RIVOLTA ILARIA

Ruolo:

Professore associato

Settore scientifico disciplinare:

FISIOLOGIA (BIO/09)

Afferenza:

E-mail:

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

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

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