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Page 1
SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndrome.
Probst V, Wilde AA, Barc J, Sacher F, Babuty D, Mabo P, Mansourati J, Le Scouarnec S, Kyndt F, Le Caignec C, Guicheney P, Gouas L, Albuisson J, Meregalli PG, Le Marec H, Tan HL, Schott JJ. Probst V, et al. Among authors: babuty d. Circ Cardiovasc Genet. 2009 Dec;2(6):552-7. doi: 10.1161/CIRCGENETICS.109.853374. Epub 2009 Sep 29. Circ Cardiovasc Genet. 2009. PMID: 20031634
Outcome after implantation of a cardioverter-defibrillator in patients with Brugada syndrome: a multicenter study.
Sacher F, Probst V, Iesaka Y, Jacon P, Laborderie J, Mizon-Gérard F, Mabo P, Reuter S, Lamaison D, Takahashi Y, O'Neill MD, Garrigue S, Pierre B, Jaïs P, Pasquié JL, Hocini M, Salvador-Mazenq M, Nogami A, Amiel A, Defaye P, Bordachar P, Boveda S, Maury P, Klug D, Babuty D, Haïssaguerre M, Mansourati J, Clémenty J, Le Marec H. Sacher F, et al. Among authors: babuty d. Circulation. 2006 Nov 28;114(22):2317-24. doi: 10.1161/CIRCULATIONAHA.106.628537. Epub 2006 Nov 20. Circulation. 2006. PMID: 17116772
Clinical aspects and prognosis of Brugada syndrome in children.
Probst V, Denjoy I, Meregalli PG, Amirault JC, Sacher F, Mansourati J, Babuty D, Villain E, Victor J, Schott JJ, Lupoglazoff JM, Mabo P, Veltmann C, Jesel L, Chevalier P, Clur SA, Haissaguerre M, Wolpert C, Le Marec H, Wilde AA. Probst V, et al. Among authors: babuty d. Circulation. 2007 Apr 17;115(15):2042-8. doi: 10.1161/CIRCULATIONAHA.106.664219. Epub 2007 Apr 2. Circulation. 2007. PMID: 17404158
Are women with severely symptomatic brugada syndrome different from men?
Sacher F, Meregalli P, Veltmann C, Field ME, Solnon A, Bru P, Abbey S, Jaïs P, Tan HL, Wolpert C, Lande G, Bertault V, Derval N, Babuty D, Lacroix D, Boveda S, Maury P, Hocini M, Clémenty J, Mabo P, Lemarec H, Mansourati J, Borggrefe M, Wilde A, Haïssaguerre M, Probst V. Sacher F, et al. Among authors: babuty d. J Cardiovasc Electrophysiol. 2008 Nov;19(11):1181-5. doi: 10.1111/j.1540-8167.2008.01223.x. Epub 2008 May 19. J Cardiovasc Electrophysiol. 2008. PMID: 18554195
Sodium-channel blocker challenge in the familial screening of Brugada syndrome: Safety and predictors of positivity.
Therasse D, Sacher F, Petit B, Babuty D, Mabo P, Martins R, Jesel L, Maury P, Pasquie JL, Mansourati J, Dupuis JM, Kyndt F, Thollet A, Guyomarch B, Barc J, Schott JJ, Le Marec H, Redon R, Probst V, Gourraud JB. Therasse D, et al. Among authors: babuty d. Heart Rhythm. 2017 Oct;14(10):1442-1448. doi: 10.1016/j.hrthm.2017.06.031. Epub 2017 Jun 27. Heart Rhythm. 2017. PMID: 28666944
Value of the sodium-channel blocker challenge in Brugada syndrome.
Therasse D, Sacher F, Babuty D, Mabo P, Mansourati J, Kyndt F, Redon R, Schott JJ, Barc J, Probst V, Gourraud JB. Therasse D, et al. Among authors: babuty d. Int J Cardiol. 2017 Oct 15;245:178-180. doi: 10.1016/j.ijcard.2017.05.099. Epub 2017 Aug 4. Int J Cardiol. 2017. PMID: 28784436
Clinical presentation and follow-up of women affected by Brugada syndrome.
Berthome P, Tixier R, Briand J, Geoffroy O, Babuty D, Mansourati J, Jesel L, Dupuis JM, Bru P, Kyndt F, Guyomarch B, Thollet A, Behar N, Mabo P, Sacher F, Probst V, Gourraud JB. Berthome P, et al. Among authors: babuty d. Heart Rhythm. 2019 Feb;16(2):260-267. doi: 10.1016/j.hrthm.2018.08.032. Epub 2018 Sep 5. Heart Rhythm. 2019. PMID: 30193851
Number of electrocardiogram leads in the diagnosis of spontaneous Brugada syndrome.
Arnaud M, Berthome P, Tixier R, Briand J, Geoffroy O, Le Guillou X, Babuty D, Mansourati J, Jesel L, Dupuis JM, Bru P, Kyndt F, Guyomarch B, Thollet A, Behar N, Mabo P, Sacher F, Probst V, Gourraud JB. Arnaud M, et al. Among authors: babuty d. Arch Cardiovasc Dis. 2020 Mar;113(3):152-158. doi: 10.1016/j.acvd.2019.10.007. Epub 2019 Nov 29. Arch Cardiovasc Dis. 2020. PMID: 31787523 Free article.
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.
Barc J, Tadros R, Glinge C, Chiang DY, Jouni M, Simonet F, Jurgens SJ, Baudic M, Nicastro M, Potet F, Offerhaus JA, Walsh R, Choi SH, Verkerk AO, Mizusawa Y, Anys S, Minois D, Arnaud M, Duchateau J, Wijeyeratne YD, Muir A, Papadakis M, Castelletti S, Torchio M, Ortuño CG, Lacunza J, Giachino DF, Cerrato N, Martins RP, Campuzano O, Van Dooren S, Thollet A, Kyndt F, Mazzanti A, Clémenty N, Bisson A, Corveleyn A, Stallmeyer B, Dittmann S, Saenen J, Noël A, Honarbakhsh S, Rudic B, Marzak H, Rowe MK, Federspiel C, Le Page S, Placide L, Milhem A, Barajas-Martinez H, Beckmann BM, Krapels IP, Steinfurt J, Winkel BG, Jabbari R, Shoemaker MB, Boukens BJ, Škorić-Milosavljević D, Bikker H, Manevy F, Lichtner P, Ribasés M, Meitinger T, Müller-Nurasyid M; KORA-Study Group; Veldink JH, van den Berg LH, Van Damme P, Cusi D, Lanzani C, Rigade S, Charpentier E, Baron E, Bonnaud S, Lecointe S, Donnart A, Le Marec H, Chatel S, Karakachoff M, Bézieau S, London B, Tfelt-Hansen J, Roden D, Odening KE, Cerrone M, Chinitz LA, Volders PG, van de Berg MP, Laurent G, Faivre L, Antzelevitch C, Kääb S, Arnaout AA, Dupuis JM, Pasquie JL, Billon O, Roberts JD, Jesel L, Borggrefe M, Lambiase PD, Mansourati J, Loe… See abstract for full author list ➔ Barc J, et al. Among authors: babuty d. Nat Genet. 2022 Mar;54(3):232-239. doi: 10.1038/s41588-021-01007-6. Epub 2022 Feb 24. Nat Genet. 2022. PMID: 35210625 Free PMC article.
286 results