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Items: 1 to 20 of 124

1.

Cardiac ion channelopathies and the sudden infant death syndrome.

Wilders R.

ISRN Cardiol. 2012;2012:846171. doi: 10.5402/2012/846171. Epub 2012 Dec 5.

2.

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.

3.

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
4.

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.

5.

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
6.

The sudden infant death syndrome gene: does it exist?

Opdal SH, Rognum TO.

Pediatrics. 2004 Oct;114(4):e506-12.

PMID:
15466077
7.
8.

Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome.

Ackerman MJ, Siu BL, Sturner WQ, Tester DJ, Valdivia CR, Makielski JC, Towbin JA.

JAMA. 2001 Nov 14;286(18):2264-9.

PMID:
11710892
9.

[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
10.

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.

11.

Cardiac Channelopathies and Sudden Death: Recent Clinical and Genetic Advances.

Fernández-Falgueras A, Sarquella-Brugada G, Brugada J, Brugada R, Campuzano O.

Biology (Basel). 2017 Jan 29;6(1). pii: E7. doi: 10.3390/biology6010007. Review.

12.

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
13.

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
14.

Postmortem review and genetic analysis in sudden infant death syndrome: an 11-year review.

Evans A, Bagnall RD, Duflou J, Semsarian C.

Hum Pathol. 2013 Sep;44(9):1730-6. doi: 10.1016/j.humpath.2013.01.024. Epub 2013 Apr 25.

PMID:
23623143
15.

Role of pharmacotherapy in cardiac ion channelopathies.

El-Sherif N, Boutjdir M.

Pharmacol Ther. 2015 Nov;155:132-42. doi: 10.1016/j.pharmthera.2015.09.002. Epub 2015 Sep 12. Review.

PMID:
26376080
16.

Sudden infant death syndrome caused by cardiac arrhythmias: only a matter of genes encoding ion channels?

Sarquella-Brugada G, Campuzano O, Cesar S, Iglesias A, Fernandez A, Brugada J, Brugada R.

Int J Legal Med. 2016 Mar;130(2):415-20. doi: 10.1007/s00414-016-1330-7. Epub 2016 Feb 12. Review.

PMID:
26872470
17.

The role of molecular autopsy in unexplained sudden cardiac death.

Tester DJ, Ackerman MJ.

Curr Opin Cardiol. 2006 May;21(3):166-72. Review.

PMID:
16601452
18.

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
19.

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
20.

Sudden infant death syndrome and long QT syndrome: an epidemiological and genetic study.

Wedekind H, Bajanowski T, Friederich P, Breithardt G, Wülfing T, Siebrands C, Engeland B, Mönnig G, Haverkamp W, Brinkmann B, Schulze-Bahr E.

Int J Legal Med. 2006 May;120(3):129-37. Epub 2005 Jul 13.

PMID:
16012827

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