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Items: 1 to 20 of 199

1.

Sudden cardiac death and genetic ion channelopathies: long QT, Brugada, short QT, catecholaminergic polymorphic ventricular tachycardia, and idiopathic ventricular fibrillation.

Napolitano C, Bloise R, Monteforte N, Priori SG.

Circulation. 2012 Apr 24;125(16):2027-34. doi: 10.1161/CIRCULATIONAHA.111.055947. No abstract available.

2.

Sudden death and ion channel disease: pathophysiology and implications for management.

Bastiaenen R, Behr ER.

Heart. 2011 Sep;97(17):1365-72. doi: 10.1136/hrt.2011.223883. Epub 2011 Jun 16. Review.

PMID:
21685181
3.

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
4.

A clinical approach to inherited arrhythmias.

Cerrone M, Cummings S, Alansari T, Priori SG.

Circ Cardiovasc Genet. 2012 Oct 1;5(5):581-90. doi: 10.1161/CIRCGENETICS.110.959429. Review. No abstract available.

5.

[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
6.

Sudden cardiac death: what is inside our genes?

Sarkozy A, Brugada P.

Can J Cardiol. 2005 Oct;21(12):1099-110. Review.

PMID:
16234896
7.
9.

[Cardiac ion channelopathies: A potential link between cardiomyopathies and cardiac arrhythmias].

Schimpf R, Rudic B, Tülümen E, Papavassiliu T, Dösch C, Borggrefe M.

Dtsch Med Wochenschr. 2013 Mar;138(12):591-7. doi: 10.1055/s-0032-1332973. Epub 2013 Mar 12. Review. German. No abstract available.

PMID:
23483420
10.

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
11.

Management of ventricular arrhythmias in suspected channelopathies.

Obeyesekere MN, Antzelevitch C, Krahn AD.

Circ Arrhythm Electrophysiol. 2015 Feb;8(1):221-31. doi: 10.1161/CIRCEP.114.002321. Review. No abstract available.

12.

Yield of genetic screening in inherited cardiac channelopathies: how to prioritize access to genetic testing.

Bai R, Napolitano C, Bloise R, Monteforte N, Priori SG.

Circ Arrhythm Electrophysiol. 2009 Feb;2(1):6-15. doi: 10.1161/CIRCEP.108.782888. Epub 2009 Feb 10.

13.

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
14.

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
15.

Ventricular arrhythmias and sudden cardiac death.

John RM, Tedrow UB, Koplan BA, Albert CM, Epstein LM, Sweeney MO, Miller AL, Michaud GF, Stevenson WG.

Lancet. 2012 Oct 27;380(9852):1520-9. doi: 10.1016/S0140-6736(12)61413-5. Review.

PMID:
23101719
16.
17.

Sudden cardiac death: better understanding of risks, mechanisms, and treatment.

Lopshire JC, Zipes DP.

Circulation. 2006 Sep 12;114(11):1134-6. No abstract available.

18.

Role of spatial dispersion of repolarization in inherited and acquired sudden cardiac death syndromes.

Antzelevitch C.

Am J Physiol Heart Circ Physiol. 2007 Oct;293(4):H2024-38. Epub 2007 Jun 22. Review.

19.

Sudden death: managing the family, the role of genetics.

Brugada R.

Heart. 2011 Apr;97(8):676-81. doi: 10.1136/hrt.2009.185884. No abstract available.

PMID:
21421602
20.

The molecular basis of cardiac arrhythmias.

Shivkumar K, Murali NS, Krishnan SC.

J Nucl Cardiol. 2002 Mar-Apr;9(2):206-14. Review. No abstract available.

PMID:
11986566
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