Sfoglia per Autore
Idiopathic Ventricular Fibrillation.
1999-01-01 Priori, SILVIA GIULIANA; Crotti, Lia
Molecular basis of atrial fibrillation
1999-01-01 Priori, SILVIA GIULIANA; Crotti, Lia
Brugada and Long QT Syndrome are two different diseases: True or False?
1999-01-01 Priori, SILVIA GIULIANA; Crotti, Lia
The elusive link between LQT3 and Brugada syndrome: the role of flecainide challenge.
2000-01-01 Priori, SILVIA GIULIANA; Napolitano, C; Schwartz, Peter; Bloise, R; Crotti, Lia; Ronchetti, E.
Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 families.
2000-01-01 Priori, SILVIA GIULIANA; Napolitano, C; Gasparini, M; Pappone, C; Della Bella, P; Brignole, M; Giordano, U; Giovannini, T; Menozzi, C; Bloise, R; Crotti, Lia; Terreni, L; Schwartz, Peter
Idiopathic Ventricular Fibrillation
2000-01-01 Priori, SILVIA GIULIANA; Crotti, Lia
The Long QT Syndrome
2001-01-01 Priori, SILVIA GIULIANA; Bloise, R; Crotti, Lia
Long QT Syndrome and Brugada Syndrome : 2 aspects of the same disease ?
2001-01-01 Cerrone, M; Crotti, Lia; Faggiano, G; De Michelis, V; Napolitano, C; Schwartz, Peter; Priori, SILVIA GIULIANA
KCNH2-K897T Is a Genetic Modifier of Latent Congenital Long-QT Syndrome.
2005-01-01 Crotti, Lia; Lundquist, Al; Insolia, Roberto; Pedrazzini, M; Ferrandi, C; DE FERRARI, Gaetano; Vicentini, A; Yang, P; Roden, Dm; George AL, Jr; Schwartz, Peter
Phenotypic variability and unusual clinical severity of congenital long-QT syndrome in a founder population.
2005-01-01 Brink, Pa; Crotti, Lia; Corfield, V; Goosen, A; Durrheim, G; Hedley, P; Heradien, M; Geldenhuys, G; Vanoli, Emilio; Bacchini, S; Spazzolini, Carla; Lundquist, Al; Roden, Dm; George AL, Jr; Schwartz, Peter
KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome.
2005-01-01 Crotti, Lia; Lundquist, Al; Insolia, Roberto; Pedrazzini, Matteo; Ferrandi, Chiara; DE FERRARI, Gaetano; Vicentini, Alessandro; Yang, P; Roden, Dm; George AL, Jr; Schwartz, Peter
Does pregnancy increase cardiac risk for LQT1 patients with the KCNQ1-A341V mutation?
2006-01-01 Heradien, Mj; Goosen, A; Crotti, Lia; Durrheim, G; Corfield, V; Brink, Pa; Schwartz, Peter
The Jervell and Lange-Nielsen syndrome: natural history, molecular basis, and clinical outcome.
2006-01-01 Schwartz, Peter; Spazzolini, C; Crotti, Lia; Bathen, J; Amlie, Jp; Timothy, K; Shkolnikova, M; Berul, Ci; Bitner Glindzicz, M; Toivonen, L; Horie, M; Schulze Bahr, E; Denjoy, I.
Individual autonomic profile contributes to the risk for life-threatening arrhythmias among KCNQ1-A341V mutation carriers
2006-01-01 Vanoli, Emilio; Crotti, Lia; Schwartz, Peter; Heradien, M; Spazzolini, C; La Rovere, Mt; Bacchini, S; Goosen, A; Brink, Pa; George, A. l. J.
The ICD for the long QT syndrome: which indications, complications, and results?
2006-01-01 Schwartz, Peter; Spazzolini, C; Crotti, Lia
Prevalence of long QT syndrome gene variants in sudden infant death syndrome.
2006-01-01 Arnestad, M; Crotti, Lia; Rognum, To; Insolia, R; Pedrazzini, M; Ferrandi, C; Vege, A; Schwartz, Peter
The Common Long QT Syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratification.
2007-01-01 Crotti, Lia; Spazzolini, C.; Schwartz, Peter; Shimizu, W.; Denjoy, I.; Schulze Bahr, E.; Zaklyazminskaya, E. v.; Swan, H. .; Ackerman M., J; Moss, A. j.; Wilde, A.; Horie, M.; Brink, P. a.; Insolita, R.; DE FERRARI, Gaetano; Crimi, G.
Cardiac arrhythmias of genetic origin are important contributors to Sudden Infant Death Syndrome.
2007-01-01 Schwartz, Peter; Crotti, Lia
Can a message from the dead save lives?
