BINDA ANNA

Ruolo:

Assegnista di ricerca

Settore scientifico disciplinare:

FISIOLOGIA (BIO/09)

Afferenza:

E-mail:

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
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, Italy. Dettaglio
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
Binda, A., Panariti, A., Barbuti, A., Murano, C., Dal Magro, R., Masserini, M., et al. (2018). Modulation of the intrinsic neuronal excitability by multifunctional liposomes tailored for treatment of Alzheimer’s disease. INTERNATIONAL JOURNAL OF NANOMEDICINE, 2018/13, 4059-4071. 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

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