Sfoglia per Autore
Natural History of Brugada Syndrome: Insights for risk stratification and management
2002-01-01 Priori, SILVIA GIULIANA; Napolitano, C; Gasparini, M; Pappone, C; DELLA BELLA, P; Giordano, U; Bloise, Raffaella; Giustetto, C; DE NARDIS, R; Grillo, M; Ronchetti, E.
Romano-Ward and other congenital long QT syndromes
2002-01-01 Bloise, Raffaella; Napolitano, C; Priori, SILVIA GIULIANA
La tachicardia ventricolare polimorfa catecolaminergica
2003-01-01 Bloise, Raffaella; Moncalvo, C; Napolitano, C; Priori, SILVIA GIULIANA
Morte Improvvisa: dimensioni del problema, cause e meccanismi.
2003-01-01 Priori, SILVIA GIULIANA; Napolitano, C; Grillo, M.
Flecainide test in Brugada Syndrome: a reproducible but risky tool
2003-01-01 Gasparini, M; Priori, SILVIA GIULIANA; Mantica, M; Napolitano, C; Galimberti, P; Ceriotti, C; Simonini, S.
A newly charactarized SCN5A mutation underlying Brugada Syndrome unmasked by Hyperthermia
2003-01-01 Mok, N. S.; Priori, SILVIA GIULIANA; Napolitano, C; Chan, N. Y.; Chahine, M; Boroudi, G.
Epinephrine unmasks latent mutation carriers with LQT1 form of congenital long-QT syndrome.
2003-01-01 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
Cardiac Sodium Channel Diseases
2003-01-01 Napolitano, C.; Rivolta, I.; Priori, SILVIA GIULIANA
Location of mutation in the KCNQ1 and phenotypic presentation of long QT syndrome.
2003-01-01 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.
2003-01-01 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.
2003-01-01 Priori, SILVIA GIULIANA; Napolitano, C; Vicentini, A.
Modulating effects of age and gender on the clinical course of long QT syndrome by genotype
2003-01-01 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
Modulating effects of age and gender on the clinical course of long QT syndrome by genotype.
2003-01-01 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
Risk stratification in the Long-QT Syndrome
2003-01-01 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.
Long QT Syndrome
2004-01-01 Napolitano, C; Priori, SILVIA GIULIANA
Genetics of Cardiac Arrhythmias
2004-01-01 Priori, SILVIA GIULIANA; Napolitano, C; Schwartz, Peter
Clinical profile and genetic basis of Brugada syndrome in the Chinese population.
2004-01-01 Mok, Ns; Priori, SILVIA GIULIANA; Napolitano, C; Chan, Kk; Bloise, Raffaella; Chan, Hw; Fung, Wh; Chan, Ys; Chan, Wk; Lam, C; Chan, Ny; Tsang, H. H.
Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism
2004-01-01 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.
Genetics of cardiac arrhythmias and sudden cardiac death.
2004-01-01 Priori, SILVIA GIULIANA; Napolitano, C.
Nav1.5 E1053K mutation causing Brugada syndrome blocks binding to ankyrin-G and expression of Nav1.5 on the surface of cardiomyocytes.
2004-01-01 Mohler, P. J.; Rivolta, I.; Napolitano, C.; Lemaillet, G.; Lambert, S.; Priori, SILVIA GIULIANA; Bennett, V.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Natural History of Brugada Syndrome: Insights for risk stratification and management | 1-gen-2002 | Priori, SILVIA GIULIANA; Napolitano, C; Gasparini, M; Pappone, C; DELLA BELLA, P; Giordano, U; Bloise, Raffaella; Giustetto, C; DE NARDIS, R; Grillo, M; Ronchetti, E. | |
Romano-Ward and other congenital long QT syndromes | 1-gen-2002 | Bloise, Raffaella; 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. | |
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. | |
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. | |
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 | |
Cardiac Sodium Channel Diseases | 1-gen-2003 | Napolitano, C.; Rivolta, I.; Priori, SILVIA GIULIANA | |
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 | |
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 | |
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. | |
Long QT Syndrome | 1-gen-2004 | Napolitano, C; Priori, SILVIA GIULIANA | |
Genetics of Cardiac Arrhythmias | 1-gen-2004 | Priori, SILVIA GIULIANA; Napolitano, C; Schwartz, Peter | |
Clinical profile and genetic basis of Brugada syndrome in the Chinese population. | 1-gen-2004 | Mok, Ns; Priori, SILVIA GIULIANA; Napolitano, C; Chan, Kk; Bloise, Raffaella; Chan, Hw; Fung, Wh; Chan, Ys; Chan, Wk; Lam, C; Chan, Ny; Tsang, H. H. | |
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. | |
Genetics of cardiac arrhythmias and sudden cardiac death. | 1-gen-2004 | Priori, SILVIA GIULIANA; Napolitano, C. | |
Nav1.5 E1053K mutation causing Brugada syndrome blocks binding to ankyrin-G and expression of Nav1.5 on the surface of cardiomyocytes. | 1-gen-2004 | Mohler, P. J.; Rivolta, I.; Napolitano, C.; Lemaillet, G.; Lambert, S.; Priori, SILVIA GIULIANA; Bennett, V. |
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