Gollob MH - Search Results

1

Detection of genomic deletions of PKP2 in arrhythmogenic right ventricular cardiomyopathy.

Roberts JD, Herkert JC, Rutberg J, Nikkel SM, Wiesfeld AC, Dooijes D, Gow RM, van Tintelen JP, Gollob MH. Roberts JD, et al. Among authors: gollob mh. Clin Genet. 2013 May;83(5):452-6. doi: 10.1111/j.1399-0004.2012.01950.x. Epub 2012 Sep 10. Clin Genet. 2013. PMID: 22889254

2

Sudden cardiac death despite an implantable cardioverter-defibrillator in a young female with catecholaminergic ventricular tachycardia.

Mohamed U, Gollob MH, Gow RM, Krahn AD. Mohamed U, et al. Among authors: gollob mh. Heart Rhythm. 2006 Dec;3(12):1486-9. doi: 10.1016/j.hrthm.2006.08.018. Epub 2006 Aug 25. Heart Rhythm. 2006. PMID: 17161793 No abstract available.

3

Molecular autopsy in the sudden cardiac death of a young woman: a first Canadian report.

Rutberg J, Green MS, Gow RM, Geraghty MT, Honeywell C, Ewen J, Birnie DH, Tang A, Lemery R, Gollob MH. Rutberg J, et al. Among authors: gollob mh. Can J Cardiol. 2007 Sep;23(11):904-6. doi: 10.1016/s0828-282x(07)70849-8. Can J Cardiol. 2007. PMID: 17876385 Free PMC article.

4

Discrepant DNA analysis in three patients with inherited arrhythmia: molecular genetic test results deserve a second glance.

Honeywell CR, Gollob MH, Rutberg J, Gow RM, Geraghty MT. Honeywell CR, et al. Among authors: gollob mh. Am J Med Genet A. 2008 Jun 1;146A(11):1466-9. doi: 10.1002/ajmg.a.32336. Am J Med Genet A. 2008. PMID: 18449933

5

Sudden death in a young man with catecholaminergic polymorphic ventricular tachycardia and paroxysmal atrial fibrillation.

Pizzale S, Gollob MH, Gow R, Birnie DH. Pizzale S, et al. Among authors: gollob mh. J Cardiovasc Electrophysiol. 2008 Dec;19(12):1319-21. doi: 10.1111/j.1540-8167.2008.01211.x. Epub 2008 Jun 12. J Cardiovasc Electrophysiol. 2008. PMID: 18554199

6

Gain-of-function mutation of Nav1.5 in atrial fibrillation enhances cellular excitability and lowers the threshold for action potential firing.

Li Q, Huang H, Liu G, Lam K, Rutberg J, Green MS, Birnie DH, Lemery R, Chahine M, Gollob MH. Li Q, et al. Among authors: gollob mh. Biochem Biophys Res Commun. 2009 Feb 27;380(1):132-7. doi: 10.1016/j.bbrc.2009.01.052. Epub 2009 Jan 22. Biochem Biophys Res Commun. 2009. PMID: 19167345

7

Inherited cardiomyopathies mimicking arrhythmogenic right ventricular cardiomyopathy.

Roberts JD, Veinot JP, Rutberg J, Gollob MH. Roberts JD, et al. Among authors: gollob mh. Cardiovasc Pathol. 2010 Sep-Oct;19(5):316-20. doi: 10.1016/j.carpath.2009.06.003. Epub 2009 Jul 24. Cardiovasc Pathol. 2010. PMID: 19632136

8

Impact of genetic discoveries on the classification of lone atrial fibrillation.

Roberts JD, Gollob MH. Roberts JD, et al. Among authors: gollob mh. J Am Coll Cardiol. 2010 Feb 23;55(8):705-12. doi: 10.1016/j.jacc.2009.12.005. J Am Coll Cardiol. 2010. PMID: 20170805 Free article. Review.

9

Evaluation of non-synonymous NPPA single nucleotide polymorphisms in atrial fibrillation.

Roberts JD, Davies RW, Lubitz SA, Thibodeau IL, Nery PB, Birnie DH, Benjamin EJ, Lemery R, Ellinor PT, Gollob MH. Roberts JD, et al. Among authors: gollob mh. Europace. 2010 Aug;12(8):1078-83. doi: 10.1093/europace/euq161. Epub 2010 Jun 12. Europace. 2010. PMID: 20543198 Free PMC article.

10

The genetic and clinical features of cardiac channelopathies.

Roberts JD, Gollob MH. Roberts JD, et al. Among authors: gollob mh. Future Cardiol. 2010 Jul;6(4):491-506. doi: 10.2217/fca.10.27. Future Cardiol. 2010. PMID: 20608822 Review.

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