Probst V - Search Results

1

Genetic association analyses highlight biological pathways underlying mitral valve prolapse.

Dina C, Bouatia-Naji N, Tucker N, Delling FN, Toomer K, Durst R, Perrocheau M, Fernandez-Friera L, Solis J; PROMESA investigators; Le Tourneau T, Chen MH, Probst V, Bosse Y, Pibarot P, Zelenika D, Lathrop M, Hercberg S, Roussel R, Benjamin EJ, Bonnet F, Lo SH, Dolmatova E, Simonet F, Lecointe S, Kyndt F, Redon R, Le Marec H, Froguel P, Ellinor PT, Vasan RS, Bruneval P, Markwald RR, Norris RA, Milan DJ, Slaugenhaupt SA, Levine RA, Schott JJ, Hagege AA; MVP-France; Jeunemaitre X; Leducq Transatlantic MITRAL Network. Dina C, et al. Among authors: probst v. Nat Genet. 2015 Oct;47(10):1206-11. doi: 10.1038/ng.3383. Epub 2015 Aug 24. Nat Genet. 2015. PMID: 26301497 Free PMC article.

2

Cardiac conduction defects associate with mutations in SCN5A.

Schott JJ, Alshinawi C, Kyndt F, Probst V, Hoorntje TM, Hulsbeek M, Wilde AA, Escande D, Mannens MM, Le Marec H. Schott JJ, et al. Among authors: probst v. Nat Genet. 1999 Sep;23(1):20-1. doi: 10.1038/12618. Nat Genet. 1999. PMID: 10471492 No abstract available.

3

Clinical characteristics of a familial inherited myxomatous valvular dystrophy mapped to Xq28.

Trochu JN, Kyndt F, Schott JJ, Gueffet JP, Probst V, Bénichou B, Le Marec H. Trochu JN, et al. Among authors: probst v. J Am Coll Cardiol. 2000 Jun;35(7):1890-7. doi: 10.1016/s0735-1097(00)00617-3. J Am Coll Cardiol. 2000. PMID: 10841240 Free article.

4

Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family.

Kyndt F, Probst V, Potet F, Demolombe S, Chevallier JC, Baro I, Moisan JP, Boisseau P, Schott JJ, Escande D, Le Marec H. Kyndt F, et al. Among authors: probst v. Circulation. 2001 Dec 18;104(25):3081-6. doi: 10.1161/hc5001.100834. Circulation. 2001. PMID: 11748104

5

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.

6

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.

7

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

8

[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.

9

[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.

10

[Prevention of cardiac arrhythmias: what is the place for antiarrhythmic drugs?].

Probst V, Trochu JN, Le Marec H. Probst V, et al. Rev Prat. 2004 Feb 15;54(3):286-90. Rev Prat. 2004. PMID: 15134235 French.

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