Similar articles for PMID: 12123767

Year	Number of Results
1995	2
1996	2
1997	1
1998	4
1999	1
2000	7
2001	7
2002	5
2003	10
2004	7
2005	1
2006	9
2007	11
2008	10
2009	5
2010	7
2011	6
2012	8
2013	6
2014	10
2015	4
2016	8
2017	4
2018	8
2019	6
2020	7
2021	11
2022	7
2023	2
2024	0

1

A novel SCN5A arrhythmia mutation, M1766L, with expression defect rescued by mexiletine.

Valdivia CR, Ackerman MJ, Tester DJ, Wada T, McCormack J, Ye B, Makielski JC. Valdivia CR, et al. Cardiovasc Res. 2002 Aug 1;55(2):279-89. doi: 10.1016/s0008-6363(02)00445-5. Cardiovasc Res. 2002. PMID: 12123767

2

Malignant perinatal variant of long-QT syndrome caused by a profoundly dysfunctional cardiac sodium channel.

Wang DW, Crotti L, Shimizu W, Pedrazzini M, Cantu F, De Filippo P, Kishiki K, Miyazaki A, Ikeda T, Schwartz PJ, George AL Jr. Wang DW, et al. Circ Arrhythm Electrophysiol. 2008 Dec;1(5):370-8. doi: 10.1161/CIRCEP.108.788349. Epub 2008 Dec 2. Circ Arrhythm Electrophysiol. 2008. PMID: 19808432 Free PMC article.

3

Mexiletine rescues a mixed biophysical phenotype of the cardiac sodium channel arising from the SCN5A mutation, N406K, found in LQT3 patients.

Hu RM, Tester DJ, Li R, Sun T, Peterson BZ, Ackerman MJ, Makielski JC, Tan BH. Hu RM, et al. Channels (Austin). 2018;12(1):176-186. doi: 10.1080/19336950.2018.1475794. Channels (Austin). 2018. PMID: 29983085 Free PMC article.

4

Trafficking defects and gating abnormalities of a novel SCN5A mutation question gene-specific therapy in long QT syndrome type 3.

Ruan Y, Denegri M, Liu N, Bachetti T, Seregni M, Morotti S, Severi S, Napolitano C, Priori SG. Ruan Y, et al. Circ Res. 2010 Apr 30;106(8):1374-83. doi: 10.1161/CIRCRESAHA.110.218891. Epub 2010 Mar 25. Circ Res. 2010. PMID: 20339117

5

Effect of pacing and mexiletine on dispersion of repolarisation and arrhythmias in DeltaKPQ SCN5A (long QT3) mice.

Fabritz L, Kirchhof P, Franz MR, Nuyens D, Rossenbacker T, Ottenhof A, Haverkamp W, Breithardt G, Carmeliet E, Carmeliet P. Fabritz L, et al. Cardiovasc Res. 2003 Mar 15;57(4):1085-93. doi: 10.1016/s0008-6363(02)00839-8. Cardiovasc Res. 2003. PMID: 12650887

6

Normalization of ventricular repolarization with flecainide in long QT syndrome patients with SCN5A:DeltaKPQ mutation.

Windle JR, Geletka RC, Moss AJ, Zareba W, Atkins DL. Windle JR, et al. Ann Noninvasive Electrocardiol. 2001 Apr;6(2):153-8. doi: 10.1111/j.1542-474x.2001.tb00100.x. Ann Noninvasive Electrocardiol. 2001. PMID: 11333173 Free PMC article. Clinical Trial.

7

A sodium channel pore mutation causing Brugada syndrome.

Pfahnl AE, Viswanathan PC, Weiss R, Shang LL, Sanyal S, Shusterman V, Kornblit C, London B, Dudley SC Jr. Pfahnl AE, et al. Heart Rhythm. 2007 Jan;4(1):46-53. doi: 10.1016/j.hrthm.2006.09.031. Epub 2006 Sep 28. Heart Rhythm. 2007. PMID: 17198989 Free PMC article.

8

A distinct molecular mechanism by which phenytoin rescues a novel long QT 3 variant.

Gando I, Campana C, Tan RB, Cecchin F, Sobie EA, Coetzee WA. Gando I, et al. J Mol Cell Cardiol. 2020 Jul;144:1-11. doi: 10.1016/j.yjmcc.2020.04.027. Epub 2020 Apr 24. J Mol Cell Cardiol. 2020. PMID: 32339567 Free PMC article.

9

Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome.

Ackerman MJ, Siu BL, Sturner WQ, Tester DJ, Valdivia CR, Makielski JC, Towbin JA. Ackerman MJ, et al. JAMA. 2001 Nov 14;286(18):2264-9. doi: 10.1001/jama.286.18.2264. JAMA. 2001. PMID: 11710892

10

Predicting Patient Response to the Antiarrhythmic Mexiletine Based on Genetic Variation.

Zhu W, Mazzanti A, Voelker TL, Hou P, Moreno JD, Angsutararux P, Naegle KM, Priori SG, Silva JR. Zhu W, et al. Circ Res. 2019 Feb 15;124(4):539-552. doi: 10.1161/CIRCRESAHA.118.314050. Circ Res. 2019. PMID: 30566038 Free PMC article. Clinical Trial.

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