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vincent probst
vincent probst
université de nantes
Verified email at chu-nantes.fr
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Cited by
Cited by
Year
Heart disease and stroke statistics—2017 update: a report from the American Heart Association
EJ Benjamin, MJ Blaha, SE Chiuve, M Cushman, SR Das, R Deo, ...
circulation 135 (10), e146-e603, 2017
168392017
Sudden cardiac arrest associated with early repolarization
M Haïssaguerre, N Derval, F Sacher, L Jesel, I Deisenhofer, L de Roy, ...
New England Journal of Medicine 358 (19), 2016-2023, 2008
18312008
2018 ESC Guidelines for the diagnosis and management of syncope
M Brignole, A Moya, FJ De Lange, JC Deharo, PM Elliott, A Fanciulli, ...
Polish Heart Journal (Kardiologia Polska) 76 (8), 1119-1198, 2018
18232018
Long-term prognosis of patients diagnosed with Brugada syndrome: results from the FINGER Brugada Syndrome Registry
V Probst, C Veltmann, L Eckardt, PG Meregalli, F Gaita, HL Tan, D Babuty, ...
Circulation 121 (5), 635-643, 2010
9272010
An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing
JD Kapplinger, DJ Tester, M Alders, B Benito, M Berthet, J Brugada, ...
Heart rhythm 7 (1), 33-46, 2010
7892010
Cardiac conduction defects associate with mutations in SCN5A
JJ Schott, C Alshinawi, F Kyndt, V Probst, TM Hoorntje, M Hulsbeek, ...
Nature genetics 23 (1), 20-21, 1999
7831999
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
609*2006
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
5752005
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
5742008
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
5342013
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
4722001
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
4522002
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
3992009
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
3972009
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
3772015
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
3742009
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
3532007
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
3332011
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
3312012
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
DE Arking, SL Pulit, L Crotti, P Van Der Harst, PB Munroe, TT Koopmann, ...
Nature genetics 46 (8), 826-836, 2014
3202014
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