DI FONZO, ALESSIO BARNABA

DI FONZO, ALESSIO BARNABA  

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Titolo Data di pubblicazione Autori Tipo File Abstract
Spinal direct current stimulation (tsDCS) in hereditary spastic paraplegias (HSP): A sham-controlled crossover study 2021 Ardolino, GianlucaBocci, TommasoDi Fonzo, AlessioBonato, SaraCogiamanian, FilippoCova, IlariaPriori, Alberto + Article (author) -
Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathy 2019 Monfrini, EdoardoStraniero, LetiziaBonato, SaraMonzio Compagnoni, GiacomoBordoni, AndreinaRinchetti, PaolaSilipigni, RosamariaRonchi, DarioCorti, StefaniaComi, Giacomo P.Bresolin, NereoDuga, StefanoDi Fonzo, Alessio + Article (author) -
The length of SNCA Rep1 microsatellite may influence cognitive evolution in Parkinson's disease 2018 Corrado, LuciaTUNESI, SARAFonzo, Alessio DiTrezzi, IlariaComi, Giacomo P. + Article (author) -
Mitochondrial dysfunction in fibroblasts of Multiple System Atrophy 2018 Monzio Compagnoni, GiacomoBordoni, AndreinaFortunato, FrancescoRonchi, DarioSalani, SabrinaREALE, CHIARACogiamanian, FilippoArdolino, GianlucaBresolin, NereoCorti, StefaniaComi, Giacomo P.Di Fonzo, Alessio + Article (author) -
Mitochondrial Dysregulation and Impaired Autophagy in iPSC-Derived Dopaminergic Neurons of Multiple System Atrophy 2018 Monzio Compagnoni GAureli MRonchi DFrattini EAbati ETabano SMiozzo MBresolin NCorti SDi Fonzo A + Article (author) -
Real life evaluation of safinamide effectiveness in Parkinson’s disease 2018 Di Fonzo, AlessioBorellini, LindaSilani, Vincenzo + Article (author) -
Clinical reasoning: a 75-year-old man with parkinsonism, mood depression, and weight loss 2018 Frattini E.Monfrini E.Arcudi S.Bresolin N.Saetti M. C.Di Fonzo A. + Article (author) -
Syncope and autonomic failure in a middle-aged man 2018 COLOMBO, GIORGIOFrattini, EmanueleCeriani, ElisaZilocchi, MassimoDel Bo, RobertoDi Fonzo, AlessioSolbiati, Monica Article (author) -
The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p 2017 L. StranieroV. RimoldiM. SamaraniA. Di FonzoM. AureliG. SoldàS. DugaR. Asselta + Article (author) -
Globus pallidus internus deep brain stimulation in PINK-1 related Parkinson's disease: A case report 2017 Borellini, LindaCogiamanian, FilippoCarrabba, GiorgioLocatelli, MarcoDi Fonzo, AlessioBana, CristinaArdolino, Gianluca + 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) -
A de novo C19orf12 heterozygous mutation in a patient with MPAN 2017 E. MonfriniD. RonchiR. DilenaA. BordoniN. BresolinG. P. ComiS. CortiA. Di Fonzo + Article (author) -
X-linked Parkinsonism with Intellectual Disability caused by novel mutations and somatic mosaicism in RAB39B gene 2017 A..B. Di FonzoVILLA, ROBERTAB. PolettiE. MonfriniV. SilaniC..M. Cinnante + 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) -
Generation and characterization of iPSC-derived cortical pyramidal neurons from patients affected by multiple system atrophy 2016 G. Monzio CompagnoniE. FrattiniS. SalaniF. FortunatoN. BresolinG.P. ComiS. CortiA. Di Fonzo Article (author) -
Autophagy in motor neuron disease: Key pathogenetic mechanisms and therapeutic targets 2016 S. BrajkovicE. FrattiniA. Di FonzoS. Corti + Article (author) -
Adaptive deep brain stimulation in a freely moving parkinsonian patient 2015 M. RosaF. CogiamanianS. MarcegliaA. Di FonzoA. Priori + Article (author) -
Unusual adult-onset Leigh syndrome presentation due to the mitochondrial m.9176T > C mutation 2011 D. RonchiA. BordoniCOSI, ALESSANDRAE. FassoneA. Di FonzoM. ServidaV. LucchiniM. MattioliN. BresolinS. CortiG. Comi + Article (author) -
A novel MAPT mutation associated to late-onset spinal muscular atrophy without dementia in a large Italian family 2011 D. RonchiA. Di FonzoE. FassoneS. SalaniA. BordoniR. Del BoS. CortiE. Nobile-OrazioG.P. Comi + Conference Object -
Two novel mutations in PEO1 (twinkle) gene associated with chronic external ophthalmoplegia 2011 D. RonchiE. FassoneA. BordoniV. LucchiniA. Di FonzoI. ColomboA. CosiS. CortiN. BresolinG.P. Comi + Article (author) -