Professore associato
Settore scientifico disciplinare: 
U08, Piano: P03, Stanza: 3037
Via Cadore, 48 - 20900 MONZA
U8, Piano: III, Stanza: L3.10B
Via Cadore, 48 - 20900 MONZA


  • Porro, A., Binda, A., Pisoni, M., Donadoni, C., Rivolta, I., & Saponaro, A. (2020). Rational design of a mutation to investigate the role of the brain protein TRIP8b in limiting the cAMP response of HCN channels in neurons. JOURNAL OF GENERAL PHYSIOLOGY, 152(9). Dettaglio
  • 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. Dettaglio
  • Rivolta, I., Binda, A., Masi, A., & DiFrancesco, J. (2020). Cardiac and neuronal HCN channelopathies. PFLÜGERS ARCHIV. 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
  • 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). Dettaglio