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Gene-specific differences in the circadian variation of ventricular repolarization in the long QT syndrome: a key to sudden death during sleep? 1-gen-2000 Stramba Badiale, M; Priori, SILVIA GIULIANA; Napolitano, C; Locati, Eh; Vinolas, X; Haverkamp, W; Schulze Bahr, E; Goulene, K; Schwartz, Peter
Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndrome 1-gen-2000 Ficker, E; Thomas, D; Viswanathan, Pc; Dennis, At; Priori, SILVIA GIULIANA; Napolitano, C; Memmi, M; Wible, Ba; Kaufman, Es; Iyengar, S; Schwartz, Peter; Rudy, Y; Brown, A. M.
Brugada Syndrome and Sudden Cardiac Death in Children. 1-gen-2000 Priori, SILVIA GIULIANA; Napolitano, C; Giordano, U; Collisani, G; Memmi, M.
The long QT syndrome 1-gen-2000 Schwartz, Peter; Priori, SILVIA GIULIANA; Napolitano, C.
Electrocardiographic prediction of abnormal genotype in congenital long QT syndrome: experience in 101 related family members 1-gen-2001 Kaufman, Es; Priori, SILVIA GIULIANA; Napolitano, C; Schwartz, Peter; Iyengar, S; Elston, Rc; Schnell, Ah; Gorodeski, Ez; Rammohan, G; Bahhur, No; Connuck, D; Verrilli, L; Rosenbaum, Ds; Brown, A. M.
Novel Arrhythmogenic mechanism revealed by Long-QT Syndrome mutation in the Cardiac NA+ Channel 1-gen-2001 Abriel, H; Cabo, C; Wehrens, Xht; Rivolta, I; Motoike, Hk; Memmi, M; Napolitano, C; Priori, SILVIA GIULIANA; Kass, Rs
Clinical Implications for affected parents and siblings of probands with Long QT Syndrome 1-gen-2001 Kimbrough, J; Moss, Aj; Zareba, W; Robinson, Jl; Hall, Wj; Benhorin, J; Locati, Eh; Medina, A; Napolitano, C; Priori, SILVIA GIULIANA; Schwartz, Peter; Timothy, K; Towbin, Ja; Vincent, Gm; Zhang, L.
Concealed arrhythmogenic syndromes: the hidden substrate of idiopathic ventricular fibrillation? 1-gen-2001 Priori, SILVIA GIULIANA; Napolitano, C; Grillo, M.
Cardiac Ion Channel Diseases: Clinical Impact 1-gen-2001 Priori, SILVIA GIULIANA; Napolitano, C; Memmi, M; Ronchetti, E.
Genetics of Arrhythmogenic Disorders 1-gen-2001 Priori, SILVIA GIULIANA; Napolitano, C.
Inherited brugada and LQT-3 syndrome mutations of a single residue of the cardiac sodium channel confer distinct channel and clinical phenotypes 1-gen-2001 Rivolta, I; Abriel, H; Tateyama, M; Liu, H; Memmi, M; Vardas, P; Napolitano, C; Priori, SILVIA GIULIANA; Kass, Rs
Genotype-Phenotype correlation in the Long QT Syndrome. Gene-specific triggers for life-threatening arrhythmias 1-gen-2001 Schwartz, Peter; Priori, SILVIA GIULIANA; Spazzolini, Carla; Moss, Aj; Vincent, Gm; Napolitano, C; Denjoy, I; Guicheney, P; Breithardt, G; Keating, Mt; Towbin, Ja
Mutations in the Cardiac Ryanodine Receptor Gene (hRyR2) Underlie Catecholaminergic Polymorphic Ventricular Tachycardia 1-gen-2001 Priori, SILVIA GIULIANA; Napolitano, C; Tiso, N; Memmi, M; Vignati, G; Bloise, Raffaella; Sorrentino, V; Danieli, Ga
Romano-Ward and other congenital long QT syndromes 1-gen-2002 Bloise, Raffaella; Napolitano, C; Priori, SILVIA GIULIANA
Programmed Electrical Stimulation in Brugada Syndrome: How reproducible are the results? 1-gen-2002 Gasparini, M; Priori, SILVIA GIULIANA; Mantica, M; Coltorti, F; Napolitano, C; Galimberti, P; Bloise, Raffaella; Ceriotti, C.
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.
La sindrome di Brugada: epidemiologia, stratificazione del rischio e management clinico. 1-gen-2002 Grillo, M; Napolitano, C; Bloise, Raffaella; Priori, SILVIA GIULIANA
The Long QT Syndrome 1-gen-2002 Napolitano, C; Priori, SILVIA GIULIANA
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
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