CROTTI, LIA

CROTTI, LIA  

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Risultati 1 - 20 di 138 (tempo di esecuzione: 0.029 secondi).
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A comprehensive electrocardiographic, molecular, and echocardiographic study of Brugada syndrome: validation of the 2013 diagnostic criteria. 1-gen-2014 Savastano, S.; Rordorf, R.; Vicentini, A.; Petracci, B.; Taravelli, E.; Castelletti, S.; D'Errico, A.; Torchio, M.; Dossena, C.; Novara, P.; Dagradi, F.; Landolina, M.; Spazzolini, C.; Crotti, Lia; Schwartz, P. J.
A KCNH2 branch point mutation causing aberrant splicing contributes to an explanation of genotype-negative long QT syndrome. 1-gen-2009 Crotti, Lia; Lewandowska, Ma; Schwartz, Peter; Insolia, Roberto; Pedrazzini, M; Bussani, E; Dagradi, F; George AL, Jr; Pagani, F.
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.
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.
AKAP9 is a genetic modifier of congenuital Long-QT Syndrome type 1 In corso di stampa de Villiers, C. P.; van der Merwe, L.; Crotti, Lia; Goosen, A.; George, A. L.; Schwartz, P. J.; Brink, P. A.; Moolman Smook, J. O.; Corfield, V. A.
All LQT3 patients need an ICD. True or false? 1-gen-2009 Schwartz, Peter; Spazzolini, C; Crotti, Lia
Arrhythmogenic calmodulin mutations disrupt intracellular cardiomyocyte Ca2+ regulation by distinct mechanisms. 1-gen-2014 Yin, G.; Hassan, F.; Haroun, A. R.; Murphy, L. L.; Crotti, Lia; Schwartz, P. J.; George, A. L.; Satin, J.
Arrhythmogenic disorders of genetic origin. Long QT Syndrome: from genetics to management. 1-gen-2012 Schwartz, Peter; Crotti, Lia; Insolia, Roberto
Association of toll-like receptor 7 variants with life-threatening COVID-19 disease in males: Findings from a nested case-control study 1-gen-2021 Fallerini, C.; Daga, S.; Mantovani, S.; Benetti, E.; Picchiotti, N.; Francisci, D.; Paciosi, F.; Schiaroli, E.; Baldassarri, M.; Fava, F.; Palmieri, M.; Ludovisi, S.; Castelli, F.; Quiros-Roldan, E.; Vaghi, M.; Rusconi, S.; Siano, M.; Bandini, M.; Spiga, O.; Capitani, K.; Furini, S.; Mari, F.; Renieri, A.; Mondelli, M. U.; Frullanti, E.; Valentino, F.; Doddato, G.; Giliberti, A.; Tita, R.; Amitrano, S.; Bruttini, M.; Croci, S.; Meloni, I.; Mencarelli, M. A.; Rizzo, C. L.; Pinto, A. M.; Sarno, L. D.; Beligni, G.; Tommasi, A.; Iuso, N.; Montagnani, F.; Fabbiani, M.; Rossetti, B.; Zanelli, G.; Bargagli, E.; Bergantini, L.; D'Alessandro, M.; Cameli, P.; Bennett, D.; Anedda, F.; Marcantonio, S.; Scolletta, S.; Franchi, F.; Mazzei, M. A.; Guerrini, S.; Conticini, E.; Cantarini, L.; Frediani, B.; Tacconi, D.; Spertilli, C.; Feri, M.; Donati, A.; Scala, R.; Guidelli, L.; Spargi, G.; Corridi, M.; Nencioni, C.; Croci, L.; Caldarelli, G. P.; Spagnesi, M.; Romani, D.; Piacentini, P.; Desanctis, E.; Cappelli, S.; Canaccini, A.; Verzuri, A.; Anemoli, V.; Ognibene, A.; D'Arminio Monforte, A.; Miraglia, F. G.; Girardis, M.; Venturelli, S.; Busani, S.; Cossarizza, A.; Antinori, A.; Vergori, A.; Emiliozzi, A.; Gabrieli, A.; Riva, A.; Scotton, P. G.; Andretta, F.; Panese, S.; Scaggiante, R.; Gatti, F.; Parisi, S. G.; Baratti, S.; Antoni, M. D.; Monica, M. D.; Piscopo, C.; Capasso, M.; Russo, R.; Andolfo, I.; Iolascon, A.; Fiorentino, G.; Carella, M.; Castori, M.; Merla, G.; Squeo, G. M.; Aucella, F.; Raggi, P.; Marciano, C.; Perna, R.; Bassetti, M.; Biagio, A. D.; Sanguinetti, M.; Masucci, L.; Valente, S.; Mandala, M.; Giorli, A.; Salerni, L.; Zucchi, P.; Parravicini, P.; Menatti, E.; Trotta, T.; Giannattasio, F.; Coiro, G.; Lena, F.; Coviello, D. A.; Mussini, C.; Bosio, G.; Martinelli, E.; Mancarella, S.; Tavecchia, L.; Gori, M.; Crotti, L.; Parati, G.; Gabbi, C.; Zanella, I.; Rizzi, M.; Maggiolo, F.; Ripamonti, D.; Bachetti, T.; Rovere, M. T. L.; Sarzi-Braga, S.; Bussotti, M.; Chiariello, M.; Belli, M. A.; Dei, S.
