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Items: 1 to 20 of 110

1.

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
2.

Systematic assessment of patients with unexplained cardiac arrest: Cardiac Arrest Survivors With Preserved Ejection Fraction Registry (CASPER).

Krahn AD, Healey JS, Chauhan V, Birnie DH, Simpson CS, Champagne J, Gardner M, Sanatani S, Exner DV, Klein GJ, Yee R, Skanes AC, Gula LJ, Gollob MH.

Circulation. 2009 Jul 28;120(4):278-85. doi: 10.1161/CIRCULATIONAHA.109.853143. Epub 2009 Jul 13. Erratum in: Circulation. 2010 Jun 29;121(25):e460.

3.

Evolution of clinical diagnosis in patients presenting with unexplained cardiac arrest or syncope due to polymorphic ventricular tachycardia.

Vittoria Matassini M, Krahn AD, Gardner M, Champagne J, Sanatani S, Birnie DH, Gollob MH, Chauhan V, Simpson CS, Hamilton RM, Talajic M, Ahmad K, Gerull B, Chakrabarti S, Healey JS.

Heart Rhythm. 2014 Feb;11(2):274-81. doi: 10.1016/j.hrthm.2013.11.008. Epub 2013 Nov 14.

PMID:
24239842
4.

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
5.

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.

6.

Epinephrine infusion in the evaluation of unexplained cardiac arrest and familial sudden death: from the cardiac arrest survivors with preserved Ejection Fraction Registry.

Krahn AD, Healey JS, Chauhan VS, Birnie DH, Champagne J, Sanatani S, Ahmad K, Ballantyne E, Gerull B, Yee R, Skanes AC, Gula LJ, Leong-Sit P, Klein GJ, Gollob MH, Simpson CS, Talajic M, Gardner M.

Circ Arrhythm Electrophysiol. 2012 Oct;5(5):933-40. doi: 10.1161/CIRCEP.112.973230. Epub 2012 Sep 3.

7.

Identification of a common genetic substrate underlying postpartum cardiac events in congenital long QT syndrome.

Khositseth A, Tester DJ, Will ML, Bell CM, Ackerman MJ.

Heart Rhythm. 2004 May;1(1):60-4.

PMID:
15851119
8.
9.

Deadly proposal: a case of catecholaminergic polymorphic ventricular tachycardia.

Heiner JD, Bullard-Berent JH, Inbar S.

Pediatr Emerg Care. 2011 Nov;27(11):1065-8. doi: 10.1097/PEC.0b013e3182360606.

PMID:
22068070
10.

Genetic testing in the management of inherited arrhythmia syndromes.

Tzou WS, Gerstenfeld EP.

Curr Cardiol Rep. 2009 Sep;11(5):343-51. Review.

PMID:
19709494
11.

Diagnosis of unexplained cardiac arrest: role of adrenaline and procainamide infusion.

Krahn AD, Gollob M, Yee R, Gula LJ, Skanes AC, Walker BD, Klein GJ.

Circulation. 2005 Oct 11;112(15):2228-34. Epub 2005 Oct 3.

12.

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.

13.

Sentinel symptoms in patients with unexplained cardiac arrest: from the cardiac arrest survivors with preserved ejection fraction registry (CASPER).

Krahn AD, Healey JS, Simpson CS, Chauhan VS, Birnie DH, Champagne J, Gardner M, Sanatani S, Chakrabarti S, Yee R, Skanes AC, Leong-Sit P, Ahmad K, Gollob MH, Klein GJ, Gula LJ, Sheldon RS.

J Cardiovasc Electrophysiol. 2012 Jan;23(1):60-6. doi: 10.1111/j.1540-8167.2011.02185.x. Epub 2011 Sep 28.

PMID:
21955300
14.

The molecular autopsy: an indispensable step following sudden cardiac death in the young?

Boczek NJ, Tester DJ, Ackerman MJ.

Herzschrittmacherther Elektrophysiol. 2012 Sep;23(3):167-73. doi: 10.1007/s00399-012-0222-x. Epub 2012 Sep 20.

15.

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.

Inherited heart rhythm disease: negotiating the minefield for the practicing cardiologist.

Krahn AD, Sanatani S, Gardner MJ, Arbour L.

Can J Cardiol. 2013 Jan;29(1):122-5. doi: 10.1016/j.cjca.2012.11.009. Review.

PMID:
23261322
18.

The genetics of cardiac disease associated with sudden cardiac death: a paper from the 2011 William Beaumont Hospital Symposium on molecular pathology.

Perrin MJ, Gollob MH.

J Mol Diagn. 2012 Sep;14(5):424-36. doi: 10.1016/j.jmoldx.2012.04.002. Epub 2012 Jun 27. Review.

PMID:
22749884
19.
20.

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
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