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Items: 1 to 20 of 28

1.

Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system.

Bezzina CR, Rook MB, Groenewegen WA, Herfst LJ, van der Wal AC, Lam J, Jongsma HJ, Wilde AA, Mannens MM.

Circ Res. 2003 Feb 7;92(2):159-68.

2.

The implications of genetic mutations in the sodium channel gene (SCN5A).

Moric E, Herbert E, Trusz-Gluza M, Filipecki A, Mazurek U, Wilczok T.

Europace. 2003 Oct;5(4):325-34. Review.

3.

Molecular basis of isolated cardiac conduction disease.

Viswanathan PC, Balser JR.

Handb Exp Pharmacol. 2006;(171):331-47. Review.

PMID:
16610351
4.

Sodium channel mutations and arrhythmias.

Ruan Y, Liu N, Priori SG.

Nat Rev Cardiol. 2009 May;6(5):337-48. doi: 10.1038/nrcardio.2009.44. Review.

PMID:
19377496
5.

Molecular biology of sodium channels and their role in cardiac arrhythmias.

Grant AO.

Am J Med. 2001 Mar;110(4):296-305. Review.

PMID:
11239848
6.

Genetic mutations and arrhythmia: simulation from DNA to electrocardiogram.

Zhu ZI, Clancy CE.

J Electrocardiol. 2007 Nov-Dec;40(6 Suppl):S47-50. Review.

PMID:
17993328
7.
8.

Sudden cardiac death and inherited arrhythmia syndromes.

Sarkozy A, Brugada P.

J Cardiovasc Electrophysiol. 2005 Sep;16 Suppl 1:S8-20. Review.

PMID:
16138889
9.

Inherited conduction system abnormalities--one group of diseases, many genes.

Wolf CM, Berul CI.

J Cardiovasc Electrophysiol. 2006 Apr;17(4):446-55. Review.

PMID:
16643374
10.

Inherited sodium channelopathies: a continuum of channel dysfunction.

Viswanathan PC, Balser JR.

Trends Cardiovasc Med. 2004 Jan;14(1):28-35. Review.

PMID:
14720472
11.

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. Review.

PMID:
19027780
12.

Cardiac sodium channel Na(v)1.5 and interacting proteins: Physiology and pathophysiology.

Abriel H.

J Mol Cell Cardiol. 2010 Jan;48(1):2-11. doi: 10.1016/j.yjmcc.2009.08.025. Review.

PMID:
19744495
13.

Sodium channel (dys)function and cardiac arrhythmias.

Remme CA, Bezzina CR.

Cardiovasc Ther. 2010 Oct;28(5):287-94. doi: 10.1111/j.1755-5922.2010.00210.x. Review.

PMID:
20645984
14.

Novel mutations in epithelial sodium channel (ENaC) subunit genes and phenotypic expression of multisystem pseudohypoaldosteronism.

Edelheit O, Hanukoglu I, Gizewska M, Kandemir N, Tenenbaum-Rakover Y, Yurdakök M, Zajaczek S, Hanukoglu A.

Clin Endocrinol (Oxf). 2005 May;62(5):547-53. Review.

PMID:
15853823
15.

Molecular genetics of arrhythmias--a new paradigm.

Schulze-Bahr E, Haverkamp W, Borggrefe M, Wedekind H, Mönnig G, Mergenthaler J, Assmann G, Funke H, Breithardt G.

Z Kardiol. 2000;89 Suppl 4:IV12-22. Review.

PMID:
10810773
16.

Phenotypical manifestations of mutations in the genes encoding subunits of the cardiac sodium channel.

Wilde AA, Brugada R.

Circ Res. 2011 Apr 1;108(7):884-97. doi: 10.1161/CIRCRESAHA.110.238469. Review.

17.

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. Review.

PMID:
19041666
18.

Sodium channel variants in heart disease: expanding horizons.

Tan HL.

J Cardiovasc Electrophysiol. 2006 May;17 Suppl 1:S151-S157. Review.

PMID:
16686672
19.

Trafficking and functional expression of cardiac Na+ channels.

Herfst LJ, Rook MB, Jongsma HJ.

J Mol Cell Cardiol. 2004 Feb;36(2):185-93. Review.

PMID:
14871545
20.

Inherited progressive cardiac conduction disorders.

Baruteau AE, Probst V, Abriel H.

Curr Opin Cardiol. 2015 Jan;30(1):33-9. doi: 10.1097/HCO.0000000000000134. Review.

PMID:
25426816
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