RIVOLTA ILARIA

Ruolo: 
Professore associato
Settore scientifico disciplinare: 
FISIOLOGIA (BIO/09)
Telefono: 
0264488319
0264488239
0264488302
Stanza: 
U08, Piano: P03, Stanza: 3037
Via Cadore, 48 - 20900 MONZA
U8, Piano: III, Stanza: L3.10B
Via Cadore, 48 - 20900 MONZA

Pubblicazioni

  • 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
  • Juang, J., Lu, T., Chen, C., Lin, L., Hwang, J., Lai, L., et al. (2018). Functional studies of a novel copy number deletion in GSTM3 gene associated with increase of ventricular arrhythmia in patients with Brugada syndrome and ICD implantation. EUROPEAN HEART JOURNAL, 39(Supplement 1), 1203-1203. Dettaglio
  • Bonzanni, M., Difrancesco, J., Milanesi, R., Campostrini, G., Castellotti, B., Bucchi, A., et al. (2018). A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability. NEUROBIOLOGY OF DISEASE, 118, 55-63. Dettaglio