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
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) -
Guanylate Kinase 1 Deficiency: A Novel and Potentially Treatable Mitochondrial DNA Depletion/Deletions Disease 2024 Meneri, MegiComi, Giacomo PietroRonchi, Dario + 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) -
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) -
Proposal of a new clinical protocol for evaluating fatigability in adult SMA patients 2023 Ricci, GiuliaGovoni, AlessandraMagri, FrancescaMeneri, MegiComi, Giacomo + 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) -
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) -
Advancing Stroke Research on Cerebral Thrombi with Omic Technologies 2023 Costamagna, GianlucaBonato, SaraCorti, StefaniaMeneri, Megi 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) -
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) -
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) -
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) -
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) -
Correlation between clinical phenotype and electromyographic parameters in amyotrophic lateral sclerosis 2023 Scheveger, FrancescoMaranzano, AlessioGagliardi, DeliaMeneri, MegiVerde, FedericoMorelli, ClaudiaCorti, StefaniaSilani, VincenzoTicozzi, Nicola + 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) -
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) -
Insights into the identification of a molecular signature for amyotrophic lateral sclerosis exploiting integrated microRNA profiling of iPSC-derived motor neurons and exosomes 2022 Rizzuti M.Gagliardi D.Meneri M.Dioni L.Locatelli M.Biella F.Bollati V.Bresolin N.Comi G. P.Corti S. + 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) -
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) -
Homozygous SOD1 Variation L144S Produces a Severe Form of Amyotrophic Lateral Sclerosis in an Iranian Family 2022 Gagliardi, DeliaDel Bo, RobertoMeneri, MegiComi, Giacomo PietroCorti, StefaniaRonchi, Dario + Article (author) -