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Items: 1 to 20 of 133

1.

Genetic Testing in the Evaluation of Unexplained Cardiac Arrest: From the CASPER (Cardiac Arrest Survivors With Preserved Ejection Fraction Registry).

Mellor G, Laksman ZWM, Tadros R, Roberts JD, Gerull B, Simpson CS, Klein GJ, Champagne J, Talajic M, Gardner M, Steinberg C, Arbour L, Birnie DH, Angaran P, Leather R, Sanatani S, Chauhan VS, Seifer C, Healey JS, Krahn AD.

Circ Cardiovasc Genet. 2017 Jun;10(3). pii: e001686. doi: 10.1161/CIRCGENETICS.116.001686.

PMID:
28600387
2.

Beyond the Electrocardiogram: Mutations in Cardiac Ion Channel Genes Underlie Nonarrhythmic Phenotypes.

Roston TM, Cunningham T, Lehman A, Laksman ZW, Krahn AD, Sanatani S.

Clin Med Insights Cardiol. 2017 Mar 16;11:1179546817698134. doi: 10.1177/1179546817698134. eCollection 2017. Review.

3.

The role of the autonomic nervous system in arrhythmias and sudden cardiac death.

Franciosi S, Perry FKG, Roston TM, Armstrong KR, Claydon VE, Sanatani S.

Auton Neurosci. 2017 Jul;205:1-11. doi: 10.1016/j.autneu.2017.03.005. Epub 2017 Mar 31. Review.

PMID:
28392310
4.

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.

Can J Cardiol. 2017 Jun;33(6):814-821. doi: 10.1016/j.cjca.2016.12.009. Epub 2016 Dec 20.

PMID:
28347582
5.

Pharmacogenomic screening for anthracycline-induced cardiotoxicity in childhood cancer.

Aminkeng F, Ross CJD, Rassekh SR, Rieder MJ, Bhavsar AP, Sanatani S, Bernstein D, Hayden MR, Amstutz U, Carleton BC.

Br J Clin Pharmacol. 2017 May;83(5):1143-1145. doi: 10.1111/bcp.13218. Epub 2017 Mar 19. No abstract available.

PMID:
28317142
6.

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.

J Med Genet. 2017 Jun;54(6):390-398. doi: 10.1136/jmedgenet-2016-104153. Epub 2017 Mar 6.

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.

Circ Cardiovasc Genet. 2017 Jan;10(1). pii: e001537. doi: 10.1161/CIRCGENETICS.116.001537.

PMID:
28196901
8.

The clinical and genetic spectrum of catecholaminergic polymorphic ventricular tachycardia: findings from an international multicentre registry.

Roston TM, Yuchi Z, Kannankeril PJ, Hathaway J, Vinocur JM, Etheridge SP, Potts JE, Maginot KR, Salerno JC, Cohen MI, Hamilton RM, Pflaumer A, Mohammed S, Kimlicka L, Kanter RJ, LaPage MJ, Collins KK, Gebauer RA, Temple JD, Batra AS, Erickson C, Miszczak-Knecht M, Kubuš P, Bar-Cohen Y, Kantoch M, Thomas VC, Hessling G, Anderson C, Young ML, Choi SHJ, Cabrera Ortega M, Lau YR, Johnsrude CL, Fournier A, Van Petegem F, Sanatani S.

Europace. 2017 Jan 31. doi: 10.1093/europace/euw389. [Epub ahead of print]

PMID:
28158428
9.

Genetic Insurance Discrimination in Sudden Arrhythmia Death Syndromes: Empirical Evidence From a Cross-Sectional Survey in North America.

Mohammed S, Lim Z, Dean PH, Potts JE, Tang JN, Etheridge SP, Lara A, Husband P, Sherwin ED, Ackerman MJ, Sanatani S.

Circ Cardiovasc Genet. 2017 Jan;10(1). pii: e001442. doi: 10.1161/CIRCGENETICS.116.001442.

PMID:
28119333
10.

Exercise and the multidisciplinary holistic approach to adolescent dysautonomia.

Armstrong KR, De Souza AM, Sneddon PL, Potts JE, Claydon VE, Sanatani S.

