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Results: 1 to 20 of 107

1.

Gene mutations in cardiac arrhythmias: a review of recent evidence in ion channelopathies.

Hsiao PY, Tien HC, Lo CP, Juang JM, Wang YH, Sung RJ.

Appl Clin Genet. 2013 Jan 18;6:1-13. doi: 10.2147/TACG.S29676. Print 2013.

PMID:
23837003
[PubMed]
Free PMC Article
2.

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
[PubMed - indexed for MEDLINE]
3.

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]
4.

Mechanisms and clinical management of inherited channelopathies: long QT syndrome, Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia, and short QT syndrome.

Kaufman ES.

Heart Rhythm. 2009 Aug;6(8 Suppl):S51-5. doi: 10.1016/j.hrthm.2009.02.009. Epub 2009 Feb 12. Review.

PMID:
19631908
[PubMed - indexed for MEDLINE]
5.

Cardiac channelopathies: genetic and molecular mechanisms.

Abriel H, Zaklyazminskaya EV.

Gene. 2013 Mar 15;517(1):1-11. doi: 10.1016/j.gene.2012.12.061. Epub 2012 Dec 22. Review.

PMID:
23266818
[PubMed - indexed for MEDLINE]
6.

Molecular mechanisms of inherited ventricular arrhythmias.

Wichter T, Schulze-Bahr E, Eckardt L, Paul M, Levkau B, Meyborg M, Schäfers M, Haverkamp W, Breithardt G.

Herz. 2002 Dec;27(8):712-39. Review.

PMID:
12574890
[PubMed - indexed for MEDLINE]
7.

Mutation detection in congenital long QT syndrome: cardiac channel gene screen using PCR, dHPLC, and direct DNA sequencing.

Tester DJ, Will ML, Ackerman MJ.

Methods Mol Med. 2006;128:181-207.

PMID:
17071997
[PubMed - indexed for MEDLINE]
8.

Ventricular tachycardia in the absence of structural heart disease.

Srivathsan K, Lester SJ, Appleton CP, Scott LR, Munger TM.

Indian Pacing Electrophysiol J. 2005 Apr 1;5(2):106-21.

PMID:
16943951
[PubMed]
Free PMC Article
9.

Genetics of congenital long QT syndrome and Brugada syndrome.

Shimizu W.

Future Cardiol. 2008 Jul;4(4):379-89. doi: 10.2217/14796678.4.4.379.

PMID:
19804318
[PubMed]
10.

[The genetic disorders responsible for sudden cardiac death].

Harada T, Nagai R.

Nihon Rinsho. 2005 Jul;63(7):1273-83. Review. Japanese.

PMID:
16001794
[PubMed - indexed for MEDLINE]
11.

Molecular genetics of arrhythmias--a new paradigm.

Schulze-Bahr E, Haverkamp W, Borggrefe M, Wedekind H, Mönnig G, Mergenthaler J, Assmann G, Funke H, Breithardt G.

Z Kardiol. 2000;89 Suppl 4:IV12-22. Review.

PMID:
10810773
[PubMed - indexed for MEDLINE]
12.

Inherited calcium channelopathies in the pathophysiology of arrhythmias.

Venetucci L, Denegri M, Napolitano C, Priori SG.

Nat Rev Cardiol. 2012 Oct;9(10):561-75. doi: 10.1038/nrcardio.2012.93. Epub 2012 Jun 26. Review.

PMID:
22733215
[PubMed - indexed for MEDLINE]
13.

Pharmacological approach to the treatment of long and short QT syndromes.

Patel C, Antzelevitch C.

Pharmacol Ther. 2008 Apr;118(1):138-51. doi: 10.1016/j.pharmthera.2008.02.001. Review.

PMID:
18378319
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Channelopathies: Brugada syndrome, long QT syndrome, short QT syndrome, and CPVT.

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

Herz. 2009 Jun;34(4):281-8. doi: 10.1007/s00059-009-3238-1. Review.

PMID:
19575158
[PubMed - indexed for MEDLINE]
15.

The LQT syndromes--current status of molecular mechanisms.

Schulze-Bahr E, Wedekind H, Haverkamp W, Borggrefe M, Assmann G, Breithardt G, Funke H.

Z Kardiol. 1999 Apr;88(4):245-54. Review.

PMID:
10408028
[PubMed - indexed for MEDLINE]
16.

Molecular biology and cellular mechanisms of Brugada and long QT syndromes in infants and young children.

Antzelevitch C.

J Electrocardiol. 2001;34 Suppl:177-81.

PMID:
11781953
[PubMed - indexed for MEDLINE]
17.

Determinants of incomplete penetrance and variable expressivity in heritable cardiac arrhythmia syndromes.

Giudicessi JR, Ackerman MJ.

Transl Res. 2013 Jan;161(1):1-14. doi: 10.1016/j.trsl.2012.08.005. Epub 2012 Sep 17. Review.

PMID:
22995932
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Spectrum and prevalence of cardiac ryanodine receptor (RyR2) mutations in a cohort of unrelated patients referred explicitly for long QT syndrome genetic testing.

Tester DJ, Kopplin LJ, Will ML, Ackerman MJ.

Heart Rhythm. 2005 Oct;2(10):1099-105.

PMID:
16188589
[PubMed - indexed for MEDLINE]
19.

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
20.

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

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