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Results: 1 to 20 of 68

Related Articles by Review for PubMed (Select 21215473)

1.

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.

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
3.

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.

4.

Sudden Infant Death Syndrome: review of implicated genetic factors.

Weese-Mayer DE, Ackerman MJ, Marazita ML, Berry-Kravis EM.

Am J Med Genet A. 2007 Apr 15;143A(8):771-88. Review.

PMID:
17340630
5.

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

Tester DJ, Ackerman MJ.

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

6.

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.

7.

[Postmortem genetic testing in sudden cardiac death due to ion channelopathies].

Guan DW, Zhao R.

Fa Yi Xue Za Zhi. 2010 Apr;26(2):120-7. Review. Chinese.

PMID:
20653139
8.

[Ion channel disorders and arrhythmia--special reference to long QT syndrome and Brugada syndrome].

Shimizu W.

Nihon Naika Gakkai Zasshi. 2006 Nov 10;95(11):2321-9. Review. Japanese. No abstract available.

PMID:
17168410
9.

Role of pharmacotherapy in cardiac ion channelopathies.

El-Sherif N, Pedalino R, Himel H 4th.

Curr Vasc Pharmacol. 2009 Jul;7(3):358-66. Review.

PMID:
19601860
10.

Sudden cardiac death with normal heart: molecular autopsy.

Basso C, Carturan E, Pilichou K, Rizzo S, Corrado D, Thiene G.

Cardiovasc Pathol. 2010 Nov-Dec;19(6):321-5. doi: 10.1016/j.carpath.2010.02.003. Epub 2010 Apr 9. Review.

PMID:
20381381
11.
12.

[Molecular tests for (early) recognition of heart disease - genetic studies in lethal inherited cardiac arrhythmias].

Keller DI.

Ther Umsch. 2010 Jul;67(7):341-8. doi: 10.1024/0040-5930/a000062. Review. German.

PMID:
20577962
13.

The inherited long QT syndrome: from ion channel to bedside.

Vincent GM, Timothy K, Fox J, Zhang L.

Cardiol Rev. 1999 Jan-Feb;7(1):44-55. Review.

PMID:
10348966
15.

The genetic and clinical features of cardiac channelopathies.

Roberts JD, Gollob MH.

Future Cardiol. 2010 Jul;6(4):491-506. doi: 10.2217/fca.10.27. Review.

PMID:
20608822
16.

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.

17.

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
18.

Phenotypic manifestations of mutations in genes encoding subunits of cardiac potassium channels.

Shimizu W, Horie M.

Circ Res. 2011 Jun 24;109(1):97-109. doi: 10.1161/CIRCRESAHA.110.224600. Review.

19.

Arrhythmogenic hereditary syndromes: Brugada Syndrome, long QT syndrome, short QT syndrome and CPVT.

Schimpf R, Veltmann C, Wolpert C, Borggrefe M.

Minerva Cardioangiol. 2010 Dec;58(6):623-36. Review.

PMID:
21135804
20.

[Cardiac ion channel disorders--diagnosis and treatment].

Haugaa KH, Berge KE, Früh A, Anfinsen OG, Arnestad M, Hallerud M, Gjesdal K, Leren TP, Amlie JP.

Tidsskr Nor Laegeforen. 2005 Oct 20;125(20):2778-81. Review. Norwegian.

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