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Assegnista di ricerca

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Difrancesco, J., Castellotti, B., Milanesi, R., Ragona, F., Freri, E., Canafoglia, L., et al. (2019). HCN ion channels and accessory proteins in epilepsy: genetic analysis of a large cohort of patients and review of the literature. EPILEPSY RESEARCH, 153, 49-58. Dettaglio
Murano, C., Binda, A., Lucano, D., Micaglio, E., Ciconte, G., Ghiroldi, A., et al. (2019). Two novel SCN5A loss-of-function mutations affect patients with severe arrhytmogenic syndromes. Intervento presentato a: FEPS2019 - Federation of European Physiological Societies (FEPS) and the Italian Physiological Society (SIF), Bologna. Dettaglio
Binda, A., Murano, C., DI FRANCESCO, J., Castellotti, B., Milanesi, R., Ragona, F., et al. (2019). Progressive epileptic encephalopathy associated with a novel HCN2 mutation. Intervento presentato a: FEPS 2019 Joint Meeting of the Federation of European Physiological Societies and the Italian Physiological Society, Bologna. Dettaglio
Binda, A., Renna, L., Bosè, F., Brigonzi, E., Botta, A., Valaperta, R., et al. (2018). SCN4A as modifier gene in patients with myotonic dystrophy type 2. SCIENTIFIC REPORTS, 8(1). Dettaglio
Marini, C., Porro, A., Rastetter, A., Dalle, C., Rivolta, I., Bauer, D., et al. (2018). HCN1 mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyond. BRAIN, 141(11), 3160-3178. Dettaglio

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