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Page 1
Parental electrocardiographic screening identifies a high degree of inheritance for congenital and childhood nonimmune isolated atrioventricular block.
Baruteau AE, Behaghel A, Fouchard S, Mabo P, Schott JJ, Dina C, Chatel S, Villain E, Thambo JB, Marçon F, Gournay V, Rouault F, Chantepie A, Guillaumont S, Godart F, Martins RP, Delasalle B, Bonnet C, Fraisse A, Schleich JM, Lusson JR, Dulac Y, Daubert JC, Le Marec H, Probst V. Baruteau AE, et al. Among authors: chatel s. Circulation. 2012 Sep 18;126(12):1469-77. doi: 10.1161/CIRCULATIONAHA.111.069161. Epub 2012 Aug 16. Circulation. 2012. PMID: 22899775 Free article.
Ventricular fibrillation with prominent early repolarization associated with a rare variant of KCNJ8/KATP channel.
Haïssaguerre M, Chatel S, Sacher F, Weerasooriya R, Probst V, Loussouarn G, Horlitz M, Liersch R, Schulze-Bahr E, Wilde A, Kääb S, Koster J, Rudy Y, Le Marec H, Schott JJ. Haïssaguerre M, et al. Among authors: chatel s. J Cardiovasc Electrophysiol. 2009 Jan;20(1):93-8. doi: 10.1111/j.1540-8167.2008.01326.x. J Cardiovasc Electrophysiol. 2009. PMID: 19120683
Identification of large families in early repolarization syndrome.
Gourraud JB, Le Scouarnec S, Sacher F, Chatel S, Derval N, Portero V, Chavernac P, Sandoval JE, Mabo P, Redon R, Schott JJ, Le Marec H, Haïssaguerre M, Probst V. Gourraud JB, et al. Among authors: chatel s. J Am Coll Cardiol. 2013 Jan 15;61(2):164-72. doi: 10.1016/j.jacc.2012.09.040. J Am Coll Cardiol. 2013. PMID: 23273290 Free article.
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
Bezzina CR, Barc J, Mizusawa Y, Remme CA, Gourraud JB, Simonet F, Verkerk AO, Schwartz PJ, Crotti L, Dagradi F, Guicheney P, Fressart V, Leenhardt A, Antzelevitch C, Bartkowiak S, Borggrefe M, Schimpf R, Schulze-Bahr E, Zumhagen S, Behr ER, Bastiaenen R, Tfelt-Hansen J, Olesen MS, Kääb S, Beckmann BM, Weeke P, Watanabe H, Endo N, Minamino T, Horie M, Ohno S, Hasegawa K, Makita N, Nogami A, Shimizu W, Aiba T, Froguel P, Balkau B, Lantieri O, Torchio M, Wiese C, Weber D, Wolswinkel R, Coronel R, Boukens BJ, Bézieau S, Charpentier E, Chatel S, Despres A, Gros F, Kyndt F, Lecointe S, Lindenbaum P, Portero V, Violleau J, Gessler M, Tan HL, Roden DM, Christoffels VM, Le Marec H, Wilde AA, Probst V, Schott JJ, Dina C, Redon R. Bezzina CR, et al. Among authors: chatel s. Nat Genet. 2013 Sep;45(9):1044-9. doi: 10.1038/ng.2712. Epub 2013 Jul 21. Nat Genet. 2013. PMID: 23872634 Free PMC article.
Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome.
Le Scouarnec S, Karakachoff M, Gourraud JB, Lindenbaum P, Bonnaud S, Portero V, Duboscq-Bidot L, Daumy X, Simonet F, Teusan R, Baron E, Violleau J, Persyn E, Bellanger L, Barc J, Chatel S, Martins R, Mabo P, Sacher F, Haïssaguerre M, Kyndt F, Schmitt S, Bézieau S, Le Marec H, Dina C, Schott JJ, Probst V, Redon R. Le Scouarnec S, et al. Among authors: chatel s. Hum Mol Genet. 2015 May 15;24(10):2757-63. doi: 10.1093/hmg/ddv036. Epub 2015 Feb 3. Hum Mol Genet. 2015. PMID: 25650408
Risk Stratification and Therapeutic Approach in Brugada Syndrome.
Probst V, Chatel S, Gourraud JB, Marec HL. Probst V, et al. Among authors: chatel s. Arrhythm Electrophysiol Rev. 2012 Sep;1(1):17-21. doi: 10.15420/aer.2012.1.17. Arrhythm Electrophysiol Rev. 2012. PMID: 26835024 Free PMC article.
Dysfunction of the Voltage-Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome.
Portero V, Le Scouarnec S, Es-Salah-Lamoureux Z, Burel S, Gourraud JB, Bonnaud S, Lindenbaum P, Simonet F, Violleau J, Baron E, Moreau E, Scott C, Chatel S, Loussouarn G, O'Hara T, Mabo P, Dina C, Le Marec H, Schott JJ, Probst V, Baró I, Marionneau C, Charpentier F, Redon R. Portero V, et al. Among authors: chatel s. J Am Heart Assoc. 2016 Jun 10;5(6):e003122. doi: 10.1161/JAHA.115.003122. J Am Heart Assoc. 2016. PMID: 27287695 Free PMC article.
32 results