FRANCO, GIULIA

FRANCO, GIULIA  

Universita' degli Studi di MILANO  

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Risultati 1 - 15 di 15 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Supplementing Best Care with Specialized Rehabilitation Treatment in Parkinson’s Disease: A Retrospective Study by Different Expert Centers 2024 Castelli, DavideFranco, GiuliaFrattini, Emanuele + Article (author) -
Verbal Learning Impairment in Parkinson's Disease: Role of the Frontostriatal System in Working and Strategic Memory 2023 Cocuzza, AlessandroSbrissa, Luca Pietro ErnestoZago, StefanoGendarini, ClaudiaPoletti, BarbaraTicozzi, NicolaFranco, GiuliaComi, Giacomo PietroSaetti, Maria Cristina + Article (author) -
Dysautonomia in Parkinson's Disease: Impact of Glucocerebrosidase Gene Mutations on Cardiovascular Autonomic Control 2022 Carandina, AngelicaLazzeri, GiuliaRodrigues, Gabriel DiasFranco, GiuliaMonfrini, EdoardoArienti, FedericaFrattini, EmanueleTrezzi, IlariaBellocchi, ChiaraFurlan, LudovicoMontano, NicolaTobaldini, Eleonora + Article (author) -
Cognitive and Autonomic Dysfunction in Multiple System Atrophy Type P and C: A Comparative Study 2022 Lazzeri, GiuliaFranco, GiuliaCarandina, AngelicaArienti, FedericaNaci, AnisaMonfrini, EdoardoDias Rodrigues, GabrielMontano, NicolaComi, Giacomo PSaetti, Maria CristinaTobaldini, Eleonora + Article (author) -
TWNK in Parkinson's Disease: A Movement Disorder and Mitochondrial Disease Center Perspective Study 2022 Percetti, MarcoFranco, GiuliaMonfrini, EdoardoVizziello, MariaRonchi, DarioDi Berardino, FedericaCocco, AntoniangelaComi, Giacomo Pietro + Article (author) -
Expanding the genotypic and phenotypic spectrum of Beta-propeller-associated neurodegeneration (BPAN) 2021 Monfrini, EdoardoBonato, SaraFrattini, EmanueleFranco, GiuliaCorti, StefaniaComi, Giacomo PietroBresolin, Nereo + Article (author) -
Unravelling Genetic Factors Underlying Corticobasal Syndrome: A Systematic Review 2021 Arienti, FedericaLazzeri, GiuliaVizziello, MariaMonfrini, EdoardoBresolin, NereoSaetti, Maria CristinaFranco, Giulia + Article (author) -
A case report of late-onset cerebellar ataxia associated with a rare p.R342W TGM6 (SCA35) mutation 2020 Manini, AriannaBocci, TommasoMonfrini, EdoardoRonchi, DarioFranco, GiuliaDe Rosa, AnnaPriori, AlbertoCorti, StefaniaComi, Giacomo PietroBresolin, NereoBasso, Manuela + Article (author) -
Late-onset leukoencephalopathy in a patient with recessive EARS2 mutations 2020 Edoardo MonfriniDario RonchiGiulia FrancoLetizia StranieroFederica ArientiStefano DugaGiacomo Pietro ComiNereo Bresolin + Article (author) -
Microscopic Polyangiitis With Selective Involvement of Central and Peripheral Nervous System : A Case Report 2020 Arienti F.Franco G.Monfrini E.Santaniello A.Bresolin N.Saetti M. C. + Article (author) -
Progressive encephalomyelitis with rigidity and myoclonus associated with anti-GlyR antibodies and Hodgkin's lymphoma : A case report 2017 Borellini, LindaLanfranconi, SilviaBonato, SaraTrezzi, IlariaFranco, GiuliaBresolin, NereoDi Fonzo, Alessio Barnaba + Article (author) -
Mutations in TMEM230 are rare in autosomal dominant Parkinson's disease 2017 E. MonfriniG. FrancoI. TrezziL. BorelliniE. FrattiniD. RonchiG. Monzio CompagnoniF. CogiamanianG. ArdolinoN. BresolinG.P. ComiS. CortiA. Di Fonzo + Article (author) -
Mutational analysis of COQ2 in patients with MSA in Italy 2016 D. RonchiG. FrancoR. Del BoF. FortunatoL. BorelliniI. TrezziG. Monzio CompagnoniE. MonfriniE. FrattiniS. BonatoA. PrioriN. BresolinS. CortiG.P. Comi + Article (author) -
A novel homozygous PLA2G6 mutation causes dystonia-parkinsonism 2015 E. MonfriniG. FrancoL. BorelliniI. TrezziG. Monzio CompagnoniD. RonchiS. BonatoN. BresolinS. CortiG.P. Comi + Article (author) -
Optic neuritis as isolated manifestation of leptomeningeal carcinomatosis : a case report and systematic review of ocular manifestations of neoplastic meningitis 2013 S. LanfranconiP. BasilicoI. TrezziL. BorelliniG. FrancoN. Bresolin + Article (author) -