MONZIO COMPAGNONI, GIACOMO

MONZIO COMPAGNONI, GIACOMO  

Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti  

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Risultati 1 - 10 di 10 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
ASSESSING THE PATHOGENESIS OF MULTIPLE SYSTEM ATROPHY THROUGH CELLULAR MODELS 16-gen-2018 G. MONZIO COMPAGNONI Doctoral Thesis -
Generation and characterization of iPSC-derived cortical pyramidal neurons from patients affected by multiple system atrophy 1-gen-2016 G. Monzio CompagnoniE. FrattiniS. SalaniF. FortunatoN. BresolinG.P. ComiS. CortiA. Di Fonzo Article (author) -
Loss of the nucleoporin Aladin in central nervous system and fibroblasts of Allgrove Syndrome 1-gen-2019 Ronchi, DarioBonato, SaraPittaro, AlessandraCompagnoni, Giacomo MonzioBordoni, AndreinaSalani, SabrinaFrattini, EmanueleLopez, GianlucaCorti, StefaniaComi, Giacomo PBresolin, Nereo + Article (author) -
Mitochondrial dysfunction in fibroblasts of Multiple System Atrophy 1-dic-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 13-nov-2018 Monzio Compagnoni GAureli MRonchi DFrattini EAbati ETabano SMiozzo MBresolin NCorti SDi Fonzo A + Article (author) -
Mutational analysis of COQ2 in patients with MSA in Italy 1-set-2016 D. RonchiG. FrancoR. Del BoF. FortunatoL. BorelliniI. TrezziG. Monzio CompagnoniE. MonfriniE. FrattiniS. BonatoA. PrioriN. BresolinS. CortiG.P. Comi + Article (author) -
Mutations in TMEM230 are rare in autosomal dominant Parkinson's disease 1-gen-2017 E. MonfriniG. FrancoI. TrezziL. BorelliniE. FrattiniD. RonchiG. Monzio CompagnoniF. CogiamanianG. ArdolinoN. BresolinG.P. ComiS. CortiA. Di Fonzo + Article (author) -
Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathy 1-mar-2019 Monfrini, EdoardoStraniero, LetiziaBonato, SaraMonzio Compagnoni, GiacomoBordoni, AndreinaRinchetti, PaolaSilipigni, RosamariaRonchi, DarioCorti, StefaniaComi, Giacomo P.Bresolin, NereoDuga, StefanoDi Fonzo, Alessio + Article (author) -
A novel homozygous PLA2G6 mutation causes dystonia-parkinsonism 1-mar-2015 E. MonfriniG. FrancoL. BorelliniI. TrezziG. Monzio CompagnoniD. RonchiS. BonatoN. BresolinS. CortiG.P. Comi + Article (author) -
The Role of Mitochondria in Neurodegenerative Diseases: the Lesson from Alzheimer’s Disease and Parkinson’s Disease 1-lug-2020 Monzio Compagnoni G.Corti S.Comi G. P.Bresolin N. + Article (author) -