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Results: 1 to 20 of 122

1.

[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
[PubMed - indexed for MEDLINE]
2.

[Sudden cardiac death in athletes with an apparently normal heart: the channelopathies].

Giustetto C, Gaita F.

G Ital Cardiol (Rome). 2008 Oct;9(10 Suppl 1):78S-82S. Italian.

PMID:
19195312
[PubMed - indexed for MEDLINE]
3.

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.

PMID:
22529064
[PubMed - indexed for MEDLINE]
Free Article
4.

Screening for, and management of, possible arrhythmogenic syndromes (channelopathies/ion channel diseases).

Svendsen JH, Geelen P; EHRA Scientific Initiative Commitee.

Europace. 2010 May;12(5):741-2. doi: 10.1093/europace/euq126.

PMID:
20421225
[PubMed - indexed for MEDLINE]
Free Article
5.

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
[PubMed - indexed for MEDLINE]
6.

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
[PubMed - indexed for MEDLINE]
7.

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
[PubMed - indexed for MEDLINE]
8.

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.

PMID:
23074337
[PubMed - indexed for MEDLINE]
Free Article
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
[PubMed - indexed for MEDLINE]
10.

[Hereditary risk of sudden cardiac death--genetic investigation of the family].

Lundin C, Platonov P, Kristoffersson U.

Lakartidningen. 2009 Apr 7-21;106(15-16):1089-93. Review. Swedish. No abstract available.

PMID:
19492675
[PubMed - indexed for MEDLINE]
11.

Genetic testing for cardiac channelopathies: ten questions regarding clinical considerations for heart rhythm allied professionals.

Tester DJ, Ackerman MJ.

Heart Rhythm. 2005 Jun;2(6):675-7. Review. No abstract available.

PMID:
15922282
[PubMed - indexed for MEDLINE]
12.

Polymorphic ventricular tachycardia--part II: the channelopathies.

Choudhuri I, Pinninti M, Marwali MR, Sra J, Akhtar M.

Curr Probl Cardiol. 2013 Dec;38(12):503-48. doi: 10.1016/j.cpcardiol.2013.07.004. Review.

PMID:
24262155
[PubMed - indexed for MEDLINE]
14.

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.

PMID:
17586620
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

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.

PMID:
19808439
[PubMed - indexed for MEDLINE]
Free Article
16.

How to perform and interpret provocative testing for the diagnosis of Brugada syndrome, long-QT syndrome, and catecholaminergic polymorphic ventricular tachycardia.

Obeyesekere MN, Klein GJ, Modi S, Leong-Sit P, Gula LJ, Yee R, Skanes AC, Krahn AD.

Circ Arrhythm Electrophysiol. 2011 Dec;4(6):958-64. doi: 10.1161/CIRCEP.111.965947. Review. No abstract available.

PMID:
22203660
[PubMed - indexed for MEDLINE]
Free Article
17.

Short and long QT syndromes: does QT length really matter?

Couderc JP, Lopes CM.

J Electrocardiol. 2010 Sep-Oct;43(5):396-9. doi: 10.1016/j.jelectrocard.2010.07.009. Review.

PMID:
20728018
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Genetics and arrhythmias: diagnostic and prognostic applications.

Monteforte N, Napolitano C, Priori SG.

Rev Esp Cardiol (Engl Ed). 2012 Mar;65(3):278-86. doi: 10.1016/j.recesp.2011.10.008. Epub 2012 Jan 14. Review. English, Spanish.

PMID:
22245453
[PubMed - indexed for MEDLINE]
19.

Primary electrical diseases diagnosis, genetic and management.

Maury P, Duparc A, Mondoly P, Rollin A, Cardin C, Delay M.

Minerva Cardioangiol. 2010 Aug;58(4):449-83. Review.

PMID:
20938412
[PubMed - indexed for MEDLINE]
20.

The differential diagnosis of primary electrical diseases from seizures in childhood.

Baruteau AE, Baruteau J, Mabo P.

Cardiol Young. 2010 Feb;20(1):111-2. doi: 10.1017/S1047951109991983. Epub 2010 Jan 13. No abstract available.

PMID:
20067655
[PubMed - indexed for MEDLINE]

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