2007-01-01 Schwartz, Peter; Crotti, Lia
Prevalence of long-QT syndrome gene variants in sudden infant death syndrome.
2007-01-01 Arnestad, M; Crotti, Lia; Rognum, To; Insolia, Roberto; Pedrazzini, M; Ferrandi, C; Vege, A; Wang, Dw; Rhodes, Te; George AL, Jr; Schwartz, Peter
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Idiopathic Ventricular Fibrillation. | 1-gen-1999 | Priori, SILVIA GIULIANA; Crotti, Lia | |
Molecular basis of atrial fibrillation | 1-gen-1999 | Priori, SILVIA GIULIANA; Crotti, Lia | |
Brugada and Long QT Syndrome are two different diseases: True or False? | 1-gen-1999 | Priori, SILVIA GIULIANA; Crotti, Lia | |
The elusive link between LQT3 and Brugada syndrome: the role of flecainide challenge. | 1-gen-2000 | Priori, SILVIA GIULIANA; Napolitano, C; Schwartz, Peter; Bloise, R; Crotti, Lia; Ronchetti, E. | |
Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 families. | 1-gen-2000 | Priori, SILVIA GIULIANA; Napolitano, C; Gasparini, M; Pappone, C; Della Bella, P; Brignole, M; Giordano, U; Giovannini, T; Menozzi, C; Bloise, R; Crotti, Lia; Terreni, L; Schwartz, Peter | |
Idiopathic Ventricular Fibrillation | 1-gen-2000 | Priori, SILVIA GIULIANA; Crotti, Lia | |
The Long QT Syndrome | 1-gen-2001 | Priori, SILVIA GIULIANA; Bloise, R; Crotti, Lia | |
Long QT Syndrome and Brugada Syndrome : 2 aspects of the same disease ? | 1-gen-2001 | Cerrone, M; Crotti, Lia; Faggiano, G; De Michelis, V; Napolitano, C; Schwartz, Peter; Priori, SILVIA GIULIANA | |
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 | |
Phenotypic variability and unusual clinical severity of congenital long-QT syndrome in a founder population. | 1-gen-2005 | Brink, Pa; Crotti, Lia; Corfield, V; Goosen, A; Durrheim, G; Hedley, P; Heradien, M; Geldenhuys, G; Vanoli, Emilio; Bacchini, S; Spazzolini, Carla; Lundquist, Al; 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 | |
Does pregnancy increase cardiac risk for LQT1 patients with the KCNQ1-A341V mutation? | 1-gen-2006 | Heradien, Mj; Goosen, A; Crotti, Lia; Durrheim, G; Corfield, V; Brink, Pa; Schwartz, Peter | |
The Jervell and Lange-Nielsen syndrome: natural history, molecular basis, and clinical outcome. | 1-gen-2006 | Schwartz, Peter; Spazzolini, C; Crotti, Lia; Bathen, J; Amlie, Jp; Timothy, K; Shkolnikova, M; Berul, Ci; Bitner Glindzicz, M; Toivonen, L; Horie, M; Schulze Bahr, E; Denjoy, I. | |
Individual autonomic profile contributes to the risk for life-threatening arrhythmias among KCNQ1-A341V mutation carriers | 1-gen-2006 | Vanoli, Emilio; Crotti, Lia; Schwartz, Peter; Heradien, M; Spazzolini, C; La Rovere, Mt; Bacchini, S; Goosen, A; Brink, Pa; George, A. l. J. | |
The ICD for the long QT syndrome: which indications, complications, and results? | 1-gen-2006 | Schwartz, Peter; Spazzolini, C; Crotti, Lia | |
Prevalence of long QT syndrome gene variants in sudden infant death syndrome. | 1-gen-2006 | Arnestad, M; Crotti, Lia; Rognum, To; Insolia, R; Pedrazzini, M; Ferrandi, C; Vege, A; Schwartz, Peter | |
The Common Long QT Syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratification. | 1-gen-2007 | Crotti, Lia; Spazzolini, C.; Schwartz, Peter; Shimizu, W.; Denjoy, I.; Schulze Bahr, E.; Zaklyazminskaya, E. v.; Swan, H. .; Ackerman M., J; Moss, A. j.; Wilde, A.; Horie, M.; Brink, P. a.; Insolita, R.; DE FERRARI, Gaetano; Crimi, G. | |
Cardiac arrhythmias of genetic origin are important contributors to Sudden Infant Death Syndrome. | 1-gen-2007 | Schwartz, Peter; Crotti, Lia | |
Can a message from the dead save lives? | 1-gen-2007 | Schwartz, Peter; Crotti, Lia | |
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 |
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