PuSH - Publication Server of Helmholtz Zentrum München

36 Records found.
Zum Exportieren der Ergebnisse bitte einloggen.
Lay all publications on this page into basket
Empana, J.P.* et al.: Determinants of occurrence and survival after sudden cardiac arrest–A European perspective: The ESCAPE-NET project. Resuscitation 124, 7-13 (2018)
Mayosi, B.M.* et al.: Identification of cadherin 2 (CDH2) mutations in arrhythmogenic right ventricular cardiomyopathy. Circ. Cardiovasc. Genet. 10:e001605 (2017)
Crotti, L.* et al.: Genetic modifiers for the long-QT syndrome: How important Is the role of variants in the 3' untranslated region of KCNQ1? Circ. Cardiovasc. Genet. 9, 330-339 (2016)
Crotti, L.* et al.: Response by Crotti et al to letter regarding article, "Genetic modifiers for the long-QT syndrome: How important is the role of variants in the 3 ' untranslated region of KCNQ1?" Circ. Cardiovasc. Genet. 9, 581-582 (2016)
Itoh, H.* et al.: The genetics underlying acquired long QT syndrome: Impact for genetic screening. Eur. Heart J. 37, 1456-1464 (2016)
Wilde, A.A.* et al.: Clinical aspects of type 3 long QT syndrome: An international multicenter study. Circulation 134, 872-882 (2016)
Bari, V.* et al.: A refined multiscale self-entropy approach for the assessment of cardiac control complexity: Application to long QT syndrome type 1 patients. Entropy 17, 7768-7785 (2015)
Bari, V.* et al.: Time, frequency and information domain analysis of heart period and QT variability in asymptomatic long QT syndrome type 2 patients. In: (37th Annual International Conference of the IEEE Engineering in Medicine and Biology Society, EMBC 2015, 25-29 August 2015, Milan, Italy). 2015. 294-297 (Conf. Proc. IEEE Eng. Med. Biol. Soc. ; 2015)
de Ferrari, G.M.* et al.: Clinical management of catecholaminergic polymorphic ventricular tachycardia: The role of left cardiac sympathetic denervation. Circulation 131, 2185-2193 (2015)
Porta, A.* et al.: Autonomic control of heart rate and QT interval variability influences arrhythmic risk in long QT syndrome type 1. J. Am. Coll. Cardiol. 65, 367-374 (2015)
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)
Bari, V.* et al.: Symbolic analysis of heart period and QT interval variabilities in LQT1 patients. IFMBE Proc. 41, 531-534 (2014)
Bari, V.* et al.: Multiscale complexity analysis of the cardiac control identifies asymptomatic and symptomatic patients in long QT syndrome type 1. PLoS ONE 9:e93808 (2014)
Bari, V.* et al.: Low-pass filtering approach via empirical mode decomposition improves short-scale entropy-based complexity estimation of QT interval variability in long QT syndrome type 1 patients. Entropy 16, 4839-4854 (2014)
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)
Calvillo, L.* et al.: Propranolol prevents life-threatening arrhythmias in LQT3 transgenic mice: Implications for the clinical management of LQT3 patients. Heart Rhythm 11, 126-132 (2014)
Crotti, L. & Schwartz, P.J.*: Drug-induced long QT syndrome and exome sequencing: Chinese shadows link past and future. J. Am. Coll. Cardiol. 63, 1438–1440 (2014)
Crotti, L. ; Ghidoni, A.* ; Insolia, R.* & Schwartz, P.J.*: The role of the cardiac sodium channel in perinatal early infant mortality. Card. Electrophysiol. Clin. 6, 749-759 (2014)
de Villiers, C.P.* et al.: AKAP9 is a genetic modifier of congenital long-QT syndrome type 1. Circ. Cardiovasc. Genet. 7, 599-606 (2014)
Makita, N.* et al.: Novel calmodulin (CALM2) mutations associated with congenital arrhythmia susceptibility. Circ. Cardiovasc. Genet. 7, 466-474 (2014)