MENERI, MEGI

MENERI, MEGI  

Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti  

Mostra records
Risultati 1 - 20 di 42 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Shaping the Neurovascular Unit Exploiting Human Brain Organoids 2024 Rizzuti, MafaldaBrambilla, LorenzoOttoboni, LindaMeneri, MegiRatti, AntoniaVerde, FedericoTicozzi, NicolaComi, Giacomo PietroCorti, StefaniaAbati, Elena + Article (author) -
Guanylate Kinase 1 Deficiency: A Novel and Potentially Treatable Mitochondrial DNA Depletion/Deletions Disease 2024 Meneri, MegiComi, Giacomo PietroRonchi, Dario + Article (author) -
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) -
Proposal of a new clinical protocol for evaluating fatigability in adult SMA patients 2023 Ricci, GiuliaGovoni, AlessandraMagri, FrancescaMeneri, MegiComi, Giacomo + 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) -
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) -
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) -
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) -
Advancing Stroke Research on Cerebral Thrombi with Omic Technologies 2023 Costamagna, GianlucaBonato, SaraCorti, StefaniaMeneri, Megi 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) -
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) -
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) -
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) -
Biallelic Variants in ENDOG Associated with Mitochondrial Myopathy and Multiple mtDNA Deletions 2022 Nasca A.Meneri M.Comi G. P.Catania A.Lamperti C.Ronchi D.Ghezzi D. + Article (author) -
Stathmins and Motor Neuron Diseases: Pathophysiology and Therapeutic Targets 2022 Delia GagliardiElisa PagliariMegi MeneriFederica RizzoGiacomo Pietro ComiStefania CortiMichela TaianaMonica Nizzardo + 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) -
Analysis of HTT CAG repeat expansion in Italian patients with amyotrophic lateral sclerosis 2022 Manini, AriannaGagliardi, DeliaMeneri, MegiDel Bo, RobertoComi, Giacomo PietroCorti, StefaniaRonchi, 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) -