Guicheney P - 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: guicheney p. 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

Dominant-negative effect of SCN5A N-terminal mutations through the interaction of Na(v)1.5 α-subunits.

Clatot J, Ziyadeh-Isleem A, Maugenre S, Denjoy I, Liu H, Dilanian G, Hatem SN, Deschênes I, Coulombe A, Guicheney P, Neyroud N. Clatot J, et al. Among authors: guicheney p. Cardiovasc Res. 2012 Oct 1;96(1):53-63. doi: 10.1093/cvr/cvs211. Epub 2012 Jun 27. Cardiovasc Res. 2012. PMID: 22739120 Free PMC article.

3

R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation.

Bartos DC, Duchatelet S, Burgess DE, Klug D, Denjoy I, Peat R, Lupoglazoff JM, Fressart V, Berthet M, Ackerman MJ, January CT, Guicheney P, Delisle BP. Bartos DC, et al. Among authors: guicheney p. Heart Rhythm. 2011 Jan;8(1):48-55. doi: 10.1016/j.hrthm.2010.09.010. Epub 2010 Sep 17. Heart Rhythm. 2011. PMID: 20850564 Free PMC article.

4

MOG1: a new susceptibility gene for Brugada syndrome.

Kattygnarath D, Maugenre S, Neyroud N, Balse E, Ichai C, Denjoy I, Dilanian G, Martins RP, Fressart V, Berthet M, Schott JJ, Leenhardt A, Probst V, Le Marec H, Hainque B, Coulombe A, Hatem SN, Guicheney P. Kattygnarath D, et al. Among authors: guicheney p. Circ Cardiovasc Genet. 2011 Jun;4(3):261-8. doi: 10.1161/CIRCGENETICS.110.959130. Epub 2011 Mar 29. Circ Cardiovasc Genet. 2011. PMID: 21447824

5

Inter-Regulation of K_v4.3 and Voltage-Gated Sodium Channels Underlies Predisposition to Cardiac and Neuronal Channelopathies.

Clatot J, Neyroud N, Cox R, Souil C, Huang J, Guicheney P, Antzelevitch C. Clatot J, et al. Among authors: guicheney p. Int J Mol Sci. 2020 Jul 17;21(14):5057. doi: 10.3390/ijms21145057. Int J Mol Sci. 2020. PMID: 32709127 Free PMC article.

6

In vivo Dominant-Negative Effect of an SCN5A Brugada Syndrome Variant.

Doisne N, Grauso M, Mougenot N, Clergue M, Souil C, Coulombe A, Guicheney P, Neyroud N. Doisne N, et al. Among authors: guicheney p. Front Physiol. 2021 May 28;12:661413. doi: 10.3389/fphys.2021.661413. eCollection 2021. Front Physiol. 2021. PMID: 34122134 Free PMC article.

7

Trafficking and Gating Cooperation Between Deficient Na_v1.5-mutant Channels to Rescue I_Na.

Clatot J, Coulombe A, Deschênes I, Guicheney P, Neyroud N. Clatot J, et al. Among authors: guicheney p. Front Biosci (Landmark Ed). 2022 Jun 30;27(7):209. doi: 10.31083/j.fbl2707209. Front Biosci (Landmark Ed). 2022. PMID: 35866404 Free article.

8

The occurrence of Brugada syndrome and isolated cardiac conductive disease in the same family could be due to a single SCN5A mutation or to the accidental association of both diseases.

Six I, Hermida JS, Huang H, Gouas L, Fressart V, Benammar N, Hainque B, Denjoy I, Chahine M, Guicheney P. Six I, et al. Among authors: guicheney p. Europace. 2008 Jan;10(1):79-85. doi: 10.1093/europace/eum271. Epub 2007 Dec 21. Europace. 2008. PMID: 18156160

9

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: guicheney p. Eur J Hum Genet. 1998 Mar-Apr;6(2):129-33. doi: 10.1038/sj.ejhg.5200165. Eur J Hum Genet. 1998. PMID: 9781056

10

Novel SCN5A mutations in two families with "Brugada-like" ST elevation in the inferior leads and conduction disturbances.

Maury P, Moreau A, Hidden-Lucet F, Leenhardt A, Fressart V, Berthet M, Denjoy I, Bennamar N, Rollin A, Cardin C, Guicheney P, Chahine M. Maury P, et al. Among authors: guicheney p. J Interv Card Electrophysiol. 2013 Aug;37(2):131-40. doi: 10.1007/s10840-013-9805-7. Epub 2013 Apr 24. J Interv Card Electrophysiol. 2013. PMID: 23612926

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

264 results

Search Page

Filters