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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.
Genetics of cardiac arrhythmias and sudden cardiac death. 1-gen-2004 Priori, SILVIA GIULIANA; Napolitano, C.
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.
Genetics of Cardiac Arrhythmias 1-gen-2004 Priori, SILVIA GIULIANA; Napolitano, C; Schwartz, Peter
Policy statement: ESC-ERC recommendations for the use of automated external defibrillators (AEDs) in Europe. 1-gen-2004 Priori, SILVIA GIULIANA; Bossaert, Ll; Chamberlain, Da; Napolitano, C; Arntz, Hr; Koster, Rw; Monsieurs, Kg; Capucci, A; Wellens, Hh
Association of long QT syndrome loci and cardiac events among patients treated with beta-blockers 1-gen-2004 Priori, SILVIA GIULIANA; Napolitano, C.; Schwartz, Peter; Grillo, M.; Bloise, R.; Ronchetti, E; . Moncalvo C, .; Tulipani, C.; Veia, A.; Bottelli, G.; Nastoli, J.
Abnormal Calcium Signalling and Sudden Cardiac Death Associated With Mutation of Calsequestrin. 1-gen-2004 Viatchenko Karpinski, S; Terentyev, D; Gyorke, I; Terentyeva, R; Volpe, P; Priori, SILVIA GIULIANA; Napolitano, C; Nori, A; Williams, Sc; Gyorke, S.
A cardiac arrhythmia syndrome caused by loss of ankyrin-B function 1-gen-2004 Mohler, P.; Splawski, I.; Napolitano, C.; Bottelli, G.; Sharpe, L.; Timothy, K.; Priori, SILVIA GIULIANA; Keating, M.; Bennett, V.
Loss of function associated with novel mutations of the SCN5A gene in patients with Brugada syndrome 1-gen-2004 Baroudi, G; Napolitano, C; Priori, SILVIA GIULIANA; Del Bufalo, A; Chahine, M.
Experimental Therapy of genetic arrhythmias: disease-specific pharmacology. 1-gen-2005 Priori, SILVIA GIULIANA; Napolitano, C; Cerrone, M.
Cardiac and skeletal muscle disorders caused by mutations in the intracellular Ca release channels 1-gen-2005 Priori, SILVIA GIULIANA; Napolitano, C.
Cardiac Histological Substrate in Patients With Clinical Phenotype of Brugada Syndrome 1-gen-2005 Frustaci, A.; Priori, SILVIA GIULIANA; Pieroni, M.; Chimenti, C.; Napolitano, C.; Rivolta, I.; Sanna, T.; Bellocci, F.; Russo, M. A.
Intracellular calcium handling dysfunction and arrhythmogenesis: a new challenge for the electrophysiologist 1-gen-2005 Priori, SILVIA GIULIANA; Napolitano, Carlo
Should patients with an asymptomatic Brugada electrocardiogram undergo pharmacological and electrophysiological testing? 1-gen-2005 Priori, SILVIA GIULIANA; Napolitano, C.
Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice 1-gen-2005 Napolitano, C.; Priori, SILVIA GIULIANA; Schwartz, Peter; Bloise, R.; Ronchetti, E.; Nastoli, J.; Bottelli, G.; Cerrone, Marina; Leonardi, S.
Bidirectional Ventricular Tachycardia and Fibrillation Elicited in a Knock-In Mouse Model Carrier of a Mutation in the Cardiac Ryanodine Receptor (RyR2) 1-gen-2005 Cerrone, Marina; Colombi, Barbara; Santoro, M; RAFFAELE DI BARLETTA, M; Scelsi, M; Villani, L; Napolitano, C; Priori, SILVIA GIULIANA
A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene. 1-gen-2005 Priori, SILVIA GIULIANA; Pandit, Sv; Rivolta, I; Berenfeld, O; Ronchetti, E; Dhamoon, A; Napolitano, C; Anumonwo, J; Raffaele Di Barletta, M; Gudapakkam, S; Bosi, G; Stramba Badiale, M; Jalife, J.
TRANSGENIC ANIMAL MODEL FOR CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA (CPVT) AND USE THEREFORE 1-gen-2006 Priori, SILVIA GIULIANA; Napolitano, C.
Risk of aborted cardiac arrest or sudden cardiac death during adolescence in the long-QT syndrome. 1-gen-2006 Hobbs, Jb; Peterson, Dr; Moss, Aj; Mcnitt, S; Zareba, W; Goldenberg, I; Qi, M; Robinson, Jl; Sauer, Aj; Ackerman, Mj; Benhorin, J; Kaufman, Es; Locati, Eh; Napolitano, C; Priori, SILVIA GIULIANA; Towbin, Ja; Vincent, Gm; Zhang, L.
Female predominance and transmission distortion in the long-QT syndrome 1-gen-2006 Imboden, M; Swan, H; Denjoy, I; Van Langen, Im; Latinen Forsblom, Pj; Napolitano, C; Fressart, V; Breithardt, G; Berthet, M; Priori, SILVIA GIULIANA; Hainque, B; Wilde, Aa; Schulze Bahr, E; Feingold, J; Guicheney, P.
Mostrati risultati da 81 a 100 di 241
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