Sfoglia per Autore
Torsades de Pointes following Acute Myocardial Infarction: Evidence for a Deadly Link with a Common Genetic Variant.
2012-01-01 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.
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.
2012-01-01 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.
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
FGF12 is a candidate Brugada syndrome locus.
2013-01-01 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.
Condizioni cliniche associate ad anomalie dell'intervallo QT: Implicazioni cliniche [Clinical conditions associated with abnormal QT interval: clinical implications].
2013-01-01 Crotti, Lia; Dossena, Cinzia; Mastantuono, E.; Dagradi, Federica; Schwartz, Peter
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
2013-01-01 Bezzina, C. R.; Barc, J.; Mizusawa, Y.; Remme, C. A.; Gourraud, J. B.; Simonet, F.; Verkerk, A. O.; Schwartz, Peter; Crotti, Lia; Dagradi, Federica; Guicheney, P.; Fressart, V.; Leenhardt, A.; Antzelevitch, C.; Bartkowiak, S.; Borggrefe, M.; Schimpf, R.; Schulze Bahr, E.; Zumhagen, S.; Behr, E. R.; Bastiaenen, R.; Tfelt Hansen, J.; Olesen, M. S.; Kääb, S.; Beckmann, B. M.; Weeke, P.; Watanabe, H.; Endo, N.; Minamino, T.; Horie, M.; Ohno, S.; Hasegawa, K.; Makita, N.; Nogami, A.; Shimizu, W.; Aiba, T.; Froguel, P.; Balkau, B.; Lantieri, O.; Torchio, Margherita; Wiese, C.; Weber, D.; Wolswinkel, R.; Coronel, R.; Boukens, B. J.; Bézieau, S.; Charpentier, E.; Chatel, S.; Despres, A.; Gros, F.; Kyndt, F.; Lecointe, S.; Lindenbaum, P.; Portero, V.; Violleau, J.; Gessler, M.; Tan, H. L.; Roden, D. M.; Christoffels, V. M.; Le Marec, H.; Wilde, A. A.; Probst, V.; Schott, J. J.; Dina, C.; Redon, R.
Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study
2015-01-01 Behr, Elijah R; Savio Galimberti, Eleonora; Barc, Julien; Holst, Anders G; Petropoulou, Evmorfia; Prins, Bram P; Jabbari, Javad; Torchio, Margherita; Berthet, Myriam; Mizusawa, Yuka; Yang, Tao; Nannenberg, Eline A; Dagradi, Federica; Weeke, Peter; Bastiaenan, Rachel; Ackerman, Michael J; Haunso, Stig; Leenhardt, Antoine; Kääb, Stefan; Probst, Vincent; Redon, Richard; Sharma, Sanjay; Wilde, Arthur; Tfelt Hansen, Jacob; Schwartz, Peter; Roden, Dan M; Bezzina, Connie R; Olesen, Morten; Darbar, Dawood; Guicheney, Pascale; Crotti, Lia; Jamshidi, Yalda
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.
Impact of clinical and genetic findings on the management of young patients with Brugada syndrome.
2016-01-01 Andorin, A; Behr, Er; Denjoy, I; Crotti, Lia; Dagradi, Federica; Jesel, L; Sacher, F; Petit, B; Mabo, P; Maltret, A; Wong, Lc; Degand, B; Bertaux, G; Maury, P; Dulac, Y; Delasalle, B; Gourraud, Jb; Babuty, D; Blom, Na; Schwartz, Peter; Wilde, Aa; Probst, V.
