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Items: 1 to 20 of 145

1.

Genetics of cardiac electrical disease.

Perrin MJ, Gollob MH.

Can J Cardiol. 2013 Jan;29(1):89-99. doi: 10.1016/j.cjca.2012.07.847. Epub 2012 Oct 11. Review.

PMID:
23062665
2.

Sudden cardiac death and inherited arrhythmia syndromes.

Sarkozy A, Brugada P.

J Cardiovasc Electrophysiol. 2005 Sep;16 Suppl 1:S8-20. Review.

PMID:
16138889
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
4.

Inherited arrhythmia syndromes.

Wilde AA, Tan HL.

Circ J. 2007;71 Suppl A:A12-9. Review.

5.

Genetic testing and genetic counseling in patients with sudden death risk due to heritable arrhythmias.

Spoonamore KG, Ware SM.

Heart Rhythm. 2016 Mar;13(3):789-97. doi: 10.1016/j.hrthm.2015.11.013. Epub 2015 Nov 12. Review.

PMID:
26582592
6.

[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
7.

[Sudden cardiac death and inherited repolarization disorders].

Gościńska K, Sredniawa B, Pasyk S.

Przegl Lek. 2002;59(7):523-6. Review. Polish.

PMID:
12516242
8.

Electrocardiographic transmural dispersion of repolarization in patients with inherited short QT syndrome.

Anttonen O, Väänänen H, Junttila J, Huikuri HV, Viitasalo M.

Ann Noninvasive Electrocardiol. 2008 Jul;13(3):295-300. doi: 10.1111/j.1542-474X.2008.00234.x.

PMID:
18713331
9.

Genetic arrhythmias.

Priori SG, Cerrone M.

Ital Heart J. 2005 Mar;6(3):241-8. Review.

PMID:
15875515
10.

Genetic basis of malignant channelopathies and ventricular fibrillation in the structurally normal heart.

Hofman N, van Lochem LT, Wilde AA.

Future Cardiol. 2010 May;6(3):395-408. doi: 10.2217/fca.10.11. Review.

PMID:
20462344
11.

Active cascade screening in primary inherited arrhythmia syndromes: does it lead to prophylactic treatment?

Hofman N, Tan HL, Alders M, van Langen IM, Wilde AA.

J Am Coll Cardiol. 2010 Jun 8;55(23):2570-6. doi: 10.1016/j.jacc.2009.12.063.

12.

Clinical and molecular genetics of the short QT syndrome.

Schimpf R, Borggrefe M, Wolpert C.

Curr Opin Cardiol. 2008 May;23(3):192-8. doi: 10.1097/HCO.0b013e3282fbf756. Review.

PMID:
18382206
13.

Cardiac conduction disorders in children.

Steffensen TS, Barness EG.

Front Biosci (Elite Ed). 2009 Jun 1;1:519-27. Review.

PMID:
19482666
14.

Congenital short QT syndrome. A review.

Ginghină C, Ciudin R, Lăpuşanu O, Kulcsar I, Selaru A, Gherasim D.

Rom J Intern Med. 2005;43(3-4):165-72. Review.

PMID:
16812977
15.

Assessment of genetic causes of cardiac arrest.

Bennett MT, Sanatani S, Chakrabarti S, Deyell MW, Krahn AD.

Can J Cardiol. 2013 Jan;29(1):100-10. doi: 10.1016/j.cjca.2012.07.002. Epub 2012 Nov 27. Review.

PMID:
23200097
16.

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
17.

Transmural dispersion of repolarization and arrhythmogenicity: the Brugada syndrome versus the long QT syndrome.

Antzelevitch C, Yan GX, Shimizu W.

J Electrocardiol. 1999;32 Suppl:158-65. Review.

PMID:
10688320
19.

Disorders of cardiac repolarization: long QT and short QT syndromes.

Horie M, Itoh H.

Circ J. 2007;71 Suppl A:A50-3. Review.

20.

Sudden unexplained death: heritability and diagnostic yield of cardiological and genetic examination in surviving relatives.

Tan HL, Hofman N, van Langen IM, van der Wal AC, Wilde AA.

Circulation. 2005 Jul 12;112(2):207-13. Epub 2005 Jul 5.

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