Similar articles for PMID: 10471492

Year	Number of Results
1995	1
1997	1
1998	1
1999	4
2000	8
2001	8
2002	9
2003	13
2004	10
2005	8
2006	5
2007	2
2008	1
2009	1
2010	3
2011	2
2013	1
2014	2
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2017	1
2024	0

1

Cardiac conduction defects associate with mutations in SCN5A.

Schott JJ, Alshinawi C, Kyndt F, Probst V, Hoorntje TM, Hulsbeek M, Wilde AA, Escande D, Mannens MM, Le Marec H. Schott JJ, et al. Nat Genet. 1999 Sep;23(1):20-1. doi: 10.1038/12618. Nat Genet. 1999. PMID: 10471492 No abstract available.

2

Novel Brugada SCN5A mutation causing sudden death in children.

Todd SJ, Campbell MJ, Roden DM, Kannankeril PJ. Todd SJ, et al. Heart Rhythm. 2005 May;2(5):540-3. doi: 10.1016/j.hrthm.2005.01.029. Heart Rhythm. 2005. PMID: 15840483 No abstract available.

3

Clinical and molecular heterogeneity in the Brugada syndrome: a novel gene locus on chromosome 3.

Weiss R, Barmada MM, Nguyen T, Seibel JS, Cavlovich D, Kornblit CA, Angelilli A, Villanueva F, McNamara DM, London B. Weiss R, et al. Circulation. 2002 Feb 12;105(6):707-13. doi: 10.1161/hc0602.103618. Circulation. 2002. PMID: 11839626

4

Novel pore mutation in SCN5A manifests as a spectrum of phenotypes ranging from atrial flutter, conduction disease, and Brugada syndrome to sudden cardiac death.

Rossenbacker T, Carroll SJ, Liu H, Kuipéri C, de Ravel TJ, Devriendt K, Carmeliet P, Kass RS, Heidbüchel H. Rossenbacker T, et al. Heart Rhythm. 2004 Nov;1(5):610-5. doi: 10.1016/j.hrthm.2004.07.001. Heart Rhythm. 2004. PMID: 15851228

5

Genetic analysis of the cardiac sodium channel gene SCN5A in Koreans with Brugada syndrome.

Shin DJ, Jang Y, Park HY, Lee JE, Yang K, Kim E, Bae Y, Kim J, Kim J, Kim SS, Lee MH, Chahine M, Yoon SK. Shin DJ, et al. J Hum Genet. 2004;49(10):573-578. doi: 10.1007/s10038-004-0182-z. Epub 2004 Aug 26. J Hum Genet. 2004. PMID: 15338453

6

p.Y1449C SCN5A mutation associated with overlap disorder comprising conduction disease, Brugada syndrome, and atrial flutter.

Hothi SS, Ara F, Timperley J. Hothi SS, et al. J Cardiovasc Electrophysiol. 2015 Jan;26(1):93-7. doi: 10.1111/jce.12470. Epub 2014 Jul 23. J Cardiovasc Electrophysiol. 2015. PMID: 24903439

7

Genetic analysis of Brugada syndrome in Western Japan: two novel mutations.

Niimura H, Matsunaga A, Kumagai K, Ohwaki K, Ogawa M, Noguchi H, Yonemura K, Saku K. Niimura H, et al. Circ J. 2004 Aug;68(8):740-6. doi: 10.1253/circj.68.740. Circ J. 2004. PMID: 15277732 Free article.

8

Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndrome.

Rook MB, Bezzina Alshinawi C, Groenewegen WA, van Gelder IC, van Ginneken AC, Jongsma HJ, Mannens MM, Wilde AA. Rook MB, et al. Cardiovasc Res. 1999 Dec;44(3):507-17. doi: 10.1016/s0008-6363(99)00350-8. Cardiovasc Res. 1999. PMID: 10690282

9

Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family.

Kyndt F, Probst V, Potet F, Demolombe S, Chevallier JC, Baro I, Moisan JP, Boisseau P, Schott JJ, Escande D, Le Marec H. Kyndt F, et al. Circulation. 2001 Dec 18;104(25):3081-6. doi: 10.1161/hc5001.100834. Circulation. 2001. PMID: 11748104

10

Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non-SCN5A-related patients.

Smits JP, Eckardt L, Probst V, Bezzina CR, Schott JJ, Remme CA, Haverkamp W, Breithardt G, Escande D, Schulze-Bahr E, LeMarec H, Wilde AA. Smits JP, et al. J Am Coll Cardiol. 2002 Jul 17;40(2):350-6. doi: 10.1016/s0735-1097(02)01962-9. J Am Coll Cardiol. 2002. PMID: 12106943 Free article.

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