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Year Number of Results
2007 1
2012 4
2013 2
2015 2
2016 2
2019 2
2020 6
2021 4
2022 7
2023 5
2024 3

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36 results

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Page 1
The role of mutations in the SCN5A gene in cardiomyopathies.
Zaklyazminskaya E, Dzemeshkevich S. Zaklyazminskaya E, et al. Biochim Biophys Acta. 2016 Jul;1863(7 Pt B):1799-805. doi: 10.1016/j.bbamcr.2016.02.014. Epub 2016 Feb 23. Biochim Biophys Acta. 2016. PMID: 26916278 Free article. Review.
Editorial: Inherited Arrhythmias of the Cardiac Sodium Channel Nav1.5.
Amarouch MY, Zaklyazminskaya EV, Rougier JS. Amarouch MY, et al. Among authors: zaklyazminskaya ev. Front Physiol. 2021 Aug 4;12:716553. doi: 10.3389/fphys.2021.716553. eCollection 2021. Front Physiol. 2021. PMID: 34421659 Free PMC article. No abstract available.
Cardiac channelopathies: genetic and molecular mechanisms.
Abriel H, Zaklyazminskaya EV. Abriel H, et al. Among authors: zaklyazminskaya ev. Gene. 2013 Mar 15;517(1):1-11. doi: 10.1016/j.gene.2012.12.061. Epub 2012 Dec 22. Gene. 2013. PMID: 23266818 Review.
ISE/ISHNE Expert Consensus Statement on ECG Diagnosis of Left Ventricular Hypertrophy: The Change of the Paradigm. The joint paper of the International Society of Electrocardiology and the International Society for Holter Monitoring and Noninvasive Electrocardiology.
Bacharova L, Chevalier P, Gorenek B, Jons C, Li YG, Locati ET, Maanja M, Pérez-Riera AR, Platonov PG, Ribeiro ALP, Schocken D, Soliman EZ, Svehlikova J, Tereshchenko LG, Ugander M, Varma N, Zaklyazminskaya E, Ikeda T. Bacharova L, et al. Among authors: zaklyazminskaya e. J Electrocardiol. 2023 Nov-Dec;81:85-93. doi: 10.1016/j.jelectrocard.2023.08.005. Epub 2023 Aug 18. J Electrocardiol. 2023. PMID: 37647776 Review.
Clinical Classification of Arrhythmogenic Right Ventricular Cardiomyopathy.
Lutokhina Y, Blagova O, Nedostup A, Alexandrova S, Shestak A, Zaklyazminskaya E. Lutokhina Y, et al. Among authors: zaklyazminskaya e. Pulse (Basel). 2020 Aug;8(1-2):21-30. doi: 10.1159/000505652. Epub 2020 Feb 11. Pulse (Basel). 2020. PMID: 32999875 Free PMC article.
De Novo Asp219Val Mutation in Cardiac Tropomyosin Associated with Hypertrophic Cardiomyopathy.
Tsaturyan AK, Zaklyazminskaya EV, Polyak ME, Kopylova GV, Shchepkin DV, Kochurova AM, Gonchar AD, Kleymenov SY, Koubasova NA, Bershitsky SY, Matyushenko AM, Levitsky DI. Tsaturyan AK, et al. Among authors: zaklyazminskaya ev. Int J Mol Sci. 2022 Dec 20;24(1):18. doi: 10.3390/ijms24010018. Int J Mol Sci. 2022. PMID: 36613463 Free PMC article.
36 results