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Model-based navigation of left and right ventricular leads to optimal targets for cardiac resynchronization therapy: a single-center feasibility study.
Laksman Z, Yee R, Stirrat J, Gula LJ, Skanes AC, Leong-Sit P, Manlucu J, McCarty D, Turkistani Y, Scholl D, Rajchl M, Goela A, Islam A, Thompson RT, Drangova M, White JA. Laksman Z, et al. Circ Arrhythm Electrophysiol. 2014 Dec;7(6):1040-7. doi: 10.1161/CIRCEP.114.001729. Epub 2014 Sep 14. Circ Arrhythm Electrophysiol. 2014. PMID: 25221334
Generation of an induced pluripotent stem cell line from a patient with conduction disease and recurrent ventricular fibrillation with a sodium voltage-gated channel alpha subunit 5 (SCN5A) gene c.392 + 3A > G splice-site variant.
Li S, Fraser S, Ranpura G, Lim S, Singer ES, Parker JDK, Crowe J, Bagnall RD, Laksman Z, Semsarian C. Li S, et al. Among authors: laksman z. Stem Cell Res. 2023 Sep;71:103153. doi: 10.1016/j.scr.2023.103153. Epub 2023 Jun 23. Stem Cell Res. 2023. PMID: 37385135 Free article.
Provocation testing in congenital long QT syndrome: A practical guide.
Abrahams T, Davies B, Laksman Z, Sy RW, Postema PG, Wilde AAM, Krahn AD, Han HC. Abrahams T, et al. Among authors: laksman z. Heart Rhythm. 2023 Nov;20(11):1570-1582. doi: 10.1016/j.hrthm.2023.07.059. Epub 2023 Jul 20. Heart Rhythm. 2023. PMID: 37481219 Review.
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. Among authors: laksman z. Cardiovasc Res. 2023 Nov 25;119(15):2522-2535. doi: 10.1093/cvr/cvad155. Cardiovasc Res. 2023. PMID: 37739930
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
123 results