | 2007 |
Long-term follow-up of patients with short QT syndrome C Giustetto, R Schimpf, A Mazzanti, C Scrocco, P Maury, O Anttonen, ... Journal of the American College of Cardiology 58 (6), 587-595, 2011 | 355 | 2011 |
KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron H Louis-Dit-Picard, J Barc, D Trujillano, S Miserey-Lenkei, N Bouatia-Naji, ... Nature genetics 44 (4), 456-460, 2012 | 349 | 2012 |
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