Sfoglia per Autore
Unravelling Genetic Factors Underlying Corticobasal Syndrome: A Systematic Review
2021 F. Arienti, G. Lazzeri, M. Vizziello, E. Monfrini, N. Bresolin, M.C. Saetti, M. Picillo, G. Franco, A. Di Fonzo
Leukoencephalopathy with calcifications and cysts: Genetic and phenotypic spectrum
2021 Y.J. Crow, H. Marshall, G.I. Rice, L. Seabra, E.M. Jenkinson, K. Baranano, R. Battini, A. Berger, E. Blair, T. Blauwblomme, F. Bolduc, N. Boddaert, J. Buckard, H. Burnett, S. Calvert, R. Caumes, A.C.-. Ng, D. Chiang, D.B. Clifford, D.M. Cordelli, A. de Burca, N. Demic, I. Desguerre, L. De Waele, A. Di Fonzo, S.R. Dunham, S. Dyack, F. Elmslie, M. Ferrand, G. Fisher, E.G. Karimiani, J. Ghoumid, F. Gibbon, H. Goel, H.T. Hilmarsen, I. Hughes, A. Jacob, E.A. Jones, R. Kumar, R.J. Leventer, S. Macdonald, R. Maroofian, S.G. Mehta, I. Metz, E. Monfrini, D. Neumann, M. Noetzel, M. O'Driscoll, K. Ounap, A. Panzer, S. Parikh, P. Prabhakar, F. Ramond, R. Sandford, R. Saneto, C. Soh, C.A. Stutterd, G.M. Subramanian, K. Talbot, R.H. Thomas, C. Toro, R. Touraine, E. Wakeling, E. Wassmer, A. Whitney, J.H. Livingston, R.T. O'Keefe, A.P. Badrock
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
HOPS-associated neurological disorders (HOPSANDs): Linking endolysosomal dysfunction to the pathogenesis of dystonia
2021 E. Monfrini, M. Zech, D. Steel, M.A. Kurian, J. Winkelmann, A. Di Fonzo
Juvenile-onset dystonia with spasticity in Leigh syndrome caused by a novel NDUFA10 variant
2022 V. Yahya, F. Spagnolo, G. Di Maggio, E. Leopizzi, P. De Marco, F. Fortunato, G.P. Comi, A. Rini, E. Monfrini, A. Di Fonzo
Genetic evaluation in phenotypically discordant monozygotic twins with Coats Disease
2022 R.A.U. Lizzio, E. Monfrini, S. Romano, G. Brescia, S. Vujosevic, M. Sacchi, A. Di Fonzo, P. Nucci
Cognitive and Autonomic Dysfunction in Multiple System Atrophy Type P and C: A Comparative Study
2022 G. Lazzeri, G. Franco, T. Difonzo, A. Carandina, C. Gramegna, M. Vergari, F. Arienti, A. Naci, C. Scatà, E. Monfrini, G. Dias Rodrigues, N. Montano, G.P. Comi, M.C. Saetti, E. Tobaldini, 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
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
A Practical Approach to Early-Onset Parkinsonism
2022 G.M. Riboldi, E. Frattini, E. Monfrini, S.J. Frucht, A. Di Fonzo
Dysautonomia in Parkinson's Disease: Impact of Glucocerebrosidase Gene Mutations on Cardiovascular Autonomic Control
2022 A. Carandina, G. Lazzeri, G.D. Rodrigues, G. Franco, E. Monfrini, F. Arienti, E. Frattini, I. Trezzi, P.P. da Silva Soares, C. Bellocchi, L. Furlan, N. Montano, A. Di Fonzo, E. Tobaldini
Role of Lysosomal Gene Variants in Modulating GBA-Associated Parkinson's Disease Risk
2022 L. Straniero, V. Rimoldi, E. Monfrini, S. Bonvegna, G. Melistaccio, J. Lake, G. Solda, M. Aureli, Shankaracharya, P. Keagle, T. Foroud, J.E. Landers, C. Blauwendraat, A. Zecchinelli, R. Cilia, A. Di Fonzo, G. Pezzoli, S. Duga, R. Asselta
Role of Lysosomal Gene Variants in Modulating GBA-Associated Parkinson's Disease Risk
2022 L. Straniero, V. Rimoldi, E. Monfrini, S. Bonvegna, G. Melistaccio, J. Lake, G. Soldà, M. Aureli, N. Shankaracharya, P. Keagle, T. Foroud, J.E. Landers, C. Blauwendraat, A. Zecchinelli, R. Cilia, A. Di Fonzo, G. Pezzoli, S. Duga, R. Asselta
Clinical uses of Bupropion in patients with Parkinson’s disease and comorbid depressive or neuropsychiatric symptoms: a scoping review
2022 M.E.M. Vismara, B. Benatti, G. Nicolini, I. Cova, E. Monfrini, Alessio Di Fonzo, F. Vincenza, C.A. Vigano', A. Priori, D. Bernardo
THE ROLE OF NEXT-GENERATION SEQUENCING IN THE DISCOVERY OF NOVEL GENETIC CAUSES OF DYSTONIA
2022 E. Monfrini
Recent Advances in the Treatment of Genetic Forms of Parkinson’s Disease: Hype or Hope?
2023 F. Cavallieri, R.G. Cury, T. Guimaraes, V. Fioravanti, S. Grisanti, J. Rossi, E. Monfrini, M. Zedde, A. Di Fonzo, F. Valzania, E. Moro
Brain Calcifications: Genetic, Molecular, and Clinical Aspects
2023 E. Monfrini, F. Arienti, P. Rinchetti, F. Lotti, G.M. Riboldi
Genetic Evidence for Endolysosomal Dysfunction in Parkinson’s Disease: A Critical Overview
2023 V. Yahya, A. Di Fonzo, E. Monfrini
Case report: Asp194Ala variant in MFN2 is associated with ALS-FTD in an Italian family
2023 C. Vinciguerra, A. Di Fonzo, E. Monfrini, D. Ronchi, S. Cuoco, G. Piscosquito, P. Barone, M.T. Pellecchia
Speech, Gait, and Vestibular Function in Cerebellar Ataxia with Neuropathy and Vestibular Areflexia Syndrome
2023 G. Di Rauso, A. Castellucci, F. Cavallieri, A. Tozzi, V. Fioravanti, E. Monfrini, A. Gessani, J. Rossi, I. Campanini, A. Merlo, D. Ronchi, M. Napoli, R. Pascarella, S. Grisanti, G. Ferrulli, R. Sabadini, A. Di Fonzo, A. Ghidini, F. Valzania
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