Probst V - Search Results

1

Left Ventricular Abnormal Substrate in Brugada Syndrome.

Cheniti G, Haissaguerre M, Dina C, Kamakura T, Duchateau J, Sacher F, Racine HP, Surget E, Simonet F, Gourraud JB, Sridi S, Cochet H, Andre C, Bouyer B, Chauvel R, Tixier R, Derval N, Pambrun T, Dubois R, Jais P, Nademanee K, Redon R, Schott JJ, Probst V, Hocini M, Barc J, Bernus O. Cheniti G, et al. Among authors: probst v. JACC Clin Electrophysiol. 2023 Oct;9(10):2041-2051. doi: 10.1016/j.jacep.2023.05.039. Epub 2023 Jul 19. JACC Clin Electrophysiol. 2023. PMID: 37480873 Free article.

2

Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease.

Probst V, Kyndt F, Potet F, Trochu JN, Mialet G, Demolombe S, Schott JJ, Baró I, Escande D, Le Marec H. Probst V, et al. J Am Coll Cardiol. 2003 Feb 19;41(4):643-52. doi: 10.1016/s0735-1097(02)02864-4. J Am Coll Cardiol. 2003. PMID: 12598077 Free article.

3

Cosegregation of the Marfan syndrome and the long QT syndrome in the same family leads to a severe cardiac phenotype.

Probst V, Allouis M, Kyndt F, Lande G, Trochu JN, Schott JJ, Le Marec H. Probst V, et al. Am J Cardiol. 2003 Mar 1;91(5):635-7. doi: 10.1016/s0002-9149(02)03329-5. Am J Cardiol. 2003. PMID: 12615283 No abstract available.

4

Novel brugada SCN5A mutation leading to ST segment elevation in the inferior or the right precordial leads.

Potet F, Mabo P, Le Coq G, Probst V, Schott JJ, Airaud F, Guihard G, Daubert JC, Escande D, Le Marec H. Potet F, et al. Among authors: probst v. J Cardiovasc Electrophysiol. 2003 Feb;14(2):200-3. doi: 10.1046/j.1540-8167.2003.02382.x. J Cardiovasc Electrophysiol. 2003. PMID: 12693506

5

[Genetics and cardiac arrhythmias].

Probst V, Kyndt F, Allouis M, Schott JJ, Le Marec H. Probst V, et al. Arch Mal Coeur Vaiss. 2003 Nov;96(11):1054-62. Arch Mal Coeur Vaiss. 2003. PMID: 14694781 Review. French.

6

[Genetic aspects of cardiac conduction defects].

Probst V, Kyndt F, Allouis M, Schott JJ, Le Marec H. Probst V, et al. Arch Mal Coeur Vaiss. 2003 Nov;96(11):1067-73. Arch Mal Coeur Vaiss. 2003. PMID: 14694782 Review. French.

7

Unusual clinical presentation in a family with catecholaminergic polymorphic ventricular tachycardia due to a G14876A ryanodine receptor gene mutation.

Allouis M, Probst V, Jaafar P, Schott JJ, Le Marec H. Allouis M, et al. Among authors: probst v. Am J Cardiol. 2005 Mar 1;95(5):700-2. doi: 10.1016/j.amjcard.2004.10.057. Am J Cardiol. 2005. PMID: 15721128

8

Monomorphic ventricular tachycardia due to Brugada syndrome successfully treated by hydroquinidine therapy in a 3-year-old child.

Probst V, Evain S, Gournay V, Marie A, Schott JJ, Boisseau P, LE Marec H. Probst V, et al. J Cardiovasc Electrophysiol. 2006 Jan;17(1):97-100. doi: 10.1111/j.1540-8167.2005.00329.x. J Cardiovasc Electrophysiol. 2006. PMID: 16426410

9

Familial aggregation of calcific aortic valve stenosis in the western part of France.

Probst V, Le Scouarnec S, Legendre A, Jousseaume V, Jaafar P, Nguyen JM, Chaventré A, Le Marec H, Schott JJ. Probst V, et al. Circulation. 2006 Feb 14;113(6):856-60. doi: 10.1161/CIRCULATIONAHA.105.569467. Epub 2006 Feb 6. Circulation. 2006. PMID: 16461814

10

Progressive cardiac conduction defect is the prevailing phenotype in carriers of a Brugada syndrome SCN5A mutation.

Probst V, Allouis M, Sacher F, Pattier S, Babuty D, Mabo P, Mansourati J, Victor J, Nguyen JM, Schott JJ, Boisseau P, Escande D, Le Marec H. Probst V, et al. J Cardiovasc Electrophysiol. 2006 Mar;17(3):270-5. doi: 10.1111/j.1540-8167.2006.00349.x. J Cardiovasc Electrophysiol. 2006. PMID: 16643399

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