PERCETTI, MARCO
PERCETTI, MARCO
The clinical spectrum of ANO3-Report of a new family and literature review
2024 M. Percetti, M. Zini, P. Soliveri, F. Cogiamanian, M. Ferrara, E. Orunesu, A. Ranghetti, C. Ferrarese, G. Pezzoli, B. Garavaglia, I.U. Isaias, G. Sacilotto
Reply to: Lack of Association between TWNK Rare Variants and Parkinson's Disease in a Chinese Cohort
2023 M. Percetti, E. Monfrini, L. Caporali, R. Minardi, V. Carelli, E.M. Valente, A. Di Fonzo
Harmonizing Genetic Testing for Parkinson's Disease: Results of the PARKNET Multicentric Study
2023 A. Di Fonzo, M. Percetti, E. Monfrini, I. Palmieri, A. Albanese, M. Avenali, A. Bartoletti-Stella, F. Blandini, G. Brescia, G. Calandra-Buonaura, R. Campopiano, S. Capellari, I. Colangelo, G.P. Comi, G. Cuconato, R. Ferese, C. Galandra, S. Gambardella, B. Garavaglia, A. Gaudio, E. Giardina, F. Invernizzi, P. Mandich, R. Mineri, C. Panteghini, C. Reale, L. Trevisan, S. Zampatti, P. Cortelli, E.M. Valente
TWNK in Parkinson's Disease: A Movement Disorder and Mitochondrial Disease Center Perspective Study
2022 M. Percetti, G. Franco, E. Monfrini, L. Caporali, R. Minardi, C. La Morgia, M.L. Valentino, R. Liguori, I. Palmieri, D. Ottaviani, M. Vizziello, D. Ronchi, F. Di Berardino, A. Cocco, B. Macao, M. Falkenberg, G.P. Comi, A. Albanese, B. Giometto, E.M. Valente, V. Carelli, A. Di Fonzo
VPS13C-associated Parkinson's disease : Two novel cases and review of the literature
2022 E. Monfrini, F. Spagnolo, M. Canesi, A. Seresini, B. Passarella, M. Percetti, M. Seia, S. Goldwurm, V. Cereda, G.P. Comi, G. Pezzoli, A. Di Fonzo
Reply to: No association between rare TWNK variants and Parkinson's disease in European cohorts
2022 M. Percetti, E. Monfrini, L. Caporali, R. Minardi, V. Carelli, E.M. Valente, A. Di Fonzo
Screening of LRP10 mutations in Parkinson's disease patients from Italy
2021 A. Manini, L. Straniero, E. Monfrini, M. Percetti, M. Vizziello, G. Franco, V. Rimoldi, A. Zecchinelli, G. Pezzoli, S. Corti, G.P. Comi, S. Duga, A. Di Fonzo
Childhood-onset dystonia with cerebellar signs: expanding the spectrum of GNAL mutations
2020 R. Erro, A. Di Fonzo, M. Percetti, E. Monfrini, S. Scannapieco, M. Picillo, P. Barone