Similar articles for PMID: 16188595

Year	Number of Results
1942	1
1972	1
1975	1
1976	1
1980	1
1983	1
1987	1
1988	1
1999	2
2000	1
2001	2
2002	2
2003	8
2004	4
2005	6
2006	14
2007	12
2008	15
2009	12
2010	19
2011	11
2012	10
2013	10
2014	14
2015	4
2016	9
2017	11
2018	11
2019	7
2020	7
2021	8
2022	4
2023	5
2024	0

1

Congenital atrial standstill associated with coinheritance of a novel SCN5A mutation and connexin 40 polymorphisms.

Makita N, Sasaki K, Groenewegen WA, Yokota T, Yokoshiki H, Murakami T, Tsutsui H. Makita N, et al. Heart Rhythm. 2005 Oct;2(10):1128-34. doi: 10.1016/j.hrthm.2005.06.032. Heart Rhythm. 2005. PMID: 16188595 Free article.

2

A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill.

Groenewegen WA, Firouzi M, Bezzina CR, Vliex S, van Langen IM, Sandkuijl L, Smits JP, Hulsbeek M, Rook MB, Jongsma HJ, Wilde AA. Groenewegen WA, et al. Circ Res. 2003 Jan 10;92(1):14-22. doi: 10.1161/01.res.0000050585.07097.d7. Circ Res. 2003. PMID: 12522116

3

A homozygous SCN5A mutation associated with atrial standstill and sudden death.

Tan RB, Gando I, Bu L, Cecchin F, Coetzee W. Tan RB, et al. Pacing Clin Electrophysiol. 2018 May 21. doi: 10.1111/pace.13386. Online ahead of print. Pacing Clin Electrophysiol. 2018. PMID: 29781517

4

Gain-of-function mutation in SCN5A causes ventricular arrhythmias and early onset atrial fibrillation.

Lieve KV, Verkerk AO, Podliesna S, van der Werf C, Tanck MW, Hofman N, van Bergen PF, Beekman L, Bezzina CR, Wilde AAM, Lodder EM. Lieve KV, et al. Int J Cardiol. 2017 Jun 1;236:187-193. doi: 10.1016/j.ijcard.2017.01.113. Epub 2017 Jan 29. Int J Cardiol. 2017. PMID: 28262340 Free article.

5

A cardiac sodium channel mutation identified in Brugada syndrome associated with atrial standstill.

Takehara N, Makita N, Kawabe J, Sato N, Kawamura Y, Kitabatake A, Kikuchi K. Takehara N, et al. J Intern Med. 2004 Jan;255(1):137-42. doi: 10.1046/j.0954-6820.2003.01247.x. J Intern Med. 2004. PMID: 14687250 Free article.

6

Enhanced fast-inactivated state stability of cardiac sodium channels by a novel voltage sensor SCN5A mutation, R1632C, as a cause of atypical Brugada syndrome.

Nakajima T, Kaneko Y, Saito A, Ota M, Iijima T, Kurabayashi M. Nakajima T, et al. Heart Rhythm. 2015 Nov;12(11):2296-304. doi: 10.1016/j.hrthm.2015.05.032. Epub 2015 May 29. Heart Rhythm. 2015. PMID: 26031372

7

A novel C-terminal truncation SCN5A mutation from a patient with sick sinus syndrome, conduction disorder and ventricular tachycardia.

Tan BH, Iturralde-Torres P, Medeiros-Domingo A, Nava S, Tester DJ, Valdivia CR, Tusié-Luna T, Ackerman MJ, Makielski JC. Tan BH, et al. Cardiovasc Res. 2007 Dec 1;76(3):409-17. doi: 10.1016/j.cardiores.2007.08.006. Epub 2007 Aug 22. Cardiovasc Res. 2007. PMID: 17897635 Free PMC article.

8

Cardiac sodium channel mutation in atrial fibrillation.

Ellinor PT, Nam EG, Shea MA, Milan DJ, Ruskin JN, MacRae CA. Ellinor PT, et al. Heart Rhythm. 2008 Jan;5(1):99-105. doi: 10.1016/j.hrthm.2007.09.015. Epub 2007 Sep 19. Heart Rhythm. 2008. PMID: 18088563

9

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. 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.

10

SCN5A mutation associated with cardiac conduction defect and atrial arrhythmias.

Laitinen-Forsblom PJ, Mäkynen P, Mäkynen H, Yli-Mäyry S, Virtanen V, Kontula K, Aalto-Setälä K. Laitinen-Forsblom PJ, et al. J Cardiovasc Electrophysiol. 2006 May;17(5):480-5. doi: 10.1111/j.1540-8167.2006.00411.x. J Cardiovasc Electrophysiol. 2006. PMID: 16684018

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