Denjoy I - Search Results

1

Mutation location and IKs regulation in the arrhythmic risk of long QT syndrome type 1: the importance of the KCNQ1 S6 region.

Schwartz PJ, Moreno C, Kotta MC, Pedrazzini M, Crotti L, Dagradi F, Castelletti S, Haugaa KH, Denjoy I, Shkolnikova MA, Brink PA, Heradien MJ, Seyen SRM, Spätjens RLHMG, Spazzolini C, Volders PGA. Schwartz PJ, et al. Among authors: denjoy i. Eur Heart J. 2021 Dec 7;42(46):4743-4755. doi: 10.1093/eurheartj/ehab582. Eur Heart J. 2021. PMID: 34505893 Free PMC article.

2

KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome.

Donger C, Denjoy I, Berthet M, Neyroud N, Cruaud C, Bennaceur M, Chivoret G, Schwartz K, Coumel P, Guicheney P. Donger C, et al. Among authors: denjoy i. Circulation. 1997 Nov 4;96(9):2778-81. doi: 10.1161/01.cir.96.9.2778. Circulation. 1997. PMID: 9386136

3

Diagnostic performance of QT interval variables from 24-h electrocardiography in the long QT syndrome.

Neyroud N, Maison-Blanche P, Denjoy I, Chevret S, Donger C, Dausse E, Fayn J, Badilini F, Menhabi N, Schwartz K, Guicheney P, Coumel P. Neyroud N, et al. Among authors: denjoy i. Eur Heart J. 1998 Jan;19(1):158-65. doi: 10.1053/euhj.1997.0730. Eur Heart J. 1998. PMID: 9503190

4

Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndrome.

Neyroud N, Denjoy I, Donger C, Gary F, Villain E, Leenhardt A, Benali K, Schwartz K, Coumel P, Guicheney P. Neyroud N, et al. Among authors: denjoy i. Eur J Hum Genet. 1998 Mar-Apr;6(2):129-33. doi: 10.1038/sj.ejhg.5200165. Eur J Hum Genet. 1998. PMID: 9781056

5

Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome.

Neyroud N, Richard P, Vignier N, Donger C, Denjoy I, Demay L, Shkolnikova M, Pesce R, Chevalier P, Hainque B, Coumel P, Schwartz K, Guicheney P. Neyroud N, et al. Among authors: denjoy i. Circ Res. 1999 Feb 19;84(3):290-7. doi: 10.1161/01.res.84.3.290. Circ Res. 1999. PMID: 10024302

6

Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias.

Schwartz PJ, Priori SG, Spazzolini C, Moss AJ, Vincent GM, Napolitano C, Denjoy I, Guicheney P, Breithardt G, Keating MT, Towbin JA, Beggs AH, Brink P, Wilde AA, Toivonen L, Zareba W, Robinson JL, Timothy KW, Corfield V, Wattanasirichaigoon D, Corbett C, Haverkamp W, Schulze-Bahr E, Lehmann MH, Schwartz K, Coumel P, Bloise R. Schwartz PJ, et al. Among authors: denjoy i. Circulation. 2001 Jan 2;103(1):89-95. doi: 10.1161/01.cir.103.1.89. Circulation. 2001. PMID: 11136691 Clinical Trial.

7

Decreased nocturnal standard deviation of averaged NN intervals. An independent marker to identify patients at risk in the Brugada Syndrome.

Hermida JS, Leenhardt A, Cauchemez B, Denjoy I, Jarry G, Mizon F, Milliez P, Rey JL, Beaufils P, Coumel P. Hermida JS, et al. Among authors: denjoy i. Eur Heart J. 2003 Nov;24(22):2061-9. doi: 10.1016/j.ehj.2003.08.019. Eur Heart J. 2003. PMID: 14613743

8

Low incidence of cardiac events with beta-blocking therapy in children with long QT syndrome.

Villain E, Denjoy I, Lupoglazoff JM, Guicheney P, Hainque B, Lucet V, Bonnet D. Villain E, et al. Among authors: denjoy i. Eur Heart J. 2004 Aug;25(16):1405-11. doi: 10.1016/j.ehj.2004.06.016. Eur Heart J. 2004. PMID: 15321698 Clinical Trial.

9

The Jervell and Lange-Nielsen syndrome: natural history, molecular basis, and clinical outcome.

Schwartz PJ, Spazzolini C, Crotti L, Bathen J, Amlie JP, Timothy K, Shkolnikova M, Berul CI, Bitner-Glindzicz M, Toivonen L, Horie M, Schulze-Bahr E, Denjoy I. Schwartz PJ, et al. Among authors: denjoy i. Circulation. 2006 Feb 14;113(6):783-90. doi: 10.1161/CIRCULATIONAHA.105.592899. Epub 2006 Feb 6. Circulation. 2006. PMID: 16461811

10

[The Jervell and Lange-Nielsen syndrome. Natural history, molecular basis and clinical outcome].

Denjoy I, Lupoglazoff JM, Villain E, Vaksmann G, Godart F, Lucet V, Leenhardt A, Guicheney P, Schwartz P. Denjoy I, et al. Arch Mal Coeur Vaiss. 2007 May;100(5):359-64. Arch Mal Coeur Vaiss. 2007. PMID: 17646758 French.

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