CASTELLETTI, SILVIA
CASTELLETTI, SILVIA
Desmoplakin missense and non-missense mutations in arrhythmogenic right ventricular cardiomyopathy: Genotype-phenotype correlation.
2017-01-01 Castelletti, Silvia; Vischer, As; Syrris, P; Crotti, Lia; Spazzolini, Carla; Ghidoni, Alice; Parati, G; Jenkins, S; Kotta, Mc; Mckenna, Wj; Schwartz, Peter; Pantazis, A.
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.
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi003-A from a patient affected by an autosomal recessive form of Long QT Syndrome type 1
2018-01-01 Mura, Manuela; Ginevrino, Monia; Zappatore, Rita; Pisano, Federica; Boni, Marina; Castelletti, Silvia; Crotti, Lia; Valente, Enza Maria; Schwartz, Peter J; Gnecchi, Massimiliano
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.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Desmoplakin missense and non-missense mutations in arrhythmogenic right ventricular cardiomyopathy: Genotype-phenotype correlation. | 1-gen-2017 | Castelletti, Silvia; Vischer, As; Syrris, P; Crotti, Lia; Spazzolini, Carla; Ghidoni, Alice; Parati, G; Jenkins, S; Kotta, Mc; Mckenna, Wj; Schwartz, Peter; Pantazis, A. | |
| 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. | |
| Generation of the human induced pluripotent stem cell (hiPSC) line PSMi003-A from a patient affected by an autosomal recessive form of Long QT Syndrome type 1 | 1-gen-2018 | Mura, Manuela; Ginevrino, Monia; Zappatore, Rita; Pisano, Federica; Boni, Marina; Castelletti, Silvia; Crotti, Lia; Valente, Enza Maria; Schwartz, Peter J; Gnecchi, Massimiliano | |
| 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. |