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi002-A from a patient affected by the Jervell and Lange-Nielsen syndrome and carrier of two compound heterozygous mutations on the KCNQ1 gene
2018-01-01 Mura, Manuela; Lee, Yee-Ki; Ginevrino, Monia; Zappatore, Rita; Pisano, Federica; Boni, Marina; Dagradi, Federica; Crotti, Lia; Valente, Enza Maria; Schwartz, Peter J; Tse, Hung-Fat; Gnecchi, Massimiliano
From patient-specific induced pluripotent stem cells to clinical translation in long QT syndrome Type 2
2019-01-01 Schwartz, P. J.; Gnecchi, M.; Dagradi, F.; Castelletti, S.; Parati, G.; Spazzolini, C.; Sala, L.; Crotti, L.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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. | |
| 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. | |
| 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 | |
| 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. | |
| Condizioni cliniche associate ad anomalie dell'intervallo QT: Implicazioni cliniche [Clinical conditions associated with abnormal QT interval: clinical implications]. | 1-gen-2013 | Crotti, Lia; Dossena, Cinzia; Mastantuono, E.; Dagradi, Federica; Schwartz, Peter | |
| Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death. | 1-gen-2013 | Bezzina, C. R.; Barc, J.; Mizusawa, Y.; Remme, C. A.; Gourraud, J. B.; Simonet, F.; Verkerk, A. O.; Schwartz, Peter; Crotti, Lia; Dagradi, Federica; Guicheney, P.; Fressart, V.; Leenhardt, A.; Antzelevitch, C.; Bartkowiak, S.; Borggrefe, M.; Schimpf, R.; Schulze Bahr, E.; Zumhagen, S.; Behr, E. R.; Bastiaenen, R.; Tfelt Hansen, J.; Olesen, M. S.; Kääb, S.; Beckmann, B. M.; Weeke, P.; Watanabe, H.; Endo, N.; Minamino, T.; Horie, M.; Ohno, S.; Hasegawa, K.; Makita, N.; Nogami, A.; Shimizu, W.; Aiba, T.; Froguel, P.; Balkau, B.; Lantieri, O.; Torchio, Margherita; Wiese, C.; Weber, D.; Wolswinkel, R.; Coronel, R.; Boukens, B. J.; Bézieau, S.; Charpentier, E.; Chatel, S.; Despres, A.; Gros, F.; Kyndt, F.; Lecointe, S.; Lindenbaum, P.; Portero, V.; Violleau, J.; Gessler, M.; Tan, H. L.; Roden, D. M.; Christoffels, V. M.; Le Marec, H.; Wilde, A. A.; Probst, V.; Schott, J. J.; Dina, C.; Redon, R. | |
| Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study | 1-gen-2015 | Behr, Elijah R; Savio Galimberti, Eleonora; Barc, Julien; Holst, Anders G; Petropoulou, Evmorfia; Prins, Bram P; Jabbari, Javad; Torchio, Margherita; Berthet, Myriam; Mizusawa, Yuka; Yang, Tao; Nannenberg, Eline A; Dagradi, Federica; Weeke, Peter; Bastiaenan, Rachel; Ackerman, Michael J; Haunso, Stig; Leenhardt, Antoine; Kääb, Stefan; Probst, Vincent; Redon, Richard; Sharma, Sanjay; Wilde, Arthur; Tfelt Hansen, Jacob; Schwartz, Peter; Roden, Dan M; Bezzina, Connie R; Olesen, Morten; Darbar, Dawood; Guicheney, Pascale; Crotti, Lia; Jamshidi, Yalda | |
| 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. | |
| Impact of clinical and genetic findings on the management of young patients with Brugada syndrome. | 1-gen-2016 | Andorin, A; Behr, Er; Denjoy, I; Crotti, Lia; Dagradi, Federica; Jesel, L; Sacher, F; Petit, B; Mabo, P; Maltret, A; Wong, Lc; Degand, B; Bertaux, G; Maury, P; Dulac, Y; Delasalle, B; Gourraud, Jb; Babuty, D; Blom, Na; Schwartz, Peter; Wilde, Aa; Probst, V. | |
| Generation of the human induced pluripotent stem cell (hiPSC) line PSMi002-A from a patient affected by the Jervell and Lange-Nielsen syndrome and carrier of two compound heterozygous mutations on the KCNQ1 gene | 1-gen-2018 | Mura, Manuela; Lee, Yee-Ki; Ginevrino, Monia; Zappatore, Rita; Pisano, Federica; Boni, Marina; Dagradi, Federica; Crotti, Lia; Valente, Enza Maria; Schwartz, Peter J; Tse, Hung-Fat; Gnecchi, Massimiliano | |
| From patient-specific induced pluripotent stem cells to clinical translation in long QT syndrome Type 2 | 1-gen-2019 | Schwartz, P. J.; Gnecchi, M.; Dagradi, F.; Castelletti, S.; Parati, G.; Spazzolini, C.; Sala, L.; Crotti, L. |
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