Similar articles for PMID: 11823453

Year	Number of Results
1990	1
1995	1
1998	3
1999	7
2000	9
2001	8
2002	8
2003	9
2004	11
2005	11
2006	9
2007	12
2008	8
2009	8
2010	7
2011	5
2012	4
2013	8
2014	6
2015	4
2016	11
2017	9
2018	8
2019	6
2021	3
2022	4
2023	1
2024	0

1

Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome.

Vatta M, Dumaine R, Varghese G, Richard TA, Shimizu W, Aihara N, Nademanee K, Brugada R, Brugada J, Veerakul G, Li H, Bowles NE, Brugada P, Antzelevitch C, Towbin JA. Vatta M, et al. Hum Mol Genet. 2002 Feb 1;11(3):337-45. doi: 10.1093/hmg/11.3.337. Hum Mol Genet. 2002. PMID: 11823453

2

Novel mutations in domain I of SCN5A cause Brugada syndrome.

Vatta M, Dumaine R, Antzelevitch C, Brugada R, Li H, Bowles NE, Nademanee K, Brugada J, Brugada P, Towbin JA. Vatta M, et al. Mol Genet Metab. 2002 Apr;75(4):317-24. doi: 10.1016/S1096-7192(02)00006-9. Mol Genet Metab. 2002. PMID: 12051963

3

Is sudden unexplained nocturnal death syndrome in Southern China a cardiac sodium channel dysfunction disorder?

Liu C, Tester DJ, Hou Y, Wang W, Lv G, Ackerman MJ, Makielski JC, Cheng J. Liu C, et al. Forensic Sci Int. 2014 Mar;236:38-45. doi: 10.1016/j.forsciint.2013.12.033. Epub 2014 Jan 7. Forensic Sci Int. 2014. PMID: 24529773

4

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.

5

The biophysical characterization of the first SCN5A mutation R1512W identified in Chinese sudden unexplained nocturnal death syndrome.

Zheng J, Zhou F, Su T, Huang L, Wu Y, Yin K, Wu Q, Tang S, Makielski JC, Cheng J. Zheng J, et al. Medicine (Baltimore). 2016 Jun;95(23):e3836. doi: 10.1097/MD.0000000000003836. Medicine (Baltimore). 2016. PMID: 27281089 Free PMC article.

6

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

7

Brugada syndrome and fever: genetic and molecular characterization of patients carrying SCN5A mutations.

Keller DI, Rougier JS, Kucera JP, Benammar N, Fressart V, Guicheney P, Madle A, Fromer M, Schläpfer J, Abriel H. Keller DI, et al. Cardiovasc Res. 2005 Aug 15;67(3):510-9. doi: 10.1016/j.cardiores.2005.03.024. Cardiovasc Res. 2005. PMID: 15890323 Free article.

8

Electrophysiological characterization of SCN5A mutations causing long QT (E1784K) and Brugada (R1512W and R1432G) syndromes.

Deschênes I, Baroudi G, Berthet M, Barde I, Chalvidan T, Denjoy I, Guicheney P, Chahine M. Deschênes I, et al. Cardiovasc Res. 2000 Apr;46(1):55-65. doi: 10.1016/s0008-6363(00)00006-7. Cardiovasc Res. 2000. PMID: 10727653

9

Distinct functional defect of three novel Brugada syndrome related cardiac sodium channel mutations.

Hsueh CH, Chen WP, Lin JL, Tsai CT, Liu YB, Juang JM, Tsao HM, Su MJ, Lai LP. Hsueh CH, et al. J Biomed Sci. 2009 Feb 20;16(1):23. doi: 10.1186/1423-0127-16-23. J Biomed Sci. 2009. PMID: 19272188 Free PMC article.

10

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

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