Acta Paediatr. 2017 Apr;106(4):612-618. doi: 10.1111/apa.13750. Epub 2017 Feb 19.

PMID:
28112424
11.

Morbidities in the ultra-athlete and marathoner.

Cunningham TC, Maghrabi K, Sanatani S.

Cardiol Young. 2017 Jan;27(S1):S94-S100. doi: 10.1017/S1047951116002304. Review.

PMID:
28084966
12.

Advances in the diagnosis and treatment of catecholaminergic polymorphic ventricular tachycardia.

Roston TM, Cunningham TC, Sanatani S.

Cardiol Young. 2017 Jan;27(S1):S49-S56. doi: 10.1017/S1047951116002237. Review.

PMID:
28084961
13.

Catecholaminergic polymorphic ventricular tachycardia: a model for genotype-specific therapy.

Roston TM, Van Petegem F, Sanatani S.

Curr Opin Cardiol. 2017 Jan;32(1):78-85.

PMID:
27861184
14.

Management of Gene-Positive Catecholaminergic Polymorphic Ventricular Tachycardia: Are the Long Term Outcomes on Therapy Really So Poor?

Roston TM, Sanatani S.

Circ J. 2016 Nov 25;80(12):2565. Epub 2016 Nov 11. No abstract available.

15.

Canadian Cardiovascular Society and Canadian Pediatric Cardiology Association Position Statement on the Approach to Syncope in the Pediatric Patient.

Sanatani S, Chau V, Fournier A, Dixon A, Blondin R, Sheldon RS.

Can J Cardiol. 2017 Feb;33(2):189-198. doi: 10.1016/j.cjca.2016.09.006. Epub 2016 Oct 3.

PMID:
27838109
16.

Suppression-of-function mutations in the cardiac ryanodine receptor: Emerging evidence for a novel arrhythmia syndrome?

Roston TM, Sanatani S, Chen SR.

Heart Rhythm. 2017 Jan;14(1):108-109. doi: 10.1016/j.hrthm.2016.11.004. Epub 2016 Nov 3. No abstract available.

PMID:
27818320
17.

A novel RYR2 loss-of-function mutation (I4855M) is associated with left ventricular non-compaction and atypical catecholaminergic polymorphic ventricular tachycardia.

Roston TM, Guo W, Krahn AD, Wang R, Van Petegem F, Sanatani S, Chen SR, Lehman A.

J Electrocardiol. 2017 Mar - Apr;50(2):227-233. doi: 10.1016/j.jelectrocard.2016.09.006. Epub 2016 Sep 8.

PMID:
27646203
18.

Cardiac Abnormalities in First-Degree Relatives of Unexplained Cardiac Arrest Victims: A Report From the Cardiac Arrest Survivors With Preserved Ejection Fraction Registry.

Steinberg C, Padfield GJ, Champagne J, Sanatani S, Angaran P, Andrade JG, Roberts JD, Healey JS, Chauhan VS, Birnie DH, Janzen M, Gerull B, Klein GJ, Leather R, Simpson CS, Seifer C, Talajic M, Gardner M, Krahn AD.

Circ Arrhythm Electrophysiol. 2016 Sep;9(9). pii: e004274. doi: 10.1161/CIRCEP.115.004274.

PMID:
27635072
19.

A Clinical Risk Score to Improve the Diagnosis of Tachycardia-Induced Cardiomyopathy in Childhood.

Moore JP, Wang S, Albers EL, Salerno JC, Stephenson EA, Shah MJ, Pflaumer A, Czosek RJ, Garnreiter JM, Collins K, Papez AL, Sanatani S, Cain NB, Kannankeril PJ, Perry JC, Mandapati R, Silva JN, Balaji S, Shannon KM.

Am J Cardiol. 2016 Oct 1;118(7):1074-80. doi: 10.1016/j.amjcard.2016.07.008. Epub 2016 Jul 18.

PMID:
27515893
20.

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.

Can J Cardiol. 2016 Dec;32(12):1396-1401. doi: 10.1016/j.cjca.2016.04.004. Epub 2016 Apr 21.

PMID:
27474350

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