IRIS

NAPOLITANO, CARLO

NAPOLITANO, CARLO  

DIPARTIMENTO DI MEDICINA MOLECOLARE  

Mostra records
Risultati 1 - 20 di 248 (tempo di esecuzione: 0.042 secondi).
Titolo Data di pubblicazione Autore(i) File
[Computerized tomography study of 32 patients with disk hernia confirmed during surgical intervention]. 1-gen-1986 Bozzao, L.; Amato, F.; Bastianello, Stefano; Cesaris, C. D.; Fantozzi, L. M.; Giannini, A.; Innamorato, A.; Napolitano, C.; Peluso, F.; Petracca, D.
[Role of standard resting ECG in the assessment of sudden cardiac death risk] 1-gen-2014 Napolitano, Carlo; Priori, SILVIA GIULIANA
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.
A method of gene transfer for the treatment of recessive CPVT In corso di stampa Priori, SILVIA GIULIANA; Napolitano, C; Denegri, M.
A molecular basis for the therapy of the long QT syndrome 1-gen-1996 Priori, SILVIA GIULIANA; Napolitano, C; Schwartz, Peter
A Molecular Link between the Sudden Infant Death Syndrome and the Long-QT Syndrome. 1-gen-2000 Schwartz, Peter; Priori, SILVIA GIULIANA; Dumaine, R; Napolitano, C; Antzelevitch, C; Stramba Badiale, M; Richard, Ta; Berti, Mr; Bloise, Raffaella
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.
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.
A Recessive Variant of the Romano-Ward Long QT Syndrome 1-gen-1998 Priori, SILVIA GIULIANA; Schwartz, Peter; Napolitano, C; Bianchi, L; Dennis, A; De Fusco, M; Brown, Am; Casari, G.
A Rule-Free Approach for Cardiological Registry Filling from Italian Clinical Notes with Question Answering Transformers 1-gen-2023 Buonocore, TOMMASO MARIO; Parimbelli, Enea; Tibollo, Valentina; Napolitano, Carlo; Priori, Silvia; Bellazzi, Riccardo
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.
Abnormal Interactions of Calsequestrin With the Ryanodine Receptor Calcium Release Channel Complex Linked to Exercise-Induced Sudden Cardiac Death 1-gen-2006 Terentyev, D; Nori, A; Santoro, M; Viatchenko Karpinski, S; Kubalova, Z; Gyorke, I; Terentyeva, R; Vedamoorthyrao, S; Blom, Na; Valle, G; Napolitano, C; Williams, Sc; Volpe, P; Priori, SILVIA GIULIANA; Gyorke, S.
Abnormal Propagation of Calcium Waves and Ultrastructural Remodeling in Recessive Catecholaminergic Polymorphic Ventricular Tachycardia. 1-gen-2013 Liu, N; Denegri, M; Dun, W; Boncompagni, S; Lodola, F; Protasi, F; Napolitano, C; Boyden, P; Priori, SILVIA GIULIANA
Adeno-associated virus-mediated CASQ2 delivery rescues phenotypic alterations in a patient-specific model of recessive catecholaminergic polymorphic ventricular tachycardia 1-gen-2016 Lodola, F; Morone, D; Denegri, M; Bongianino, R; Nakahama, H; Rutigliano, L; Gosetti, R; Rizzo, G; Vollero, A; Buonocore, M; Napolitano, C; Condorelli, G; Priori, SILVIA GIULIANA; Di Pasquale, E; 3, .
Age and sex-related differences in the clinical manifestations of congenital long QT syndrome: findings from the International Prospective LQTS Registry 1-gen-1998 Locati, Eh; Zareba, W; Moss, Aj; Schwartz, Peter; Vincent, Gm; Lehmann, Mh; Towbin, Ja; Priori, SILVIA GIULIANA; Napolitano, C; Robinson, Jl; Andrews, M; Timothy, K; Hall, Wj
Age of First Arrhythmic Event in Brugada Syndrome: Data From the SABRUS (Survey on Arrhythmic Events in Brugada Syndrome) in 678 Patients 1-gen-2017 Milman, A; Andorin, A; Gourraud, Jb; Sacher, F; Mabo, P; Kim, Sh; Maeda, S; Takahashi, Y; Kamakura, T; Aiba, T; Conte, G; Juang, Jjm; Leshem, E; Rahkovich, M; Hochstadt, A; Mizusawa, Y; Postema, Pg; Arbelo, E; Huang, Z; Denjoy, I; Giustetto, C; Wijeyeratne, Yd; Napolitano, C; Michowitz, Y; Brugada, R; Casado-Arroyo, R; Champagne, J; Calo, L; Sarquella-Brugada, G; Tfelt-Hansen, J; Priori, Sg; Takagi, M; Veltmann, C; Delise, P; Corrado, D; Behr, Er; Gaita, F; Yan, Gx; Brugada, J; Leenhardt, A; Wilde, Aam; Brugada, P; Kusano, Kf; Hirao, K; Nam, Gb; Probst, V; Belhassen, B
Allele-Specific Silencing of Mutant mRNA Rescues Ultrastructural and Arrhythmic Phenotype in Mice Carriers of the R4496C Mutation in the Ryanodine Receptor Gene (RYR2). 1-gen-2017 Bongianino, R; Denegri, M; Mazzanti, Andrea; Lodola, F; Vollero, A.; Boncompagni, S; Fasciano, S; Rizzo, G; Mangione, D; Barbaro, S; Fonso Di, A; Napolitano, C; Auricchio, A; Protasi, F; Priori, SILVIA GIULIANA
Arrhythmogenesis in Catecholaminergic Polymorphic Ventricular Tachycardia: insights from a RyR2 R4496C knock-in mouse model 1-gen-2006 Liu, N; Colombi, B; Memmi, M; Zissimopoulos, S; Rizzi, N; Negri, S; Imbriani, Marcello; Napolitano, C; Lai, Fa; Priori, SILVIA GIULIANA
Arrhythmogenic mechanisms in a mouse model of Catecholaminergic Polymorphic Ventricular Tachycardia. 1-gen-2007 Cerrone, Marina; Noujaim, Sf; Tolkacheva, Eg; Talkachou, A; O'Connell, R; Berenfeld, O; Anumonwo, J; Pandit, Sv; Vikstrom, K; Napolitano, C; Priori, SILVIA GIULIANA; Jalife, J.
Arrhythmogenic Right Ventricular Cardiomyopathy: Clinical Course and Predictors of Arrhythmic Risk 1-gen-2016 Mazzanti, A; Ng, K; Faragli, A; Maragna, R; Chiodaroli, E; Orphanou, N; Monteforte, N; Memmi, M; Gambelli, P; Novelli, V; Bloise, R; Catalano, O; Moro, G; Tibollo, V; Morini, M; Bellazzi, Riccardo; Napolitano, C; Bagnardi, V; Priori, SILVIA GIULIANA