INSOLIA, ROBERTO

INSOLIA, ROBERTO  

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A KCNH2 branch point mutation causing aberrant splicing contributes to an explanation of genotype-negative long QT syndrome. 1-gen-2009 Crotti, Lia; Lewandowska, Ma; Schwartz, Peter; Insolia, Roberto; Pedrazzini, M; Bussani, E; Dagradi, F; George AL, Jr; Pagani, F.
Arrhythmogenic disorders of genetic origin. Long QT Syndrome: from genetics to management. 1-gen-2012 Schwartz, Peter; Crotti, Lia; Insolia, Roberto
Cardiac potassium channel dysfunction in sudden infant death syndrome. 1-gen-2008 Rhodes, Te; Abraham, Rl; Welch, Rc; Vanoye, Cg; Crotti, Lia; Arnestad, M; Insolia, Roberto; Pedrazzini, M; Ferrandi, C; Vege, A; Rognum, T; Roden, Dm; Schwartz, Peter; George AL, Jr
Cardiac sodium channel dysfunction in sudden infant death syndrome. 1-gen-2007 Wang, Dw; Desai, Rr; Crotti, Lia; Arnestad, M; Insolia, Roberto; Pedrazzini, M; Ferrandi, C; Vege, A; Rognum, T; Schwartz, Peter; George AL, Jr
Gene symbol: KCNH2 1-gen-2007 Crotti, Lia; Pedrazzini, M.; Ferrandi, C.; Insolia, Roberto; Tosin, L.; Vicentini, A.; Turco, A.; DE FERRARI, Gaetano; Schwartz, P. J.
Inherited cardiac arrhythmia syndrome. Role of potassium channels 1-gen-2011 Crotti, Lia; Insolia, Roberto; Schwartz, Peter
Inherited cardiac arrhythmia syndrome: Role of potassium channels. 1-gen-2011 Crotti, Lia; Insolia, Roberto; Schwartz, Peter
KCNH2-K897T Is a Genetic Modifier of Latent Congenital Long-QT Syndrome. 1-gen-2005 Crotti, Lia; Lundquist, Al; Insolia, Roberto; Pedrazzini, M; Ferrandi, C; DE FERRARI, Gaetano; Vicentini, A; Yang, P; Roden, Dm; George AL, Jr; Schwartz, Peter
KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome. 1-gen-2005 Crotti, Lia; Lundquist, Al; Insolia, Roberto; Pedrazzini, Matteo; Ferrandi, Chiara; DE FERRARI, Gaetano; Vicentini, Alessandro; Yang, P; Roden, Dm; George AL, Jr; Schwartz, Peter
Long QT syndrome-associated mutations in intrauterine fetal death. 1-gen-2013 Crotti, Lia; Tester, D. J.; White, W. M.; Bartos, D. C.; Insolia, Roberto; Besana, A.; Kunic, J. D.; Will, M. L.; Velasco, E. J.; Bair, J. J.; Ghidoni, Alice; Cetin, I.; Van Dyke, D. L.; Wick, M. J.; Brost, B.; Delisle, B. P.; Facchinetti, F.; George, A. L.; Schwartz, Peter; Ackerman, M. J.
NOS1AP Is a Genetic Modifier of the Long-QT Syndrome 1-gen-2009 Crotti, Lia; Monti, MARIA CRISTINA; Insolia, Roberto; Peljto, A; Goosen, A; Brink, Pa; Greenberg, Da; Schwartz, Peter; George, Al
Novel human pathological mutations. Gene symbol: SCN5A. Disease: Brugada Syndrome. 1-gen-2009 Crotti, Lia; Pedrazzini, M; Insolia, Roberto; Cuoretti, A; Ghidoni, A; Dagradi, F; Taravelli, E; Chieffo, E; Vicentini, A; Schwartz, Peter
PREDESTINATION: PRimary vEntricular fibrillation and suDden dEath during a firST myocardIal iNfArcTION: Genetic basis. 1-gen-2013 DE FERRARI, Gaetano; De Regibus, V; Gionti, V; Civardi, D; Insolia, Roberto; Pedrazzini, M; Gentilini, D; Di Blasio, A; Crotti, Lia; Schwartz, Peter
Prevalence of long-QT syndrome gene variants in sudden infant death syndrome. 1-gen-2007 Arnestad, M; Crotti, Lia; Rognum, To; Insolia, Roberto; Pedrazzini, M; Ferrandi, C; Vege, A; Wang, Dw; Rhodes, Te; George AL, Jr; Schwartz, Peter
Prevalence of the congenital long-QT syndrome. 1-gen-2009 Schwartz, Peter; Stramba Badiale, M; Crotti, Lia; Pedrazzini, M; Besana, A; Bosi, G; Gabbarini, F; Goulene, K; Insolia, Roberto; Mannarino, S; Mosca, F; Nespoli, L; Rimini, A; Rosati, E; Salice, P; Spazzolini, C.
Propranolol prevents life-threatening arrhythmias in LQT3 transgenic mice: implications for the clinical management of LQT3 patients. 1-gen-2014 Calvillo, L; Spazzolini, Carla; Vullo, Eleonora; Insolia, Roberto; Crotti, Lia; Schwartz, Peter
Torsades de Pointes following Acute Myocardial Infarction: Evidence for a Deadly Link with a Common Genetic Variant. 1-gen-2012 Crotti, Lia; Hu, D; Barajas Martinez, H; DE FERRARI, Gaetano; Oliva, A; Insolia, Roberto; Pollevick, Gd; Dagradi, Federica; Guerchicoff, A; Greco, F; Schwartz, Peter; Viskin, S; Antzelevitch, C.