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Results: 12

Related Articles by Review for PubMed (Select 23538271)

1.

Coexistence of epilepsy and Brugada syndrome in a family with SCN5A mutation.

Parisi P, Oliva A, Coll Vidal M, Partemi S, Campuzano O, Iglesias A, Pisani D, Pascali VL, Paolino MC, Villa MP, Zara F, Tassinari CA, Striano P, Brugada R.

Epilepsy Res. 2013 Aug;105(3):415-8. doi: 10.1016/j.eplepsyres.2013.02.024. Epub 2013 Mar 25.

PMID:
23538271
2.

Cardiac sodium channelopathy associated with SCN5A mutations: electrophysiological, molecular and genetic aspects.

Remme CA.

J Physiol. 2013 Sep 1;591(Pt 17):4099-116. doi: 10.1113/jphysiol.2013.256461. Epub 2013 Jul 1. Review.

3.

[Cardiac sodium channelopathy from bench to bedside].

Zhang YM, Zhou N.

Zhonghua Er Ke Za Zhi. 2013 Nov;51(11):874-7. Review. Chinese. No abstract available.

PMID:
24484568
4.

Cardiac sodium channel overlap syndromes: different faces of SCN5A mutations.

Remme CA, Wilde AA, Bezzina CR.

Trends Cardiovasc Med. 2008 Apr;18(3):78-87. doi: 10.1016/j.tcm.2008.01.002. Review.

PMID:
18436145
5.

Genetics of Brugada syndrome.

Campuzano O, Brugada R, Iglesias A.

Curr Opin Cardiol. 2010 May;25(3):210-5. doi: 10.1097/HCO.0b013e32833846ee. Review.

PMID:
20224390
6.

Cardiac sodium channelopathies.

Amin AS, Asghari-Roodsari A, Tan HL.

Pflugers Arch. 2010 Jul;460(2):223-37. doi: 10.1007/s00424-009-0761-0. Epub 2009 Nov 29. Review.

7.

Brugada syndrome: two decades of progress.

Veerakul G, Nademanee K.

Circ J. 2012;76(12):2713-22. Epub 2012 Nov 14. Review.

8.

SCN5A channelopathies--an update on mutations and mechanisms.

Zimmer T, Surber R.

Prog Biophys Mol Biol. 2008 Oct-Nov;98(2-3):120-36. doi: 10.1016/j.pbiomolbio.2008.10.005. Epub 2008 Nov 5. Review.

PMID:
19027780
9.

Channelopathies from mutations in the cardiac sodium channel protein complex.

Adsit GS, Vaidyanathan R, Galler CM, Kyle JW, Makielski JC.

J Mol Cell Cardiol. 2013 Aug;61:34-43. doi: 10.1016/j.yjmcc.2013.03.017. Epub 2013 Apr 1. Review.

10.

Mouse models of SCN5A-related cardiac arrhythmias.

Charpentier F, Bourgé A, Mérot J.

Prog Biophys Mol Biol. 2008 Oct-Nov;98(2-3):230-7. doi: 10.1016/j.pbiomolbio.2008.10.012. Epub 2008 Nov 12. Review.

PMID:
19041666
11.

Genetic biomarkers in Brugada syndrome.

Li A, Saba MM, Behr ER.

Biomark Med. 2013 Aug;7(4):535-46. doi: 10.2217/bmm.13.78. Review.

PMID:
23905889
12.

Channelopathies as a genetic cause of epilepsy.

Mulley JC, Scheffer IE, Petrou S, Berkovic SF.

Curr Opin Neurol. 2003 Apr;16(2):171-6. Review.

PMID:
12644745
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