Autonomic control of heart rate and QT interval variability influences arrhythmic risk in long QT syndrome type 1 1-gen-2015 Porta, Alberto; Girardengo, Giulia; Bari, Vlasta; George, Alfred L; Brink, Paul A; Goosen, Althea; Crotti, Lia; Schwartz, Peter
Brugada and Long QT Syndrome are two different diseases: True or False? 1-gen-1999 Priori, SILVIA GIULIANA; Crotti, Lia
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.
Can a message from the dead save lives? 1-gen-2007 Schwartz, Peter; Crotti, Lia
Cardiac arrhythmias of genetic origin are important contributors to Sudden Infant Death Syndrome. 1-gen-2007 Schwartz, Peter; Crotti, Lia
Cardiac potassium channel dysfunction in sudden infant death syndrome. 1-gen-2008 Rhodes, Te; Abraham, Rl; Welch, Rc; Vanoye, Cg; Crotti, Lia; Arnestad, M; Insolia, Roberto; Pedrazzini, M; Ferrandi, C; Vege, A; Rognum, T; Roden, Dm; Schwartz, Peter; George AL, Jr
Cardiac sodium channel dysfunction in sudden infant death syndrome. 1-gen-2007 Wang, Dw; Desai, Rr; Crotti, Lia; Arnestad, M; Insolia, Roberto; Pedrazzini, M; Ferrandi, C; Vege, A; Rognum, T; Schwartz, Peter; George AL, Jr
Characterization of SEMA3A-encoded semaphorin as a naturally cccurring Kv4.3 protein inhibitor and its contribution to Brugada Syndrome 1-gen-2014 Boczek, N. J.; Ye, D.; Johnson, E. K.; Wang, W.; Crotti, Lia; Tester, D. J.; Dagradi, F.; Mizusawa, Y.; Torchio, M.; Alders, M.; Giudicessi, J. R.; Wilde, A. A.; Schwartz, P. J.; Nerbonne, J. M.; Ackerman, M. J.
Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 families. 1-gen-2000 Priori, SILVIA GIULIANA; Napolitano, C; Gasparini, M; Pappone, C; Della Bella, P; Brignole, M; Giordano, U; Giovannini, T; Menozzi, C; Bloise, R; Crotti, Lia; Terreni, L; Schwartz, Peter
Clinical Aspects of Type 3 Long-QT Syndrome: An International Multicenter Study. 1-gen-2016 Wilde, Aa; Moss, Aj; Kaufman, Es; Shimizu, W; Peterson, Dr; Benhorin, J; Lopes, C; Towbin, Ja; Spazzolini, Carla; Crotti, Lia; Zareba, W; Goldenberg, I; Kanters, Jk; Robinson, Jl; Qi, M; Hofman, N; Tester, Dj; Bezzina, Cr; Alders, M; Aiba, T; Kamakura, S; Miyamoto, Y; Andrews, Ml; Mcnitt, S; Polonsky, B; Schwartz, Peter; Ackerman, Mj
Clinical implications for patients with Long QT Syndrome who experience a cardiac event during infancy 1-gen-2009 Spazzolini, C; Mullally, J; Schwartz, Peter; Moss, Aj; Mcnitt, S; Ouellet, G; Fugate, T; Goldenberg, I; Jons, C; Zareba, W; Robinson, Jl; Ackerman, Mj; Benhorin, J; Crotti, Lia; Kaufman, Es; Locati, Eh; Ming, Q; Napolitano, C; Priori, SILVIA GIULIANA; Towbin, Ja; Vincent, G. M.