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Journal Abstract Search

114 related items for PubMed ID: 34892380

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  • 3. De Novo Mutation in the SCN5A Gene Associated with Brugada Syndrome.
    Wang L, Meng X, Yuchi Z, Zhao Z, Xu D, Fedida D, Wang Z, Huang C.
    Cell Physiol Biochem; 2015; 36(6):2250-62. PubMed ID: 26279430
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  • 4. A heterozygous deletion mutation in the cardiac sodium channel gene SCN5A with loss- and gain-of-function characteristics manifests as isolated conduction disease, without signs of Brugada or long QT syndrome.
    Zumhagen S, Veldkamp MW, Stallmeyer B, Baartscheer A, Eckardt L, Paul M, Remme CA, Bhuiyan ZA, Bezzina CR, Schulze-Bahr E.
    PLoS One; 2013; 8(6):e67963. PubMed ID: 23840796
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  • 8. Brugada syndrome: clinical presentation and genotype-correlation with magnetic resonance imaging parameters.
    Rudic B, Schimpf R, Veltmann C, Doesch C, Tülümen E, Schoenberg SO, Borggrefe M, Papavassiliu T.
    Europace; 2016 Sep; 18(9):1411-9. PubMed ID: 26511399
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  • 9. Single-cell transcriptomics trajectory and molecular convergence of clinically relevant mutations in Brugada syndrome.
    Tambi R, Abdel Hameid R, Bankapur A, Nassir N, Begum G, Alsheikh-Ali A, Uddin M, Berdiev BK.
    Am J Physiol Heart Circ Physiol; 2021 May 01; 320(5):H1935-H1948. PubMed ID: 33797273
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  • 11. [Genetic and molecular basis for sodium channel-mediated Brugada syndrome].
    Barajas-Martínez H, Hu D, Antzelevitch C.
    Arch Cardiol Mex; 2013 May 01; 83(4):295-302. PubMed ID: 24269159
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  • 13. Concomitant Brugada-like and short QT electrocardiogram linked to SCN5A mutation.
    Hong K, Hu J, Yu J, Brugada R.
    Eur J Hum Genet; 2012 Nov 01; 20(11):1189-92. PubMed ID: 22490985
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  • 14. Genetic mutation in Korean patients of sudden cardiac arrest as a surrogating marker of idiopathic ventricular arrhythmia.
    Son MK, Ki CS, Park SJ, Huh J, Kim JS, On YK.
    J Korean Med Sci; 2013 Jul 01; 28(7):1021-6. PubMed ID: 23853484
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  • 15. Functional Characterization of Two Novel Mutations in SCN5A Associated with Brugada Syndrome Identified in Italian Patients.
    Balla C, Conte E, Selvatici R, Marsano RM, Gerbino A, Farnè M, Blunck R, Vitali F, Armaroli A, Brieda A, Liantonio A, De Luca A, Ferlini A, Rapezzi C, Bertini M, Gualandi F, Imbrici P.
    Int J Mol Sci; 2021 Jun 17; 22(12):. PubMed ID: 34204499
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  • 18. Electrophysiological and trafficking defects of the SCN5A T353I mutation in Brugada syndrome are rescued by alpha-allocryptopine.
    Zhang J, Chen Y, Yang J, Xu B, Wen Y, Xiang G, Wei G, Zhu C, Xing Y, Li Y.
    Eur J Pharmacol; 2015 Jan 05; 746():333-43. PubMed ID: 25261036
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  • 19. A sodium channel pore mutation causing Brugada syndrome.
    Pfahnl AE, Viswanathan PC, Weiss R, Shang LL, Sanyal S, Shusterman V, Kornblit C, London B, Dudley SC.
    Heart Rhythm; 2007 Jan 05; 4(1):46-53. PubMed ID: 17198989
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  • 20. SCN1B gene variants in Brugada Syndrome: a study of 145 SCN5A-negative patients.
    Ricci MT, Menegon S, Vatrano S, Mandrile G, Cerrato N, Carvalho P, De Marchi M, Gaita F, Giustetto C, Giachino DF.
    Sci Rep; 2014 Sep 25; 4():6470. PubMed ID: 25253298
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