MENERI, MEGI

MENERI, MEGI  

Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti  

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Risultati 1 - 20 di 41 (tempo di esecuzione: 0.006 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Unleashing the potential of mRNA therapeutics for inherited neurological diseases 2024 Monfrini, EdoardoBaso, GiacomoRonchi, DarioMeneri, MegiGagliardi, DeliaVerde, FedericoTicozzi, NicolaRatti, AntoniaComi, Giacomo POttoboni, LindaCorti, Stefania + Article (author) -
Shaping the Neurovascular Unit Exploiting Human Brain Organoids 2024 Rizzuti, MafaldaBrambilla, LorenzoOttoboni, LindaMeneri, MegiRatti, AntoniaVerde, FedericoTicozzi, NicolaComi, Giacomo PietroCorti, StefaniaAbati, Elena + Article (author) -
Proposal of a new clinical protocol for evaluating fatigability in adult SMA patients 2023 Ricci, GiuliaGovoni, AlessandraMagri, FrancescaMeneri, MegiComi, Giacomo + Article (author) -
Respiratory function in a large cohort of treatment-naïve adult spinal muscular atrophy patients: a cross-sectional study 2023 Govoni, AlessandraMeneri, MegiRicci, GiuliaTramacere, IreneComi, GiacomoMaggi, Lorenzo + Article (author) -
Correlation between clinical phenotype and electromyographic parameters in amyotrophic lateral sclerosis 2023 Scheveger, FrancescoMaranzano, AlessioGagliardi, DeliaMeneri, MegiVerde, FedericoMorelli, ClaudiaCorti, StefaniaSilani, VincenzoTicozzi, Nicola + Article (author) -
The impact of upper motor neuron involvement on clinical features, disease progression and prognosis in amyotrophic lateral sclerosis 2023 Gentile, FrancescoVerde, FedericoOlivero, MarcoGagliardi, DeliaMeneri, MegiPoletti, BarbaraCorti, StefaniaSilani, VincenzoTicozzi, Nicola + Article (author) -
Clinical and molecular features of patients with amyotrophic lateral sclerosis and SOD1 mutations: a monocentric study 2023 Gagliardi, DeliaMeneri, MegiDel Bo, RobertoComi, Giacomo PietroRatti, AntoniaTicozzi, NicolaSilani, VincenzoRonchi, DarioCorti, Stefania + Article (author) -
NOTCH2NLC GGC repeats are not expanded in Italian amyotrophic lateral sclerosis patients 2023 Manini, AriannaGagliardi, DeliaMeneri, MegiDel Bo, RobertoComi, Giacomo PietroCorti, StefaniaRonchi, Dario + Article (author) -
Multi-omics profiling of CSF from spinal muscular atrophy type 3 patients after nusinersen treatment: a 2-year follow-up multicenter retrospective study 2023 Faravelli, IreneGagliardi, DeliaAbati, ElenaMeneri, MegiMagri, FrancescaParente, ValeriaRicci, GiuliaGarrone, GiuliaFontana, ManuelaCaruso, DonatellaComi, Giacomo PietroGovoni, AlessandraCorti, StefaniaOttoboni, Linda + Article (author) -
Identification of Novel Biomarkers of Spinal Muscular Atrophy and Therapeutic Response by Proteomic and Metabolomic Profiling of Human Biological Fluid Samples 2023 Meneri, MegiAbati, ElenaGagliardi, DeliaRatti, AntoniaVerde, FedericoTicozzi, NicolaComi, Giacomo P.Ottoboni, LindaCorti, Stefania + Article (author) -
Unraveling the Neurological Complexity of Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal Protein, and Skin Changes Syndrome: A Report of a Challenging Case of a Young Woman and Cutting-Edge Advancements in the Field 2023 Furciniti, GiocondaLo Russo, Francesco MBolli, NiccolòMeneri, MegiComi, Giacomo PCorti, Stefania P + Article (author) -
A biallelic variant in COX18 cause isolated Complex IV deficiency associated with neonatal encephalo-cardio-myopathy and axonal sensory neuropathy 2023 Ronchi, DarioMagri, FrancescaMeneri, MegiDilena, RobertinoPicciolli, IreneSalani, SabrinaFortunato, FrancescoMosca, FabioCorti, StefaniaComi, Giacomo Pietro + Article (author) -
Regional spreading pattern is associated with clinical phenotype in amyotrophic lateral sclerosis 2023 Maranzano, AlessioVerde, FedericoColombo, EleonoraPoletti, BarbaraDoretti, AlbertoBonetti, RuggeroGagliardi, DeliaMeneri, MegiCorti, StefaniaMorelli, ClaudiaSilani, VincenzoTicozzi, Nicola + Article (author) -
Advancing Stroke Research on Cerebral Thrombi with Omic Technologies 2023 Costamagna, GianlucaBonato, SaraCorti, StefaniaMeneri, Megi Article (author) -
Adults with spinal muscular atrophy: a large-scale natural history study shows gender effect on disease 2022 Maggi, LorenzoGovoni, AlessandraMeneri, MegiRicci, GiuliaCorti, StefaniaComi, Giacomo + Article (author) -
New Insights into Cerebral Vessel Disease Landscapes at Single-Cell Resolution: Pathogenetic and Therapeutic Perspectives 2022 Meneri, MegiBonato, SaraGagliardi, DeliaComi, Giacomo PCorti, Stefania Article (author) -
Analysis of miRNA rare variants in amyotrophic lateral sclerosis and in silico prediction of their biological effects 2022 Ratti, AntoniaPeverelli, SilviaGentilini, DavideMeneri, MegiGagliardi, DeliaCorti, StefaniaLauria Pinter, GiuseppeTicozzi, NicolaSilani, Vincenzo + Article (author) -
Newly Diagnosed Hepatic Encephalopathy Presenting as Non-convulsive Status Epilepticus: A Case Report and Literature Review 2022 Olivero, MarcoGagliardi, DeliaCostamagna, GianlucaTriulzi, FabioConte, GiorgioComi, Giacomo PCorti, StefaniaMeneri, Megi + Article (author) -
Case Report: Rare Homozygous RNASEH1 Mutations Associated With Adult-Onset Mitochondrial Encephalomyopathy and Multiple Mitochondrial DNA Deletions 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 2022 Manini A.Meneri M.Corti S.Comi G. P.Ronchi D. + Article (author) -