BINDA ANNA

Pubblicazioni

  • 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