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Mostrati risultati da 1 a 19 di 19
Titolo Data di pubblicazione Autore(i) File
Molecular Bases of Juvenile Sudden Cardiac Death. 1-gen-1999 Priori, SILVIA GIULIANA; Cerrone, Marina
Ion Channel Diseases and Sudden Cardiac Death 1-gen-1999 Priori, SILVIA GIULIANA; Cerrone, Marina
La Sindrome di Brugada 1-gen-2003 Priori, SILVIA GIULIANA; Cerrone, Marina
La Sindrome di Brugada: aspetti clinici, criteri diagnostici, stratificazione prognostica. 1-gen-2003 Cerrone, Marina; Grillo, M; Priori, SILVIA GIULIANA
Molecular genetics: is it making an impact in the management of inherited arrhythmogenic syndromes? 1-gen-2005 Priori, SILVIA GIULIANA; Cerrone, Marina
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
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.
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.
La Sindrome di Brugada 1-gen-2009 Priori, SILVIA GIULIANA; Cerrone, Marina
Routine electrocardiogram and medical history in syncope: a simple approach can identify most high-risk patients 1-gen-2009 Cerrone, Marina; Priori, SILVIA GIULIANA
Long QT syndrome and catecholaminergic VT 1-gen-2010 Cerrone, Marina; S., Yaghoubian; Priori, SILVIA GIULIANA
Genetics of sudden death: focus on inherited channelopathies 1-gen-2011 Cerrone, Marina; Priori, SILVIA GIULIANA
Genetics of ion-channel disorders 1-gen-2012 Cerrone, Marina; Napolitano, C; Priori, SILVIA GIULIANA
A clinical approach to inherited arrhythmias 1-gen-2012 Cerrone, Marina; Cummings, S; Alansari, T; Priori, SILVIA GIULIANA
KCNJ2 mutation in short QT syndrome 3 results in atrial fibrillation and ventricular proarrhythmia. 1-gen-2013 Deo, M; Ruan, Y; Pandit, Sv; Shah, K; Berenfeld, O; Blaufox, A; Cerrone, Marina; Noujaim, Sf; Denegri, M; Jalife, J; Priori, SILVIA GIULIANA
Genetically engineered SCN5A mutant pig hearts exhibit conduction defects and arrhythmias 1-gen-2015 Park, David S.; Cerrone, Marina; Morley, Gregory; Vasquez, Carolina; Fowler, Steven; Liu, Nian; Bernstein, Scott A.; Liu, Fang Yu; Zhang, Jie; Rogers, Christopher S.; Priori, SILVIA GIULIANA; Chinitz, Larry A.; Fishman, Glenn I.
Implantable Loop Recorder in Inherited Arrhythmia Diseases: A Critical Tool for Symptom Diagnosis and Advanced Risk Stratification 1-gen-2018 Dwivedi, A; Joza, J; Malkani, K; Mendelson, Tb; Priori, Sg; Chinitz, La; Fowler, Sj; Cerrone, M
Management of congenital long-QT syndrome: Commentary from the experts 1-gen-2021 Kaufman, E. S.; Eckhardt, L. L.; Ackerman, M. J.; Aziz, P. F.; Behr, E. R.; Cerrone, M.; Chung, M. K.; Cutler, M. J.; Etheridge, S. P.; Krahn, A. D.; Lubitz, S. A.; Perez, M. V.; Priori, S. G.; Roberts, J. D.; Roden, D. M.; Schulze-Bahr, E.; Schwartz, P. J.; Shimizu, W.; Shoemaker, M. B.; Sy, R. W.; Towbin, J. A.; Viskin, S.; Wilde, A. A. M.; Zareba, W.
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility 1-gen-2022 Barc, J.; Tadros, R.; Glinge, C.; Chiang, D. Y.; Jouni, M.; Simonet, F.; Jurgens, S. J.; Baudic, M.; Nicastro, M.; Potet, F.; Offerhaus, J. A.; Walsh, R.; Choi, S. H.; Verkerk, A. O.; Mizusawa, Y.; Anys, S.; Minois, D.; Arnaud, M.; Duchateau, J.; Wijeyeratne, Y. D.; Muir, A.; Papadakis, M.; Castelletti, S.; Torchio, M.; Ortuno, C. G.; Lacunza, J.; Giachino, D. F.; Cerrato, N.; Martins, R. P.; Campuzano, O.; Van Dooren, S.; Thollet, A.; Kyndt, F.; Mazzanti, A.; Clementy, N.; Bisson, A.; Corveleyn, A.; Stallmeyer, B.; Dittmann, S.; Saenen, J.; Noel, A.; Honarbakhsh, S.; Rudic, B.; Marzak, H.; Rowe, M. K.; Federspiel, C.; Le Page, S.; Placide, L.; Milhem, A.; Barajas-Martinez, H.; Beckmann, B. -M.; Krapels, I. P.; Steinfurt, J.; Winkel, B. G.; Jabbari, R.; Shoemaker, M. B.; Boukens, B. J.; Skoric-Milosavljevic, D.; Bikker, H.; Manevy, F. C.; Lichtner, P.; Ribases, M.; Meitinger, T.; Muller-Nurasyid, M.; Veldink, J. H.; van den Berg, L. H.; Van Damme, P.; Cusi, D.; Lanzani, C.; Rigade, S.; Charpentier, E.; Baron, E.; Bonnaud, S.; Lecointe, S.; Donnart, A.; Le Marec, H.; Chatel, S.; Karakachoff, M.; Bezieau, S.; London, B.; Tfelt-Hansen, J.; Roden, D.; Odening, K. E.; Cerrone, M.; Chinitz, L. A.; Volders, P. G.; van de Berg, M. P.; Laurent, G.; Faivre, L.; Antzelevitch, C.; Kaab, S.; Arnaout, A. A.; Dupuis, J. -M.; Pasquie, J. -L.; Billon, O.; Roberts, J. D.; Jesel, L.; Borggrefe, M.; Lambiase, P. D.; Mansourati, J.; Loeys, B.; Leenhardt, A.; Guicheney, P.; Maury, P.; Schulze-Bahr, E.; Robyns, T.; Breckpot, J.; Babuty, D.; Priori, S. G.; Napolitano, C.; de Asmundis, C.; Brugada, P.; Brugada, R.; Arbelo, E.; Brugada, J.; Mabo, P.; Behar, N.; Giustetto, C.; Molina, M. S.; Gimeno, J. R.; Hasdemir, C.; Schwartz, P. J.; Crotti, L.; Mckeown, P. P.; Sharma, S.; Behr, E. R.; Haissaguerre, M.; Sacher, F.; Rooryck, C.; Tan, H. L.; Remme, C. A.; Postema, P. G.; Delmar, M.; Ellinor, P. T.; Lubitz, S. A.; Gourraud, J. -B.; Tanck, M. W.; George, A. L.; Macrae, C. A.; Burridge, P. W.; Dina, C.; Probst, V.; Wilde, A. A.; Schott, J. -J.; Redon, R.; Bezzina, C. R.
Mostrati risultati da 1 a 19 di 19
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