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Page 1
[Brugada syndrome].
Denjoy I, Extramiana F, Lupoglazoff JM, Leenhardt A. Denjoy I, et al. Among authors: lupoglazoff jm. Presse Med. 2007 Jul-Aug;36(7-8):1109-16. doi: 10.1016/j.lpm.2007.03.019. Epub 2007 Apr 18. Presse Med. 2007. PMID: 17446038 Review. French.
[Congenital long QT syndrome].
Lupoglazoff JM, Denjoy I, Neyroud N, Guicheney P, Casasoprana A, Coumel P. Lupoglazoff JM, et al. Presse Med. 1998 Jun 13;27(21):1029-34. Presse Med. 1998. PMID: 9767826 Review. French.
Arrhythmic sudden death in children.
Denjoy I, Lupoglazoff JM, Guicheney P, Leenhardt A. Denjoy I, et al. Among authors: lupoglazoff jm. Arch Cardiovasc Dis. 2008 Feb;101(2):121-5. doi: 10.1016/s1875-2136(08)70269-9. Arch Cardiovasc Dis. 2008. PMID: 18398397 Free article. Review.
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: lupoglazoff jm. Circulation. 2007 Apr 17;115(15):2042-8. doi: 10.1161/CIRCULATIONAHA.106.664219. Epub 2007 Apr 2. Circulation. 2007. PMID: 17404158
Incidence and risk factors of arrhythmic events in catecholaminergic polymorphic ventricular tachycardia.
Hayashi M, Denjoy I, Extramiana F, Maltret A, Buisson NR, Lupoglazoff JM, Klug D, Hayashi M, Takatsuki S, Villain E, Kamblock J, Messali A, Guicheney P, Lunardi J, Leenhardt A. Hayashi M, et al. Among authors: lupoglazoff jm. Circulation. 2009 May 12;119(18):2426-34. doi: 10.1161/CIRCULATIONAHA.108.829267. Epub 2009 Apr 27. Circulation. 2009. PMID: 19398665 Free article.
The role of stress test for predicting genetic mutations and future cardiac events in asymptomatic relatives of catecholaminergic polymorphic ventricular tachycardia probands.
Hayashi M, Denjoy I, Hayashi M, Extramiana F, Maltret A, Roux-Buisson N, Lupoglazoff JM, Klug D, Maury P, Messali A, Guicheney P, Leenhardt A. Hayashi M, et al. Among authors: lupoglazoff jm. Europace. 2012 Sep;14(9):1344-51. doi: 10.1093/europace/eus031. Epub 2012 Mar 1. Europace. 2012. PMID: 22383456
SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroups.
Baruteau AE, Kyndt F, Behr ER, Vink AS, Lachaud M, Joong A, Schott JJ, Horie M, Denjoy I, Crotti L, Shimizu W, Bos JM, Stephenson EA, Wong L, Abrams DJ, Davis AM, Winbo A, Dubin AM, Sanatani S, Liberman L, Kaski JP, Rudic B, Kwok SY, Rieubland C, Tfelt-Hansen J, Van Hare GF, Guyomarc'h-Delasalle B, Blom NA, Wijeyeratne YD, Gourraud JB, Le Marec H, Ozawa J, Fressart V, Lupoglazoff JM, Dagradi F, Spazzolini C, Aiba T, Tester DJ, Zahavich LA, Beauséjour-Ladouceur V, Jadhav M, Skinner JR, Franciosi S, Krahn AD, Abdelsayed M, Ruben PC, Yung TC, Ackerman MJ, Wilde AA, Schwartz PJ, Probst V. Baruteau AE, et al. Among authors: lupoglazoff jm. Eur Heart J. 2018 Aug 14;39(31):2879-2887. doi: 10.1093/eurheartj/ehy412. Eur Heart J. 2018. PMID: 30059973 Free article.
[Congenital long QT syndrome].
Lupoglazoff JM, Denjoy I, Guicheney P, Casasoprana A, Coumel P. Lupoglazoff JM, et al. Arch Pediatr. 2001 May;8(5):525-34. doi: 10.1016/s0929-693x(00)00261-x. Arch Pediatr. 2001. PMID: 11396115 Review. French.
61 results