BORDONI, ANDREINA

BORDONI, ANDREINA  

Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti  

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Risultati 1 - 20 di 125 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Cell Penetrating peptide-conjugated Morpholino rescues SMA in a symptomatic preclinical model 2020 Pagliari E.Bersani M.Rizzuti M.Bordoni A.Bresolin N.Comi G. P.Corti S.Nizzardo M. + Conference Object -
CPPs-conjugated antisense nucleotides : a new therapeutic strategy for Spinal Muscular Atrophy symptomatic patients 2020 E. PagliariM. BersaniM. RizzutiA. BordoniN. BresolinGP. ComiS. CortiM. Nizzardo + Conference Object -
Dystonia-ataxia syndrome with permanent torsional nystagmus caused by ECHS1 deficiency 2020 Ronchi, DarioMonfrini, EdoardoBonato, SaraCinnante, ClaudiaSalani, SabrinaBordoni, AndreinaFortunato, FrancescoCorti, StefaniaBresolin, NereoComi, Giacomo P + Article (author) -
CPPs-conjugated antisense nucleotides : a new therapeutic strategy for Spinal Muscular Atrophy symptomatic patients 2019 Pagliari E.Bersani M.Rizzuti M.Bordoni A.Comi GP.Corti S.Nizzardo M. Conference Object -
Loss of the nucleoporin Aladin in central nervous system and fibroblasts of Allgrove Syndrome 2019 Ronchi, DarioBonato, SaraPittaro, AlessandraCompagnoni, Giacomo MonzioBordoni, AndreinaSalani, SabrinaFrattini, EmanueleLopez, GianlucaCorti, StefaniaComi, Giacomo PBresolin, Nereo + Article (author) -
Key role of SMN/SYNCRIP and RNA-Motif 7 in spinal muscular atrophy: RNA-Seq and motif analysis of human motor neurons 2019 Rizzo, FedericaNizzardo, MonicaVashisht, ShikhaMolteni, ErikaTaiana, MichelaSalani, SabrinaBucchia, MonicaBordoni, AndreinaFaravelli, IreneBresolin, NereoComi, Giacomo PietroCorti, Stefania + 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) -
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) -
Glucose-free/high-protein diet improves hepatomegaly and exercise intolerance in glycogen storage disease type III mice 2018 Pagliarani, SerenaLucchiari, SabrinaFortunato, FrancescoBordoni, AndreinaCorti, StefaniaBresolin, NereoComi, Giacomo P. + 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) -
Genome-wide RNA-seq and proteomic analysis of motor neurons indicates selective cytoskeletal perturbation in Brown-Vialetto disease, partially rescued by riboflavin 2017 F. RizzoA. RamirezS. SalaniA. BordoniF. FortunatoN. BresolinG.P. ComiM. NizzardoS. Corti + Article (author) -
Effects of short-to-long term enzyme replacement therapy (ERT) on skeletal muscle tissue in late onset Pompe disease (LOPD) 2017 D. RonchiA. BordoniF. FortunatoG.P. Comi + Article (author) -
Longitudinal follow-up and muscle MRI pattern of two siblings with polyglucosan body myopathy due to glycogenin-1 mutation 2016 I. ColomboS. PagliaraniC.M. CinnanteA. BordoniF. FortunatoF. MagriG.P. Comi + Article (author) -
Morpholino-mediated SOD1 reduction ameliorates an amyotrophic lateral sclerosis disease phenotype 2016 M. NizzardoC. SimoneF. RizzoG. UlziA. RamirezA. BordoniM. BucchiaN. BresolinG.P. ComiS. Corti + Article (author) -
Changes in whole-body oxygen consumption and skeletal muscle mitochondria during linezolid-induced lactic acidosis 2016 A. ProttiD. RonchiG. BassiF. FortunatoA. Bordoni + Article (author) -
Selective mitochondrial depletion, apoptosis resistance, and increased mitophagy in human Charcot-Marie-Tooth 2A motor neurons 2016 RIZZO, FEDERICAD. RonchiS. SalaniM. NizzardoF. FortunatoA. BordoniR. Del BoN. BresolinG.P. ComiS. Corti + Article (author) -
Morpholino antisense oligomer against SOD1 for amyotrophic lateral sclerosis therapy 2015 F. RizzoG. UlziA. RamirezM. BucchiaA. BordoniG. ComiS. Corti + Conference Object -
Adult polyglucosan body disease: clinical and histological heterogeneity of a large Italian family 2015 S. PagliaraniA. BordoniS. SalaniG.P. Comi + Article (author) -
Impaired muscle mitochondrial biogenesis and myogenesis in spinal muscular atrophy 2015 M. RipoloneD. RonchiV. LucchiniI. ColomboL. VillaA. BordoniF. FortunatoS. CortiG.P. Comi + Article (author) -
Extended phenotype description and new molecular findings in late onset glycogen storage disease type II: a northern Italy population study and review of the literature 2014 D. RonchiF. MagriC. LampertiA. BordoniN. BresolinG.P. Comi + Article (author) -