RIVOLTA ILARIA

Room: 
U08, Piano: P03, Stanza: 3037
Via Cadore 48 - 20900 MONZA
U8, Piano: III, Stanza: L3.10B
Via Cadore 48 - 20900 MONZA
Role: 
Associate professor
Academic disciplines: 
PHYSIOLOGY (BIO/09)
Telephone: 
0264488319
0264488239
0264488302

Publications

  • Rivolta, I., Binda, A., Masi, A., & DiFrancesco, J. (2020). Cardiac and neuronal HCN channelopathies. PFLÜGERS ARCHIV.
  • Juang, J., Binda, A., Lee, S., Hwang, J., Chen, W., Liu, Y., et al. (2020). GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death. EBIOMEDICINE, 57, 102843.
  • 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.
  • 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.
  • 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. In Special Issue: Joint Meeting of the Federation of European Physiological Societies (FEPS) and the Italian Physiological Society (SIF) Bologna (Italy), September 10th – 13th 2019 (pp.22).