Sfoglia per Autore
Cardiac sodium channel dysfunction in sudden infant death syndrome.
2007-01-01 Wang, Dw; Desai, Rr; Crotti, Lia; Arnestad, M; Insolia, Roberto; Pedrazzini, M; Ferrandi, C; Vege, A; Rognum, T; Schwartz, Peter; George AL, Jr
Electrocardiographic and genetic screening for long QT syndrome: results from a prospective study on 44,596 neonates.
2007-01-01 Schwartz, Peter; Stramba Badiale, M; Crotti, Lia; Goulene, K; Pedrazzini, M; Mannarino, S; Salice, P; Bosi, G; Nespoli, L; Rimini, A; Gabbarini, F; Rosati, E; Schwartz, Pj
Gene symbol: SCN5A
2007-01-01 Crotti, Lia; Ferrandi, C; Insolia, R; Pedrazzini, M; Andreoli, E; Veia, A; Crimi, G; Agnetti, A; DE FERRARI, Gaetano; Schwartz, Peter
Gene symbol: SCN5A
2007-01-01 Crotti, Lia; Ferrandi, C; Insolia, R; Pedrazzini, M; Tosin, L; Veia, A; Turco, A; De Ferrari, Gm; Schwartz, Peter
Gene symbol: KCNH2
2007-01-01 Crotti, Lia; Insolia, R; Pedrazzini, M; Andreoli, E; Gabanti, E; Moncalvo, C; Crimi, G; DE FERRARI, Gaetano; Schwartz, Peter
Gene symbol: KCNH2
2007-01-01 Crotti, Lia; Pedrazzini, M.; Ferrandi, C.; Insolia, Roberto; Tosin, L.; Vicentini, A.; Turco, A.; DE FERRARI, Gaetano; Schwartz, P. J.
Gene symbol: KCNQ1
2007-01-01 Crotti, Lia; Insolia, R; Pedrazzini, M; Ferrandi, C; Tosin, L; Moncalvo, C; Turco, A; Agnetti, A; DE FERRARI, Gaetano; Schwartz, P. j.
Functional characterization and molecular correction of the LQT2 KCNH2-Q376 splicing mutation. Therapeutic implications?
2008-01-01 Crotti, Lia; Lewandowska, M; Pedrazzini, M; Insolia, R; Ferrandi, C; Cuoretti, A; Bussani, E; Pagani, F; Schwartz, Peter
Gene symbol: KCNQ1.
2008-01-01 Crotti, Lia; Ferrandi, C; Pedrazzini, M; Insolia, R; Cuoretti, A; Celano, G; Dagradi, F; Stramba Badiale, M; Schwartz, Peter
The LQT2 KCNH2-Q376Q splicing muation: functional characterization, molecular correction and therapeutic implication.
2008-01-01 Insolia, R; Crotti, Lia; Pedrazzini, M; Lewandowska, Ma; Bussani, E; Cuoretti, A; Ghidoni, A; Schwartz, Peter; Pagani, F.
Gene symbol: SCN5A.
2008-01-01 Crotti, Lia; Pedrazzini, M; Insolia, R; Ferrandi, C; Ghidoni, A; Sanzo, A; Dagradi, F; De Ferrari, Gm; Schwartz, Peter
Gene symbol: KCNQ1.
2008-01-01 Crotti, Lia; Insolia, R; Ferrandi, C; Pedrazzini, M; Cuoretti, A; Gandolfi, E; Sanzo, A; Dagradi, F; Schwartz, Peter
Gene symbol: KCNH2.
2008-01-01 Crotti, Lia; Pedrazzini, M; Insolia, R; Ferrandi, C; Cuoretti, A; Celano, G; Gandolfi, E; Dagradi, F; Schwartz, Peter
Gene symbol: KCNH2.
2008-01-01 Crotti, Lia; Pedrazzini, M; Insolia, R; Ferrandi, C; Cuoretti, A; Gandolfi, E; Celano, G; Dagradi, F; Schwartz, Peter
Gene symbol: KCNH2
2008-01-01 Crotti, Lia; Pedrazzini, M; Ferrandi, C; Insolia, R; Cuoretti, A; Dagradi, F; Crimi, G; Coto, E; Reguero, Jr; Schwartz, Peter
Gene symbol: SCN5A.
2008-01-01 Crotti, Lia; Ferrandi, C; Pedrazzini, M; Insolia, R; Cuoretti, A; Sanzo, A; Dagradi, F; DE FERRARI, Gaetano; Schwartz, Peter
Sudden cardiac death in infancy: Focus on prolonged repolarization
2008-01-01 Schwartz, Peter; Stramba Badiale, M; Crotti, Lia; Ackerman, Mj
The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome.
2008-01-01 Makita, N; Behr, E; Shimizu, W; Horie, M; Sunami, A; Crotti, Lia; Schulze Bahr, E; Fukuhara, S; Mochizuki, N; Makiyama, T; Itoh, H; Christiansen, M; Mckeown, P; Miyamoto, K; Kamakura, S; Tsutsui, H; Schwartz, Peter; George AL, Jr; Roden, Dm
Congenital long QT syndrome.
2008-01-01 Crotti, Lia; Celano, G; Dagradi, F; Schwartz, Peter
Cardiac potassium channel dysfunction in sudden infant death syndrome.
