ARIENTI, FEDERICA
ARIENTI, FEDERICA
Universita' degli Studi di MILANO
Brain Calcifications: Genetic, Molecular, and Clinical Aspects
2023 E. Monfrini, F. Arienti, P. Rinchetti, F. Lotti, G.M. Riboldi
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
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
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
Effective Connectivity During Rest and Music Listening : An EEG Study on Parkinson’s Disease
2021 E. Maggioni, F. Arienti, S. Minella, F. Mameli, L. Borellini, M. Nigro, F. Cogiamanian, A.M. Bianchi, S. Cerutti, S. Barbieri, P. Brambilla, G. Ardolino
Late-onset leukoencephalopathy in a patient with recessive EARS2 mutations
2020 E. Monfrini, D. Ronchi, G. Franco, M. Garbellini, L. Straniero, E. Scola, F. Arienti, S. Duga, G.P. Comi, N. Bresolin, A. Di Fonzo
Systemic involvement in adult-onset leukoencephalopathy with intracranial calcifications and cysts (Labrune syndrome) with a novel mutation of the SNORD118 gene
2020 G. Bonomo, E. Monfrini, L. Borellini, R. Bonomo, F. Arienti, M.C. Saetti, A. Di Fonzo, M. Locatelli
Microscopic Polyangiitis With Selective Involvement of Central and Peripheral Nervous System : A Case Report
2020 F. Arienti, G. Franco, E. Monfrini, A. Santaniello, N. Bresolin, M.C. Saetti, A. Di Fonzo