FRATTINI, EMANUELE

FRATTINI, EMANUELE  

Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti  

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Risultati 1 - 13 di 13 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Autophagy in motor neuron disease: Key pathogenetic mechanisms and therapeutic targets 1-gen-2016 S. BrajkovicE. FrattiniA. Di FonzoS. Corti + Article (author) -
Clinical reasoning: a 75-year-old man with parkinsonism, mood depression, and weight loss 20-mar-2018 Frattini E.Monfrini E.Arcudi S.Bresolin N.Saetti M. C.Di Fonzo A. + Article (author) -
Expanding the genotypic and phenotypic spectrum of Beta-propeller-associated neurodegeneration (BPAN) 1-gen-2021 Monfrini, EdoardoBonato, SaraFrattini, EmanueleFranco, GiuliaCorti, StefaniaComi, Giacomo PietroBresolin, Nereo + Article (author) -
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) -
iPSC-Based Models to Unravel Key Pathogenetic Processes Underlying Motor Neuron Disease Development 17-ott-2014 I. FaravelliE. FrattiniA. RamirezM. NizzardoS. Corti + 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 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) -
Motor neuron derivation from human embryonic and induced pluripotent stem cells: experimental approaches and clinical perspectives 1-gen-2014 I. FaravelliM. BucchiaP. RinchettiM. NizzardoC. SimoneE. FrattiniS. Corti 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) -
Pluripotent stem cell-based models of spinal muscular atrophy 1-gen-2015 E. FrattiniS. SalaniI. FaravelliM. NizzardoC. SimoneF. MagriS. Corti + Article (author) -
Spinal muscular atrophy phenotype is ameliorated in human motor neurons by SMN increase via different novel RNA therapeutic approaches 1-gen-2015 M. NizzardoC. SimoneS. DamettiS. SalaniG. UlziS. PagliaraniF. RizzoE. FrattiniN. BresolinG. ComiS. Corti + Article (author) -
Syncope and autonomic failure in a middle-aged man 15-mag-2018 COLOMBO, GIORGIOFrattini, EmanueleCeriani, ElisaZilocchi, MassimoDel Bo, RobertoDi Fonzo, AlessioSolbiati, Monica Article (author) -