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Titolo Data di pubblicazione Autore(i) File
Gene symbol: SCN5A. 1-gen-2008 Crotti, Lia; Ferrandi, C; Pedrazzini, M; Insolia, R; Cuoretti, A; Sanzo, A; Dagradi, F; DE FERRARI, Gaetano; Schwartz, Peter
Gene symbol: KCNH2 1-gen-2008 Crotti, Lia; Pedrazzini, M; Ferrandi, C; Insolia, R; Cuoretti, A; Dagradi, F; Crimi, G; Coto, E; Reguero, Jr; Schwartz, Peter
Gene symbol: KCNQ1. 1-gen-2008 Crotti, Lia; Insolia, R; Ferrandi, C; Pedrazzini, M; Cuoretti, A; Gandolfi, E; Sanzo, A; Dagradi, F; Schwartz, Peter
Functional characterization and molecular correction of the LQT2 KCNH2-Q376 splicing mutation. Therapeutic implications? 1-gen-2008 Crotti, Lia; Lewandowska, M; Pedrazzini, M; Insolia, R; Ferrandi, C; Cuoretti, A; Bussani, E; Pagani, F; Schwartz, Peter
Gene symbol: KCNQ1. 1-gen-2008 Crotti, Lia; Ferrandi, C; Pedrazzini, M; Insolia, R; Cuoretti, A; Celano, G; Dagradi, F; Stramba Badiale, M; Schwartz, Peter
High efficacy of beta-blockers in Long QT Syndrome type 1: contribution of non-compliance and QT-prolonging drugs to the occurrence of beta-blocker treatment “failures”. 1-gen-2009 Vincent, Gm; Schwartz, Peter; Denjoy, I; Swan, H; Bithell, C; Spazzolini, C; Crotti, Lia; Piippo, K; Lupoglazoff, Jm; Villain, E; Priori, SILVIA GIULIANA; Napolitano, C; Zhang, L.
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
All LQT3 patients need an ICD. True or false? 1-gen-2009 Schwartz, Peter; Spazzolini, C; Crotti, Lia
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.
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.
Sindrome di Brugada 1-gen-2009 Crotti, Lia; Schwartz, Peter
QT lungo, sindrome del 1-gen-2009 Schwartz, Peter; Crotti, Lia
Clinical implications for patients with Long QT Syndrome who experience a cardiac event during infancy 1-gen-2009 Spazzolini, C; Mullally, J; Schwartz, Peter; Moss, Aj; Mcnitt, S; Ouellet, G; Fugate, T; Goldenberg, I; Jons, C; Zareba, W; Robinson, Jl; Ackerman, Mj; Benhorin, J; Crotti, Lia; Kaufman, Es; Locati, Eh; Ming, Q; Napolitano, C; Priori, SILVIA GIULIANA; Towbin, Ja; Vincent, G. M.
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
Congenital long QT and short QT syndromes 1-gen-2009 Schwartz, Peter; Crotti, Lia
Congenital Short QT Syndrome 1-gen-2010 Crotti, Lia; Taravelli, E; Girardengo, G; Schwartz, Peter
Gain of function mutation, S422L, in the KCNJ8-encoded cardiac K ATP channel Kir6.1 as a pathogenic substrate for J wave syndromes 1-gen-2010 Medeiros Domingo, A; Tan, Bh; Crotti, Lia; Tester, Dj; Eckhardt, L; Cuoretti, A; Kroboth, Sl; Song, C; Zhou, Q; Kopp, D; Schwartz, Peter; Makielski, Jc; Ackerman, M. J.
Who are the long-QT syndrome patients who receive an implantable cardioverter-defibrillator and what happens to them?: data from the European Long-QT Syndrome Implantable Cardioverter-Defibrillator (LQTS ICD) Registry. 1-gen-2010 Schwartz, Peter; Spazzolini, C; Priori, SILVIA GIULIANA; Crotti, Lia; Vicentini, A; Landolina, M; Gasparini, M; Wilde, Aa; Knops, Re; Denjoy, I; Toivonen, L; Mönnig, G; Al Fayyadh, M; Jordaens, L; Borggrefe, M; Holmgren, C; Brugada, P; De Roy, L; Hohnloser, Sh; Brink, P. A.
Mutation-specific risk in two genetic forms of type 3 long QT syndrome. 1-gen-2010 Liu, Jf; Moss, Aj; Jons, C; Benhorin, J; Schwartz, Peter; Spazzolini, C; Crotti, Lia; Ackerman, Mj; Mcnitt, S; Robinson, Jl; Qi, M; Goldenberg, I; Zareba, W.
Inherited cardiac arrhythmia syndrome. Role of potassium channels 1-gen-2011 Crotti, Lia; Insolia, Roberto; Schwartz, Peter
Mostrati risultati da 41 a 60 di 144
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