Denjoy I - Search Results

1

A truncating SCN5A mutation combined with genetic variability causes sick sinus syndrome and early atrial fibrillation.

Ziyadeh-Isleem A, Clatot J, Duchatelet S, Gandjbakhch E, Denjoy I, Hidden-Lucet F, Hatem S, Deschênes I, Coulombe A, Neyroud N, Guicheney P. Ziyadeh-Isleem A, et al. Among authors: denjoy i. Heart Rhythm. 2014 Jun;11(6):1015-1023. doi: 10.1016/j.hrthm.2014.02.021. Epub 2014 Feb 25. Heart Rhythm. 2014. PMID: 24582607 Free PMC article.

2

Readjusting the localization of long QT syndrome gene on chromosome 11p15.

Dausse E, Denjoy I, Kahlem P, Bennaceur M, Fauré S, Weissenbach J, Coumel P, Schwartz K, Guicheney P. Dausse E, et al. Among authors: denjoy i. C R Acad Sci III. 1995 Aug;318(8):879-85. C R Acad Sci III. 1995. PMID: 7583778

3

[Dynamics of ventricular repolarisation].

Leenhardt A, Maison-Blanche P, Denjoy I, Neyroud N, Pellerin D, Catuli D, Thomas O, Coumel P. Leenhardt A, et al. Among authors: denjoy i. Arch Mal Coeur Vaiss. 1995 Dec;88 Spec No 5:27-33. Arch Mal Coeur Vaiss. 1995. PMID: 8729297 French.

4

A mutation in HERG associated with notched T waves in long QT syndrome.

Dausse E, Berthet M, Denjoy I, André-Fouet X, Cruaud C, Bennaceur M, Fauré S, Coumel P, Schwartz K, Guicheney P. Dausse E, et al. Among authors: denjoy i. J Mol Cell Cardiol. 1996 Aug;28(8):1609-15. doi: 10.1006/jmcc.1996.0151. J Mol Cell Cardiol. 1996. PMID: 8877771

5

Exclusion of KCNE1 (IsK) as a candidate gene for Jervell and Lange-Nielsen syndrome.

Tesson F, Donger C, Denjoy I, Berthet M, Bennaceur M, Petit C, Coumel P, Schwarts K, Guicheney P. Tesson F, et al. Among authors: denjoy i. J Mol Cell Cardiol. 1996 Sep;28(9):2051-5. doi: 10.1006/jmcc.1996.0198. J Mol Cell Cardiol. 1996. PMID: 8899564

6

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome.

Neyroud N, Tesson F, Denjoy I, Leibovici M, Donger C, Barhanin J, Fauré S, Gary F, Coumel P, Petit C, Schwartz K, Guicheney P. Neyroud N, et al. Among authors: denjoy i. Nat Genet. 1997 Feb;15(2):186-9. doi: 10.1038/ng0297-186. Nat Genet. 1997. PMID: 9020846

7

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

8

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

9

[Congenital long QT syndrome].

Lupoglazoff JM, Denjoy I, Neyroud N, Guicheney P, Casasoprana A, Coumel P. Lupoglazoff JM, et al. Among authors: denjoy i. Presse Med. 1998 Jun 13;27(21):1029-34. Presse Med. 1998. PMID: 9767826 Review. French.

10

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

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