PuSH - Publication Server of Helmholtz Zentrum München

8 Records found.
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1.
Wilde, A.A.* et al.: Clinical aspects of type 3 long QT syndrome: An international multicenter study. Circulation 134, 872-882 (2016)
2.
Arking, D.E.* et al.: Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. Nat. Genet. 46, 826-836 (2014)
3.
Boczek, N.J.* et al.: Characterization of SEMA3A-encoded semaphorin as a naturally occurring Kv4.3 protein inhibitor and its contribution to Brugada syndrome. Circ. Res. 115, 460-469 (2014)
4.
Crotti, L. et al.: Long QT syndrome-associated mutations in intrauterine fetal death. JAMA 309, 1473-1482 (2013)
5.
Hennessey, J.A.* et al.: FGF12 is a candidate Brugada syndrome locus. Heart Rhythm 10, 1886-1894 (2013)
6.
Crotti, L. et al.: Spectrum and prevalence of mutations involving BrS1- through BrS12-susceptibility genes in a cohort of unrelated patients referred for Brugada Syndrome genetic testing: Implications for genetic testing. J. Am. Coll. Cardiol. 60, 1410-1418 (2012)
7.
Hu, D.* et al.: A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Nav1.5 and Kv4.3 channel currents. Heart Rhythm 9, 760-769 (2012)
8.
Ishikawa, T.* et al.: A novel disease gene for Brugada syndrome: Sarcolemmal membrane-associated protein gene mutations impair intracellular trafficking of hNav1.5. Circ.-Arrhythmia Electrophysiol. 5, 1098-1107 (2012)