MANINI, ARIANNA

MANINI, ARIANNA  

Mostra records
Risultati 1 - 19 di 19 (tempo di esecuzione: 0.007 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
A case report of late-onset cerebellar ataxia associated with a rare p.R342W TGM6 (SCA35) mutation 7-nov-2020 Manini, AriannaBocci, TommasoMonfrini, EdoardoRonchi, DarioFranco, GiuliaDe Rosa, AnnaPriori, AlbertoCorti, StefaniaComi, Giacomo PietroBresolin, NereoBasso, Manuela + Article (author) -
A cross-sectional survey study of the impact of COVID-19 pandemic on the training and quality of life of Italian medical residents in the Lombardy region 1-dic-2022 Abati, ElenaNelva Stellio, LeonardoManini, Arianna + Article (author) -
A novel RRM2B mutation associated with mitochondrial DNA depletion syndrome 1-set-2022 Fumagalli, MonicaRonchi, DarioManini, AriannaMosca, FabioDilena, RobertinoTriulzi, FabioCorti, StefaniaComi, Giacomo P + Article (author) -
Adeno-Associated Virus (AAV)-mediated gene therapy for Duchenne muscular dystrophy : the issue of transgene persistence 5-gen-2022 Manini A.Abati E.Corti S.Comi G. P. + Article (author) -
Analysis of HTT CAG repeat expansion in Italian patients with amyotrophic lateral sclerosis 1-nov-2022 Manini, AriannaGagliardi, DeliaMeneri, MegiDel Bo, RobertoComi, Giacomo PietroCorti, StefaniaRonchi, Dario + Article (author) -
Association of the risk factor UNC13A with survival and upper motor neuron involvement in amyotrophic lateral sclerosis 1-feb-2023 Manini, AriannaCasiraghi, ValeriaBonetti, RuggeroVerde, FedericoPoletti, BarbaraSilani, VincenzoRatti, AntoniaTicozzi, Nicola + Article (author) -
CACNA1S mutation associated with a case of juvenile-onset congenital myopathy 1-gen-2021 Mauri E.Pagliarani S.Magri F.Manini A.Ripolone M.Borellini L.Cinnante C.Corti S.Bresolin N.Comi G. P. + Article (author) -
Case Report: Rare Homozygous RNASEH1 Mutations Associated With Adult-Onset Mitochondrial Encephalomyopathy and Multiple Mitochondrial DNA Deletions 1-gen-2022 Manini, AriannaMeneri, MegiCorti, StefaniaComi, Giacomo PietroRonchi, Dario + Article (author) -
Case Report: Thymidine Kinase 2 (TK2) Deficiency: A Novel Mutation Associated With Childhood-Onset Mitochondrial Myopathy and Atypical Progression 1-gen-2022 Manini A.Meneri M.Corti S.Comi G. P.Ronchi D. + Article (author) -
Clinical and genetic features of a cohort of patients with MFN2-related neuropathy 13-apr-2022 Abati E.Manini A.Del Bo R.Rizzo F.Bresolin N.Bellone E.Bassi M. T.D'Angelo M. G.Comi G. P.Corti S. + Article (author) -
Etiologic reclassification of cryptogenic stroke after implantable cardiac monitoring and computed tomography angiography re-assessment 13-set-2022 Mele, FrancescoScopelliti, GiuseppeManini, AriannaFerrari Aggradi, CarolaSchiavone, MarcoIanniello, AndreaBertora, PierluigiPantoni, Leonardo + Article (author) -
Expanding the Phenotypic Spectrum of Vocal Cord and Pharyngeal Weakness With Distal Myopathy due to the p.S85C MATR3 Mutation 1-ago-2022 Manini, AriannaCinnante, ClaudiaComi, GiacomoCorti, StefaniaRonchi, Dario + Article (author) -
Inhibition of myostatin and related signaling pathways for the treatment of muscle atrophy in motor neuron diseases 21-giu-2022 Abati, ElenaManini, AriannaComi, Giacomo PietroCorti, Stefania Article (author) -
NOTCH2NLC GGC repeats are not expanded in Italian amyotrophic lateral sclerosis patients 23-feb-2023 Manini, AriannaGagliardi, DeliaMeneri, MegiDel Bo, RobertoComi, Giacomo PietroCorti, StefaniaRonchi, Dario + Article (author) -
Phenotypic correlates of serum neurofilament light chain levels in amyotrophic lateral sclerosis 15-mar-2023 Verde, FedericoGentile, FrancescoManini, AriannaBonetti, RuggeroPoletti, BarbaraRatti, AntoniaSilani, VincenzoTicozzi, Nicola + Article (author) -
Rapidly progressive dementia and intractable diarrhea: a teaching case report and a systematic review of cognitive impairment in Whipple's disease 1-feb-2022 Manini, AriannaQuerzola, GiacomoLovati, CarloPantoni, Leonardo Article (author) -
Serum levels of glial fibrillary acidic protein in patients with amyotrophic lateral sclerosis 1-gen-2023 Verde, FedericoMilone, IlariaGentile, FrancescoManini, AriannaBonetti, RuggeroPoletti, BarbaraRatti, AntoniaSilani, VincenzoTicozzi, Nicola + Article (author) -
The impact of lockdown during SARS-CoV-2 outbreak on behavioral and psychological symptoms of dementia 1-gen-2021 Manini A.Maggiore L.Pomati S.Pantoni L. + Article (author) -
TMEM106B Acts as a Modifier of Cognitive and Motor Functions in Amyotrophic Lateral Sclerosis 1-ago-2022 Manini A.Ratti A.Maranzano A.Gentilini D.Verde F.Poletti B.Silani V.Ticozzi N. + Article (author) -