PEDRAZZINI, MATTEO
PEDRAZZINI, MATTEO
DIPARTIMENTO DI MEDICINA MOLECOLARE
Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndrome.
2013-01-01 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
KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome.
2005-01-01 Crotti, Lia; Lundquist, Al; Insolia, Roberto; Pedrazzini, Matteo; Ferrandi, Chiara; DE FERRARI, Gaetano; Vicentini, Alessandro; Yang, P; Roden, Dm; George AL, Jr; Schwartz, Peter
MTMR4 SNVs modulate ion channel degradation and clinical severity in congenital long QT syndrome: insights in the mechanism of action of protective modifier genes
2020-01-01 Lee, Yee-Ki; Sala, Luca; Mura, Manuela; Rocchetti, Marcella; Pedrazzini, Matteo; Ran, Xinru; Mak, Timothy S H; Crotti, Lia; Sham, Pak C; Torre, Eleonora; Zaza, Antonio; Schwartz, Peter J; Tse, Hung-Fat; Gnecchi, Massimiliano
The genetics underlying acquired long QT syndrome: impact for genetic screening.
2016-01-01 Itoh, H; Crotti, Lia; Aiba, T; Spazzolini, Carla; Denjoy, I; Fressart, V; Hayashi, K; Nakajima, T; Ohno, S; Makiyama, T; Wu, J; Hasegawa, K; Mastantuono, E; Dagradi, Federica; Pedrazzini, Matteo; Yamagishi, M; Berthet, M; Murakami, Y; Shimizu, W; Guicheney, P; Schwartz, Peter; Horie, M.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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 | |
| KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome. | 1-gen-2005 | Crotti, Lia; Lundquist, Al; Insolia, Roberto; Pedrazzini, Matteo; Ferrandi, Chiara; DE FERRARI, Gaetano; Vicentini, Alessandro; Yang, P; Roden, Dm; George AL, Jr; Schwartz, Peter | |
| MTMR4 SNVs modulate ion channel degradation and clinical severity in congenital long QT syndrome: insights in the mechanism of action of protective modifier genes | 1-gen-2020 | Lee, Yee-Ki; Sala, Luca; Mura, Manuela; Rocchetti, Marcella; Pedrazzini, Matteo; Ran, Xinru; Mak, Timothy S H; Crotti, Lia; Sham, Pak C; Torre, Eleonora; Zaza, Antonio; Schwartz, Peter J; Tse, Hung-Fat; Gnecchi, Massimiliano | |
| The genetics underlying acquired long QT syndrome: impact for genetic screening. | 1-gen-2016 | Itoh, H; Crotti, Lia; Aiba, T; Spazzolini, Carla; Denjoy, I; Fressart, V; Hayashi, K; Nakajima, T; Ohno, S; Makiyama, T; Wu, J; Hasegawa, K; Mastantuono, E; Dagradi, Federica; Pedrazzini, Matteo; Yamagishi, M; Berthet, M; Murakami, Y; Shimizu, W; Guicheney, P; Schwartz, Peter; Horie, M. |