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Gene-specific response of dynamic ventricular repolarization to sympathetic stimulation in LQT1, LQT2 and LQT3 forms of congenital long QT syndrome 1-gen-2002 Noda, T; Takaki, H; Kurita, T; Suyama, K; Nagaya, N; Taguchi, A; Aihara, N; Kamakura, S; Sunagawa, K; Nakamura, K; Ohe, T; Horie, M; Napolitano, C; Towbin, Ja; Priori, SILVIA GIULIANA; Shimizu, W.
BRUGADA SYNDROME AND CONDUCTION SYSTEM DISEASE ARE LINKED TO A SINGLE SODIUM CHANNEL MUTATION. 1-gen-2002 Grant, Ao; Carboni, Mp; Neplioueva, V; Starmer, Cf; Memmi, M; Napolitano, C; Priori, SILVIA GIULIANA
La tachicardia ventricolare polimorfa catecolaminergica 1-gen-2003 Bloise, Raffaella; Moncalvo, C; Napolitano, C; Priori, SILVIA GIULIANA
Morte Improvvisa: dimensioni del problema, cause e meccanismi. 1-gen-2003 Priori, SILVIA GIULIANA; Napolitano, C; Grillo, M.
Epinephrine unmasks latent mutation carriers with LQT1 form of congenital long-QT syndrome. 1-gen-2003 Shimizu, W; Noda, T; Takaki, H; Kurita, T; Nagaya, N; Satomi, K; Suyama, K; Aihara, N; Kamakura, S; Sunagawa, K; Echigo, S; Nakamura, K; Ohe, T; Towbin, Ja; Napolitano, C; Priori, SILVIA GIULIANA
Risk stratification in the Long-QT Syndrome 1-gen-2003 Priori, SILVIA GIULIANA; Schwartz, Peter; Napolitano, C.; Bloise, R.; Grillo, M.; Vicentini, A.; Spazzolini, Carla; Ronchetti, E.; Cappelletti, D.; Nastoli, J.; Bottelli, G.; Folli, R.
Location of mutation in the KCNQ1 and phenotypic presentation of long QT syndrome. 1-gen-2003 Zareba, W.; Moss, A. J.; Sheu, G.; Kaufman, E. S.; Priori, SILVIA GIULIANA; Vincent, G. M.; Towbin, J. A.; Benhorin, J.; Schwartz, Peter; Napolitano, C.; Hall, W. J.; Keating, M. T.; Qi, M.; Robinson, J. L.; Andrews, M. L.
FKBP12.6 deficiency and defective calcium release channel (ryanodine receptor) function linked to exercise-induced sudden cardiac death. 1-gen-2003 Wehrens, Xh; Lehnart, Se; Huang, F; Vest, Ja; Reiken, Sr; Mohler, Pj; Sun, J; Guatimosim, S; Song, Ls; Rosemblit, N; D'Armiento, Jm; Napolitano, C; Memmi, M; Priori, SILVIA GIULIANA; Lederer, Wj; Marks, Ar
Inherited arrhythmia syndromes: applying the molecular biology and genetic to the clinical management. 1-gen-2003 Priori, SILVIA GIULIANA; Napolitano, C; Vicentini, A.
Modulating effects of age and gender on the clinical course of long QT syndrome by genotype. 1-gen-2003 Zareba, W; Moss, Aj; Locati, Eh; Lehmann, Mh; Peterson, Dr; Hall, Wj; Schwartz, Peter; Vincent, Gm; Priori, SILVIA GIULIANA; Benhorin, J; Towbin, Ja; Robinson, Jl; Andrews, Ml; Napolitano, C; Timothy, K; Zhang, L; Medina, A; International Long QT Syndrome, Registry
A newly charactarized SCN5A mutation underlying Brugada Syndrome unmasked by Hyperthermia 1-gen-2003 Mok, N. S.; Priori, SILVIA GIULIANA; Napolitano, C; Chan, N. Y.; Chahine, M; Boroudi, G.
Modulating effects of age and gender on the clinical course of long QT syndrome by genotype 1-gen-2003 Zareba, W; Moss, Aj; Locati, Eh; Lehmann, Mh; Peterson, Dr; Hall, Wj; Schwartz, Peter; Vincent, Gm; Priori, SILVIA GIULIANA; Benhorin, J; Towbin, Ja; Robinson, Jl; Andrews, Ml; Napolitano, C; Timothy, K; Zhang, L; Medina, A; International Long QT Syndrome, Registry
Flecainide test in Brugada Syndrome: a reproducible but risky tool 1-gen-2003 Gasparini, M; Priori, SILVIA GIULIANA; Mantica, M; Napolitano, C; Galimberti, P; Ceriotti, C; Simonini, S.
Cardiac Sodium Channel Diseases 1-gen-2003 Napolitano, C.; Rivolta, I.; Priori, SILVIA GIULIANA
Long QT Syndrome 1-gen-2004 Napolitano, C; Priori, SILVIA GIULIANA
Catecholaminergic Polymorphic Ventricular Tachycardia and Short-coupled Torsades de Pointes 1-gen-2004 Napolitano, C; Priori, SILVIA GIULIANA
Evaluation of BLS-D training in lay people. 1-gen-2004 Santomauro, M; Ottaviano, L; Borrelli, A; Riganti, C; Priori, SILVIA GIULIANA; Napolitano, C; Chiariello, M.
Genetic of Long QT, Brugada and Other Channelopathies 1-gen-2004 Priori, SILVIA GIULIANA; Rivolta, R; Napolitano, C.
ESC-ERC recommendations for the use of automated external defibrillators (AEDs) in Europe 1-gen-2004 Priori, SILVIA GIULIANA; Bossaert, L. L.; Chamberlain, D. A.; Napolitano, C.; Arntz, H. R.; Koster, R. W.; Monsieurs, K. G.; Capucci, A.; Wellens, H. J.
Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism 1-gen-2004 Splawski, I.; Timothy, K. W.; Sharpe, L. M.; Decher, N.; Kumar, P.; Bloise, R.; Napolitano, C.; Schwartz, Peter; Joseph, R. M.; Condouris, K.; TAGER FLUSBERG, H.; Priori, SILVIA GIULIANA; Sanguinetti, M. C.; Keating, M. T.
Mostrati risultati da 61 a 80 di 241
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