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Results: 1 to 20 of 110

1.

The role of ion channelopathies in sudden cardiac death: implications for clinical practice.

Martin CA, Huang CL, Matthews GD.

Ann Med. 2013 Jun;45(4):364-74. doi: 10.3109/07853890.2013.783994. Epub 2013 May 8. Review.

PMID:
23651009
[PubMed - indexed for MEDLINE]
2.

Recent developments in the management of patients at risk for sudden cardiac death.

Martin CA, Huang CL, Matthews GD.

Postgrad Med. 2011 Mar;123(2):84-94. doi: 10.3810/pgm.2011.03.2266. Review.

PMID:
21474896
[PubMed - indexed for MEDLINE]
3.

[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]
4.

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]
5.

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]
6.

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]
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.

Genetics and sudden death.

Lombardi R.

Curr Opin Cardiol. 2013 May;28(3):272-81. doi: 10.1097/HCO.0b013e32835fb7f3. Review.

PMID:
23549233
[PubMed - indexed for MEDLINE]
9.

[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]
10.

Sudden cardiac death and inherited channelopathy: the basic electrophysiology of the myocyte and myocardium in ion channel disease.

Martin CA, Matthews GD, Huang CL.

Heart. 2012 Apr;98(7):536-43. doi: 10.1136/heartjnl-2011-300953. Review.

PMID:
22422742
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

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
12.

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]
13.

Depolarization/repolarization, electrocardiographic abnormalities, and arrhythmias in cardiac channelopathies.

Marcus FI.

J Electrocardiol. 2005 Oct;38(4 Suppl):60-3. Review.

PMID:
16226076
[PubMed - indexed for MEDLINE]
14.

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]
15.

Genetics and cardiac channelopathies.

Campuzano O, Beltrán-Alvarez P, Iglesias A, Scornik F, Pérez G, Brugada R.

Genet Med. 2010 May;12(5):260-7. doi: 10.1097/GIM.0b013e3181d81636. Review.

PMID:
20386317
[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.

[Molecular genetic aspects of arrhythmias].

Novotný T.

Vnitr Lek. 2003 Sep;49(9):768-72. Czech.

PMID:
14584430
[PubMed - indexed for MEDLINE]
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
[PubMed - indexed for MEDLINE]
19.

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
20.

Long and short QT syndrome.

Borchert B, Lawrenz T, Stellbrink C.

Herzschrittmacherther Elektrophysiol. 2006 Dec;17(4):205-10. Review.

PMID:
17211751
[PubMed - indexed for MEDLINE]

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