2008-01-01 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
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
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 | |
Electrocardiographic and genetic screening for long QT syndrome: results from a prospective study on 44,596 neonates. | 1-gen-2007 | Schwartz, Peter; Stramba Badiale, M; Crotti, Lia; Goulene, K; Pedrazzini, M; Mannarino, S; Salice, P; Bosi, G; Nespoli, L; Rimini, A; Gabbarini, F; Rosati, E; Schwartz, Pj | |
Gene symbol: SCN5A | 1-gen-2007 | Crotti, Lia; Ferrandi, C; Insolia, R; Pedrazzini, M; Andreoli, E; Veia, A; Crimi, G; Agnetti, A; DE FERRARI, Gaetano; Schwartz, Peter | |
Gene symbol: SCN5A | 1-gen-2007 | Crotti, Lia; Ferrandi, C; Insolia, R; Pedrazzini, M; Tosin, L; Veia, A; Turco, A; De Ferrari, Gm; Schwartz, Peter | |
Gene symbol: KCNH2 | 1-gen-2007 | Crotti, Lia; Insolia, R; Pedrazzini, M; Andreoli, E; Gabanti, E; Moncalvo, C; Crimi, G; DE FERRARI, Gaetano; Schwartz, Peter | |
Gene symbol: KCNH2 | 1-gen-2007 | Crotti, Lia; Pedrazzini, M.; Ferrandi, C.; Insolia, Roberto; Tosin, L.; Vicentini, A.; Turco, A.; DE FERRARI, Gaetano; Schwartz, P. J. | |
Gene symbol: KCNQ1 | 1-gen-2007 | Crotti, Lia; Insolia, R; Pedrazzini, M; Ferrandi, C; Tosin, L; Moncalvo, C; Turco, A; Agnetti, A; DE FERRARI, Gaetano; Schwartz, P. j. | |
Functional characterization and molecular correction of the LQT2 KCNH2-Q376 splicing mutation. Therapeutic implications? | 1-gen-2008 | Crotti, Lia; Lewandowska, M; Pedrazzini, M; Insolia, R; Ferrandi, C; Cuoretti, A; Bussani, E; Pagani, F; Schwartz, Peter | |
Gene symbol: KCNQ1. | 1-gen-2008 | Crotti, Lia; Ferrandi, C; Pedrazzini, M; Insolia, R; Cuoretti, A; Celano, G; Dagradi, F; Stramba Badiale, M; Schwartz, Peter | |
The LQT2 KCNH2-Q376Q splicing muation: functional characterization, molecular correction and therapeutic implication. | 1-gen-2008 | Insolia, R; Crotti, Lia; Pedrazzini, M; Lewandowska, Ma; Bussani, E; Cuoretti, A; Ghidoni, A; Schwartz, Peter; Pagani, F. | |
Gene symbol: SCN5A. | 1-gen-2008 | Crotti, Lia; Pedrazzini, M; Insolia, R; Ferrandi, C; Ghidoni, A; Sanzo, A; Dagradi, F; De Ferrari, Gm; Schwartz, Peter | |
Gene symbol: KCNQ1. | 1-gen-2008 | Crotti, Lia; Insolia, R; Ferrandi, C; Pedrazzini, M; Cuoretti, A; Gandolfi, E; Sanzo, A; Dagradi, F; Schwartz, Peter | |
Gene symbol: KCNH2. | 1-gen-2008 | Crotti, Lia; Pedrazzini, M; Insolia, R; Ferrandi, C; Cuoretti, A; Celano, G; Gandolfi, E; Dagradi, F; Schwartz, Peter | |
Gene symbol: KCNH2. | 1-gen-2008 | Crotti, Lia; Pedrazzini, M; Insolia, R; Ferrandi, C; Cuoretti, A; Gandolfi, E; Celano, G; Dagradi, F; Schwartz, Peter | |
Gene symbol: KCNH2 | 1-gen-2008 | Crotti, Lia; Pedrazzini, M; Ferrandi, C; Insolia, R; Cuoretti, A; Dagradi, F; Crimi, G; Coto, E; Reguero, Jr; Schwartz, Peter | |
Gene symbol: SCN5A. | 1-gen-2008 | Crotti, Lia; Ferrandi, C; Pedrazzini, M; Insolia, R; Cuoretti, A; Sanzo, A; Dagradi, F; DE FERRARI, Gaetano; Schwartz, Peter | |
Sudden cardiac death in infancy: Focus on prolonged repolarization | 1-gen-2008 | Schwartz, Peter; Stramba Badiale, M; Crotti, Lia; Ackerman, Mj | |
The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome. | 1-gen-2008 | Makita, N; Behr, E; Shimizu, W; Horie, M; Sunami, A; Crotti, Lia; Schulze Bahr, E; Fukuhara, S; Mochizuki, N; Makiyama, T; Itoh, H; Christiansen, M; Mckeown, P; Miyamoto, K; Kamakura, S; Tsutsui, H; Schwartz, Peter; George AL, Jr; Roden, Dm | |
Congenital long QT syndrome. | 1-gen-2008 | Crotti, Lia; Celano, G; Dagradi, F; Schwartz, Peter | |
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 |
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