Sfoglia per Autore
Two cases of sudden unexpected death in epilepsy in a GEFS+ family with an SCN1A mutation.
2008-01-01 Hindocha, N; Nashef, L; Elmslie, F; Birch, R; Zuberi, S; Al Chalabi, A; Crotti, Lia; Schwartz, Peter; Makoff, A.
Ion channel diseases in children: manifestations and management.
2008-01-01 Schwartz, Peter; Crotti, Lia
Neural control of heart rate is an arrhythmia risk modifier in long QT syndrome.
2008-01-01 Schwartz, Peter; Vanoli, Emilio; Crotti, Lia; Spazzolini, Carla; Ferrandi, C; Goosen, A; Hedley, P; Heradien, M; Bacchini, S; Turco, A; La Rovere, Mt; Bartoli, A; George AL, Jr; Brink, Pa
Left cardiac sympathetic denervation for catecholaminergic polymorphic ventricular tachycardia
2008-01-01 Wilde, Aam; Bhuiyan, ; Crotti, Lia; Facchini, M; DE FERRARI, Gaetano; Paul, T; Ferrandi, C; Koolbergen, Dr; Odero, ATTILIO NICOLO'; Schwartz, Peter
Malignant perinatal variant of long-QT syndrome caused by a profoundly dysfunctional cardiac sodium channel.
2008-01-01 Wang, Dw; Crotti, Lia; Shimizu, W; Pedrazzini, M; Cantu, F; De Filippo, P; Kishiki, K; Miyazaki, A; Ikeda, T; Schwartz, Peter; George AL, Jr
Novel human pathological mutations. Gene symbol: SCN5A. Disease: Brugada Syndrome.
2009-01-01 Crotti, Lia; Pedrazzini, M; Insolia, Roberto; Cuoretti, A; Ghidoni, A; Dagradi, F; Taravelli, E; Chieffo, E; Vicentini, A; Schwartz, Peter
Clinical implications for patients with Long QT Syndrome who experience a cardiac event during infancy
2009-01-01 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.
Congenital long QT and short QT syndromes
2009-01-01 Schwartz, Peter; Crotti, Lia
Sindrome di Brugada
2009-01-01 Crotti, Lia; Schwartz, Peter
QT lungo, sindrome del
2009-01-01 Schwartz, Peter; Crotti, Lia
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”.
2009-01-01 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.
All LQT3 patients need an ICD. True or false?
2009-01-01 Schwartz, Peter; Spazzolini, C; Crotti, Lia
Prevalence of the congenital long-QT syndrome.
2009-01-01 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.
2009-01-01 Crotti, Lia; Lewandowska, Ma; Schwartz, Peter; Insolia, Roberto; Pedrazzini, M; Bussani, E; Dagradi, F; George AL, Jr; Pagani, F.
NOS1AP Is a Genetic Modifier of the Long-QT Syndrome
2009-01-01 Crotti, Lia; Monti, MARIA CRISTINA; Insolia, Roberto; Peljto, A; Goosen, A; Brink, Pa; Greenberg, Da; Schwartz, Peter; George, Al
Congenital Short QT Syndrome
2010-01-01 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
2010-01-01 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.
2010-01-01 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.
2010-01-01 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.
Ion channels and beating heart: the players and the music
2011-01-01 Crotti, Lia; Limongelli, G.; Antzelevitch, C.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Two cases of sudden unexpected death in epilepsy in a GEFS+ family with an SCN1A mutation. | 1-gen-2008 | Hindocha, N; Nashef, L; Elmslie, F; Birch, R; Zuberi, S; Al Chalabi, A; Crotti, Lia; Schwartz, Peter; Makoff, A. | |
Ion channel diseases in children: manifestations and management. | 1-gen-2008 | Schwartz, Peter; Crotti, Lia | |
Neural control of heart rate is an arrhythmia risk modifier in long QT syndrome. | 1-gen-2008 | Schwartz, Peter; Vanoli, Emilio; Crotti, Lia; Spazzolini, Carla; Ferrandi, C; Goosen, A; Hedley, P; Heradien, M; Bacchini, S; Turco, A; La Rovere, Mt; Bartoli, A; George AL, Jr; Brink, Pa | |
Left cardiac sympathetic denervation for catecholaminergic polymorphic ventricular tachycardia | 1-gen-2008 | Wilde, Aam; Bhuiyan, ; Crotti, Lia; Facchini, M; DE FERRARI, Gaetano; Paul, T; Ferrandi, C; Koolbergen, Dr; Odero, ATTILIO NICOLO'; Schwartz, Peter | |
Malignant perinatal variant of long-QT syndrome caused by a profoundly dysfunctional cardiac sodium channel. | 1-gen-2008 | Wang, Dw; Crotti, Lia; Shimizu, W; Pedrazzini, M; Cantu, F; De Filippo, P; Kishiki, K; Miyazaki, A; Ikeda, T; Schwartz, Peter; George AL, Jr | |
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 | |
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. | |
Congenital long QT and short QT syndromes | 1-gen-2009 | Schwartz, Peter; Crotti, Lia | |
Sindrome di Brugada | 1-gen-2009 | Crotti, Lia; Schwartz, Peter | |
QT lungo, sindrome del | 1-gen-2009 | Schwartz, Peter; Crotti, Lia | |
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. | |
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. | |
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 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. | |
Ion channels and beating heart: the players and the music | 1-gen-2011 | Crotti, Lia; Limongelli, G.; Antzelevitch, C. |
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