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Mostrati risultati da 61 a 80 di 145
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Long QT syndrome: from genetic basis to treatment 1-gen-2011 Crotti, Lia; Dagradi, F.; Schwartz, Peter
Inherited cardiac arrhythmia syndrome. Role of potassium channels 1-gen-2011 Crotti, Lia; Insolia, Roberto; Schwartz, Peter
Pleiotropic mutations in ion channels: what lies behind them? 1-gen-2011 Crotti, Lia
Inherited cardiac arrhythmia syndrome: Role of potassium channels. 1-gen-2011 Crotti, Lia; Insolia, Roberto; Schwartz, Peter
Transient outward current (I(to)) gain-of-function mutations in the KCND3-encoded Kv4.3 potassium channel and Brugada syndrome. 1-gen-2011 Giudicessi, Jr; Ye, D; Tester, Dj; Crotti, Lia; Mugione, A; Nesterenko, Vv; Albertson, Rm; Antzelevitch, C; Schwartz, Peter; Ackerman, Mj
QTc behavior during exercise and genetic testing for the long-QT syndrome. 1-gen-2011 Schwartz, Peter; Crotti, Lia
Genetic predisposition to sudden cardiac death. 1-gen-2011 Crotti, Lia
Gene expression and arrhythmic risk. 1-gen-2012 Crotti, Lia
Arrhythmogenic disorders of genetic origin. Long QT Syndrome: from genetics to management. 1-gen-2012 Schwartz, Peter; Crotti, Lia; Insolia, Roberto
A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na(v)1.5 and K(v)4.3 channel currents. 1-gen-2012 Hu, D.; Barajas Martínez, H.; Medeiros Domingo, A.; Crotti, Lia; Veltmann, C.; Schimpf, R.; Urrutia, J.; Alday, A.; Casis, O.; Pfeiffer, R.; Burashnikov, E.; Caceres, G.; Tester, D. J.; Wolpert, C.; Borggrefe, M.; Schwartz, Peter; Ackerman, M. J.; Antzelevitch, C.
Vagal reflexes following an exercise stress test: a simple clinical tool for gene-specific risk stratification in the long QT syndrome. 1-gen-2012 Crotti, Lia; Spazzolini, C.; Porretta, A. P.; Dagradi, F.; Taravelli, E.; Petracci, B.; Vicentini, A.; Pedrazzini, M.; La Rovere, M. T.; Vanoli, Emilio; Goosen, A.; Heradien, M.; George AL, J. r.; Brink, P. A.; Schwartz, Peter
When genetic screening for your patient with long QT syndrome comes back negative, don't always take a no for a no. 1-gen-2012 Crotti, Lia; Schwartz, Peter
Torsades de Pointes following Acute Myocardial Infarction: Evidence for a Deadly Link with a Common Genetic Variant. 1-gen-2012 Crotti, Lia; Hu, D; Barajas Martinez, H; DE FERRARI, Gaetano; Oliva, A; Insolia, Roberto; Pollevick, Gd; Dagradi, Federica; Guerchicoff, A; Greco, F; Schwartz, Peter; Viskin, S; Antzelevitch, C.
Not all beta-blockers are equal in the management of long QT syndrome types 1 and 2: higher recurrence of events under metoprolol. 1-gen-2012 Chockalingam, P.; Crotti, Lia; Girardengo, G.; Johnson, J. N.; Harris, K. M.; van der Heijden, J. F.; Hauer, R. N.; Beckmann, B. M.; Spazzolini, C.; Rordorf, R.; Rydberg, A.; Clur, S. A.; Fischer, M.; van den Heuvel, F; . Kääb S, .; Blom, N. A.; Ackerman, M. J.; Schwartz, Peter; Wilde, A. A.
Spectrum and prevalence of mutations involving BrS1-12 susceptibility genes in a cohort of unrelated patients referred for Brugada Syndrome genetic testing: implications for genetic testing. 1-gen-2012 Crotti, Lia; Marcou, Ca; Tester, Dj; Castelletti, Silvia; Giudicessi, Jr; Torchio, Margherita; Medeiros Domingo, A; Savastano, Simone; Will, Ml; Dagradi, Federica; Schwartz, Peter; Ackerman, M. J.
A novel disease gene for Brugada syndrome: sarcolemmal membrane-associated protein gene mutations impair intracellular trafficking of hNav1.5. 1-gen-2012 Ishikawa, T.; Sato, A.; Marcou, C. A.; Tester, Dj; Ackerman, M. J.; Crotti, Lia; Schwartz, Peter; On, Yk; Park, J. E.; Nakamura, K.; Hiraoka, M.; Nakazawa, K.; Sakurada, H.; Arimura, T.; Makita, N.; Kimura, A.
Calmodulin mutations associated with recurrent cardiac arrest in infants. 1-gen-2013 Crotti, Lia; Johnson, C. N.; Graf, E.; DE FERRARI, Gaetano; Cuneo, B. F.; Ovadia, M.; Papagiannis, J.; Feldkamp, M. D.; Rathi, S. G.; Kunic, J. D.; Pedrazzini, M.; Wieland, T.; Lichtner, P.; Beckmann, B. M.; Clark, T.; Shaffer, C.; Benson, D. W.; Kääb, S.; Meitinger, T.; Strom, T. M.; Chazin, W. J.; Schwartz, Peter; George AL, J. r.
Refined multiscale entropy analysis of heart period and QT interval variabilities in long QT syndrome type-1 patients2013 35th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) 1-gen-2013 Vlasta, Bari; Jose F., Valencia; Montserrat, Vallverdu; Girardengo, Giulia; Tito, Bassani; Andrea, Marchi; Laura, Calvillo; Pere, Caminal; Sergio, Cerutti; Paul A., Brink; Crotti, Lia; Schwartz, Peter; Alberto, Porta
FGF12 is a candidate Brugada syndrome locus. 1-gen-2013 Hennessey, J. A.; Marcou, C. A.; Wang, C.; Wei, E. Q.; Wang, C.; Tester, D. J.; Torchio, Margherita; Dagradi, Federica; Crotti, Lia; Schwartz, Peter; Ackerman, M. J.; Pitt, G. S.
Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndrome. 1-gen-2013 Duchatelet, S.; Crotti, Lia; Peat, R. A.; Denjoy, I.; Itoh, H; Berthet, M.; Ohno, S.; Fressart, V.; Monti, MARIA CRISTINA; Crocamo, Cristina; Pedrazzini, Matteo; Dagradi, Federica; Vicentini, A.; Klug, D.; Brink, P. A.; Goosen, A.; Swan, H.; Toivonen, L.; Lahtinen, A. M.; Kontula, K.; Shimizu, W.; Horie, M.; George AL, J. r.; Trégouët, D. A.; Guicheney, P.; Schwartz, Peter
Mostrati risultati da 61 a 80 di 145
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