Laksman ZW - Search Results

1

Steinberg C, Dognin N, Sodhi A, Champagne C, Staples JA, Champagne J, Laksman ZW, Sarrazin JF, Bennett MT, Plourde B, Deyell MW, Andrade JG, Roy K, Yeung-Lai-Wah JA, Hawkins NM, Mondésert B, Blier L, Nault I, O'Hara G, Krahn AD, Philippon F, Chakrabarti S. Steinberg C, et al. Among authors: laksman zw. Circulation. 2022 Mar 8;145(10):742-753. doi: 10.1161/CIRCULATIONAHA.121.056471. Epub 2021 Dec 16. Circulation. 2022. PMID: 34913361

2

Targeted activation of human ether-à-go-go-related gene channels rescues electrical instability induced by the R56Q+/- long QT syndrome variant.

Venkateshappa R, Hunter DV, Muralidharan P, Nagalingam RS, Huen G, Faizi S, Luthra S, Lin E, Cheng YM, Hughes J, Khelifi R, Dhunna DP, Johal R, Sergeev V, Shafaattalab S, Julian LM, Poburko DT, Laksman Z, Tibbits GF, Claydon TW. Venkateshappa R, et al. Cardiovasc Res. 2023 Nov 25;119(15):2522-2535. doi: 10.1093/cvr/cvad155. Cardiovasc Res. 2023. PMID: 37739930

3

Mutation location effect on severity of phenotype during exercise testing in type 1 long-QT syndrome: impact of transmembrane and C-loop location.

Laksman ZW, Hamilton RM, Chockalingam P, Ballantyne E, Stephenson EA, Gross GJ, Gula LJ, Klein GJ, Wilde AA, Krahn AD. Laksman ZW, et al. J Cardiovasc Electrophysiol. 2013 Sep;24(9):1015-20. doi: 10.1111/jce.12172. Epub 2013 May 20. J Cardiovasc Electrophysiol. 2013. PMID: 23691991

4

Exercise testing in asymptomatic gene carriers exposes a latent electrical substrate of arrhythmogenic right ventricular cardiomyopathy.

Perrin MJ, Angaran P, Laksman Z, Zhang H, Porepa LF, Rutberg J, James C, Krahn AD, Judge DP, Calkins H, Gollob MH. Perrin MJ, et al. J Am Coll Cardiol. 2013 Nov 5;62(19):1772-9. doi: 10.1016/j.jacc.2013.04.084. Epub 2013 Jun 27. J Am Coll Cardiol. 2013. PMID: 23810883 Free article.

5

Evolution of a genetic diagnosis.

Laksman Z, Dulay D, Gollob MH, Skanes AC, Krahn AD. Laksman Z, et al. Clin Genet. 2014 Dec;86(6):580-4. doi: 10.1111/cge.12320. Epub 2013 Dec 20. Clin Genet. 2014. PMID: 24237251

6

Arrhythmogenic right ventricular cardiomyopathy with recessive inheritance related to a new homozygous desmocollin-2 mutation.

Al-Sabeq B, Krahn AD, Conacher S, Klein GJ, Laksman Z. Al-Sabeq B, et al. Can J Cardiol. 2014 Jun;30(6):696.e1-3. doi: 10.1016/j.cjca.2014.01.014. Epub 2014 Jan 23. Can J Cardiol. 2014. PMID: 24793512

7

Early repolarization is associated with symptoms in patients with type 1 and type 2 long QT syndrome.

Laksman ZW, Gula LJ, Saklani P, Cassagneau R, Steinberg C, Conacher S, Yee R, Skanes A, Leong-Sit P, Manlucu J, Klein GJ, Krahn AD. Laksman ZW, et al. Heart Rhythm. 2014 Sep;11(9):1632-8. doi: 10.1016/j.hrthm.2014.05.027. Epub 2014 May 24. Heart Rhythm. 2014. PMID: 24861447

8

Greater mortality risk among patients with delayed follow-up after implantable cardioverter defibrillator procedures.

Laksman ZW, Krahn AD, Dorian P, Simpson CS, Crystal E, Healey JS, Khaykin Y, Wang X, Lee DS. Laksman ZW, et al. Can J Cardiol. 2014 Jun;30(6):598-605. doi: 10.1016/j.cjca.2014.03.028. Epub 2014 Mar 27. Can J Cardiol. 2014. PMID: 24882529

9

Reduced Uptake of Family Screening in Genotype-Negative Versus Genotype-Positive Long QT Syndrome.

Hanninen M, Klein GJ, Laksman Z, Conacher SS, Skanes AC, Yee R, Gula LJ, Leong-Sit P, Manlucu J, Krahn AD. Hanninen M, et al. J Genet Couns. 2015 Aug;24(4):558-64. doi: 10.1007/s10897-014-9776-6. Epub 2014 Oct 3. J Genet Couns. 2015. PMID: 25273952

10

A detailed description and assessment of outcomes of patients with hospital recorded QTc prolongation.

Laksman Z, Momciu B, Seong YW, Burrows P, Conacher S, Manlucu J, Leong-Sit P, Gula LJ, Skanes AC, Yee R, Klein GJ, Krahn AD. Laksman Z, et al. Am J Cardiol. 2015 Apr 1;115(7):907-11. doi: 10.1016/j.amjcard.2015.01.016. Epub 2015 Jan 15. Am J Cardiol. 2015. PMID: 25665761

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