Arbour LT - Search Results

1

Jackson H, Huisman LA, Sanatani S, Arbour LT. Jackson H, et al. Among authors: arbour lt. CMAJ. 2011 Aug 9;183(11):1272-5. doi: 10.1503/cmaj.100138. Epub 2011 Apr 11. CMAJ. 2011. PMID: 21482651 Free PMC article. No abstract available.

2

A KCNQ1 V205M missense mutation causes a high rate of long QT syndrome in a First Nations community of northern British Columbia: a community-based approach to understanding the impact.

Arbour L, Rezazadeh S, Eldstrom J, Weget-Simms G, Rupps R, Dyer Z, Tibbits G, Accili E, Casey B, Kmetic A, Sanatani S, Fedida D. Arbour L, et al. Genet Med. 2008 Jul;10(7):545-50. doi: 10.1097/gim.0b013e31817c6b19. Genet Med. 2008. PMID: 18580685

3

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

Krahn AD, Sanatani S, Gardner MJ, Arbour L. Krahn AD, et al. Can J Cardiol. 2013 Jan;29(1):122-5. doi: 10.1016/j.cjca.2012.11.009. Can J Cardiol. 2013. PMID: 23261322 Review.

4

LQTS in Northern BC: homozygosity for KCNQ1 V205M presents with a more severe cardiac phenotype but with minimal impact on auditory function.

Jackson HA, McIntosh S, Whittome B, Asuri S, Casey B, Kerr C, Tang A, Arbour LT. Jackson HA, et al. Among authors: arbour lt. Clin Genet. 2014 Jul;86(1):85-90. doi: 10.1111/cge.12235. Epub 2013 Jul 30. Clin Genet. 2014. PMID: 23844633

5

Patient Recall, Interpretation, and Perspective of an Inconclusive Long QT Syndrome Genetic Test Result.

Predham S, Hathaway J, Hulait G, Arbour L, Lehman A. Predham S, et al. J Genet Couns. 2017 Feb;26(1):150-158. doi: 10.1007/s10897-016-9991-4. Epub 2016 Jul 2. J Genet Couns. 2017. PMID: 27369690

6

The Canadian Arrhythmogenic Right Ventricular Cardiomyopathy Registry: Rationale, Design, and Preliminary Recruitment.

Krahn AD, Healey JS, Gerull B, Angaran P, Chakrabarti S, Sanatani S, Arbour L, Laksman ZW, Carroll SL, Seifer C, Green M, Roberts JD, Talajic M, Hamilton R, Gardner M. Krahn AD, et al. Can J Cardiol. 2016 Dec;32(12):1396-1401. doi: 10.1016/j.cjca.2016.04.004. Epub 2016 Apr 21. Can J Cardiol. 2016. PMID: 27474350

7

Novel Variant in the ANK2 Membrane-Binding Domain Is Associated With Ankyrin-B Syndrome and Structural Heart Disease in a First Nations Population With a High Rate of Long QT Syndrome.

Swayne LA, Murphy NP, Asuri S, Chen L, Xu X, McIntosh S, Wang C, Lancione PJ, Roberts JD, Kerr C, Sanatani S, Sherwin E, Kline CF, Zhang M, Mohler PJ, Arbour LT. Swayne LA, et al. Among authors: arbour lt. Circ Cardiovasc Genet. 2017 Jan;10(1):e001537. doi: 10.1161/CIRCGENETICS.116.001537. Circ Cardiovasc Genet. 2017. PMID: 28196901 Free PMC article.

8

KCNQ1 p.L353L affects splicing and modifies the phenotype in a founder population with long QT syndrome type 1.

Kapplinger JD, Erickson A, Asuri S, Tester DJ, McIntosh S, Kerr CR, Morrison J, Tang A, Sanatani S, Arbour L, Ackerman MJ. Kapplinger JD, et al. J Med Genet. 2017 Jun;54(6):390-398. doi: 10.1136/jmedgenet-2016-104153. Epub 2017 Mar 6. J Med Genet. 2017. PMID: 28264985 Free PMC article.

9

Cost Analysis of Patients Referred for Inherited Heart Rhythm Disorder Evaluation.

Janzen ML, Cheung C, Sanatani S, Cunningham T, Kerr C, Steinberg C, Sherwin E, Arbour L, Deyell MW, Andrade JG, Lehman AM, Gula LJ, Krahn AD. Janzen ML, et al. Can J Cardiol. 2017 Jun;33(6):814-821. doi: 10.1016/j.cjca.2016.12.009. Epub 2016 Dec 20. Can J Cardiol. 2017. PMID: 28347582

10

Early Repolarization Pattern Inheritance in the Cardiac Arrest Survivors With Preserved Ejection Fraction Registry (CASPER).

Malhi N, So PP, Cheung CC, Laksman ZWM, Healey JS, Chauhan VS, Green MS, Champagne J, Steinberg C, Sanatani S, Angaran P, Duff H, Roberts JD, Arbour L, Leather R, Simpson CS, Tadros R, Talajic M, Gardner M, Siefer C, Krahn AD. Malhi N, et al. JACC Clin Electrophysiol. 2018 Nov;4(11):1473-1479. doi: 10.1016/j.jacep.2018.07.001. Epub 2018 Aug 29. JACC Clin Electrophysiol. 2018. PMID: 30466855 Free article.

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