CROTTI, LIA
CROTTI, LIA
DIPARTIMENTO DI MEDICINA E CHIRURGIA (SCHOOL OF MEDICINE AND SURGERY)
Brugada and Long QT Syndrome are two different diseases: True or False?
1999 Priori, S; Crotti, L
Idiopathic Ventricular Fibrillation
1999 Priori, S; Crotti, L
Idiopathic Ventricular Fibrillation
2000 Priori, S; Crotti, L
Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 families
2000 Priori, S; Napolitano, C; Gasparini, M; Pappone, C; Della Bella, P; Brignole, M; Giordano, U; Giovannini, T; Menozzi, C; Bloise, R; Crotti, L; Terreni, L; Schwartz, P
The elusive link between LQT3 and Brugada syndrome: the role of flecainide challenge
2000 Priori, S; Napolitano, C; Schwartz, P; Bloise, R; Crotti, L; Ronchetti, E
The Long QT Syndrome
2001 Priori, S; Bloise, R; Crotti, L
Long QT Syndrome and Brugada Syndrome : 2 aspects of the same disease?
2001 Cerrone, M; Crotti, L; Faggiano, G; De Michelis, V; Napolitano, C; Schwartz, P; Priori, S
Phenotypic variability and unusual clinical severity of congenital long-QT syndrome in a founder population
2005 Brink, P; Crotti, L; Corfield, V; Goosen, A; Durrheim, G; Hedley, P; Heradien, M; Geldenhuys, G; Vanoli, E; Bacchini, S; Spazzolini, C; Lundquist, A; Roden, D; George AL, J; Schwartz, P
KCNH2-K897T Is a Genetic Modifier of Latent Congenital Long-QT Syndrome
2005 Crotti, L; Lundquist, A; Insolia, R; Pedrazzini, M; Ferrandi, C; De Ferrari, G; Vicentini, A; Yang, P; Roden, D; George AL, J; Schwartz, P
The ICD for the long QT syndrome: which indications, complications, and results?
2005 Schwartz, P; Spazzolini, C; Crotti, L
The Jervell and Lange-Nielsen syndrome: natural history, molecular basis, and clinical outcome
2006 Schwartz, P; Spazzolini, C; Crotti, L; Bathen, J; Amlie, J; Timothy, K; Shkolnikova, M; Berul, C; Bitner-Glindzicz, M; Toivonen, L; Horie, M; Schulze-Bahr, E; Denjoy, I
Does pregnancy increase cardiac risk for LQT1 patients with the KCNQ1-A341V mutation?
2006 Heradien, M; Goosen, A; Crotti, L; Durrheim, G; Corfield, V; Brink, P; Schwartz, P
Gene symbol: SCN5A. Disease: Long QT syndrome in Novel human pathological mutations
2007 Crotti, L; Ferrandi, C; Insolia, R; Pedrazzini, M; Andreoli, E; Veia, A; Crimi, G; Agnetti, A; De Ferrari, G; Schwartz, P
Gene symbol: KCNQ1. Disease: Long QT syndrome
2007 Crotti, L; Insolia, R; Pedrazzini, M; Ferrandi, C; Tosin, L; Moncalvo, C; Turco, A; Agnetti, A; De Ferrari, G; Schwartz, P
Cardiac sodium channel dysfunction in sudden infant death syndrome
2007 Wang, D; Desai, R; Crotti, L; Arnestad, M; Insolia, R; Pedrazzini, M; Ferrandi, C; Vege, A; Rognum, T; Schwartz, P; George AL, J
Cardiac arrhythmias of genetic origin are important contributors to Sudden Infant Death Syndrome
2007 Schwartz, P; Crotti, L
Gene symbol: SCN5A. Disease: Long QT syndrome in Novel human pathological mutations
2007 Crotti, L; Ferrandi, C; Insolia, R; Pedrazzini, M; Tosin, L; Veia, A; Turco, A; De Ferrari, G; Schwartz, P
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 Crotti, L; Spazzolini, C; Schwartz, P; Shimizu, W; Denjoy, I; Schulze-Bahr, E; Zaklyazminskaya, E; Swan, H; Ackerman M., J; Moss, A; Wilde, A; Horie, M; Brink, P; Insolia, R; De Ferrari, G; Crimi, G
Gene Symbol: KCNH2 Disease: Long QT syndrome
2007 Crotti, L; Pedrazzini, M; Ferrandi, C; Insolia, R; Tosin, L; Vicentini, A; Turco, A; De Ferrari, G; Schwartz, P
Can a message from the dead save lives?
2007 Schwartz, P; Crotti, L