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Results: 14

1.

Sudden infant death syndrome-associated mutations in the sodium channel beta subunits.

Tan BH, Pundi KN, Van Norstrand DW, Valdivia CR, Tester DJ, Medeiros-Domingo A, Makielski JC, Ackerman MJ.

Heart Rhythm. 2010 Jun;7(6):771-8. doi: 10.1016/j.hrthm.2010.01.032. Epub 2010 Feb 1.

PMID:
20226894
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Cardiac channelopathies and sudden infant death syndrome.

Tfelt-Hansen J, Winkel BG, Grunnet M, Jespersen T.

Cardiology. 2011;119(1):21-33. doi: 10.1159/000329047. Epub 2011 Jul 16. Review.

PMID:
21778721
[PubMed - indexed for MEDLINE]
3.

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.

PMID:
20091048
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Sudden infant death syndrome: how significant are the cardiac channelopathies?

Tester DJ, Ackerman MJ.

Cardiovasc Res. 2005 Aug 15;67(3):388-96. Review.

PMID:
15913580
[PubMed - indexed for MEDLINE]
Free Article
5.

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.

PMID:
14753626
[PubMed - indexed for MEDLINE]
Free Article
6.

Cardiac ion channel mutations in the sudden infant death syndrome.

Klaver EC, Versluijs GM, Wilders R.

Int J Cardiol. 2011 Oct 20;152(2):162-70. doi: 10.1016/j.ijcard.2010.12.051. Epub 2011 Jan 6. Review.

PMID:
21215473
[PubMed - indexed for MEDLINE]
Free Article
7.

State of postmortem genetic testing known as the cardiac channel molecular autopsy in the forensic evaluation of unexplained sudden cardiac death in the young.

Ackerman MJ.

Pacing Clin Electrophysiol. 2009 Jul;32 Suppl 2:S86-9. doi: 10.1111/j.1540-8159.2009.02393.x. Review.

PMID:
19602172
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

The genetic basis of Brugada syndrome: a mutation update.

Hedley PL, Jørgensen P, Schlamowitz S, Moolman-Smook J, Kanters JK, Corfield VA, Christiansen M.

Hum Mutat. 2009 Sep;30(9):1256-66. doi: 10.1002/humu.21066. Review.

PMID:
19606473
[PubMed - indexed for MEDLINE]
9.

Genetic Na+ channelopathies and sinus node dysfunction.

Lei M, Huang CL, Zhang Y.

Prog Biophys Mol Biol. 2008 Oct-Nov;98(2-3):171-8. doi: 10.1016/j.pbiomolbio.2008.10.003. Epub 2008 Nov 5. Review.

PMID:
19027778
[PubMed - indexed for MEDLINE]
10.

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
[PubMed - indexed for MEDLINE]
11.

Cardiomyopathic and channelopathic causes of sudden unexplained death in infants and children.

Tester DJ, Ackerman MJ.

Annu Rev Med. 2009;60:69-84. doi: 10.1146/annurev.med.60.052907.103838. Review.

PMID:
18928334
[PubMed - indexed for MEDLINE]
12.

L-type Ca2+ channel function during Timothy syndrome.

Dixon RE, Cheng EP, Mercado JL, Santana LF.

Trends Cardiovasc Med. 2012 Apr;22(3):72-6. doi: 10.1016/j.tcm.2012.06.015. Review.

PMID:
22999068
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Identifying potential functional impact of mutations and polymorphisms: linking heart failure, increased risk of arrhythmias and sudden cardiac death.

Jagu B, Charpentier F, Toumaniantz G.

Front Physiol. 2013 Sep 20;4:254. doi: 10.3389/fphys.2013.00254. Review.

PMID:
24065925
[PubMed]
Free PMC Article
14.

Resurgence of sodium channel research.

Goldin AL.

Annu Rev Physiol. 2001;63:871-94. Review.

PMID:
11181979
[PubMed - indexed for MEDLINE]

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