MAGRI, FRANCESCA MARIA BENEDETTA

MAGRI, FRANCESCA MARIA BENEDETTA  

Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti  

Mostra records
Risultati 1 - 20 di 159 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Opinion of the Italian Association of Myology on Ataluren for the Treatment of Nonsense Mutation Duchenne Muscular Dystrophy 2025 Bruno, ClaudioCorti, StefaniaD'Angelo, Maria GraziaMaggi, LorenzoMagri, FrancescaRicci, GiuliaSansone, ValeriaComi, Giacomo P + Article (author) -
Case report: A novel ACTA1 variant in a patient with nemaline rods and increased glycogen deposition 2024 Magri, FrancescaComi, Giacomo PietroRonchi, DarioCorti, Stefania + Article (author) -
Myotonic Dystrophy type 2 unmasked by physical activity resumption following COVID-19 lockdown: case discussion and review of the literature 2024 Lucchiari, SabrinaMagri, FrancescaPagliarani, SerenaCorti, StefaniaComi, Giacomo P + Article (author) -
Prevalence of Duchenne muscular dystrophy in Italy: a nationwide survey 2024 Sansone, Valeria AdaComi, GiacomoMagri, Francesca + Article (author) -
Clinical, Histopathologic, and Genetic Features of Patients With Myofibrillary and Distal Myopathies: Experience From the Italian Network 2024 Magri, FrancescaRicci, GiuliaComi, Giacomo PMaggi, Lorenzo + Article (author) -
Case report: A novel patient presenting TRIM32-related limb-girdle muscular dystrophy 2023 Romagnoli, GloriaMagri, FrancescaCinnante, ClaudiaCorti, StefaniaComi, Giacomo PietroRonchi, 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) -
Prominent muscle involvement in a familial form of mitochondrial disease due to a COA8 variant 2023 Magri, FrancescaRipolone, MichelaSalani, SabrinaFortunato, FrancescoCorti, StefaniaComi, Giacomo PietroRonchi, Dario + Article (author) -
NGS-Based Genetic Analysis in a Cohort of Italian Patients with Suspected Inherited Myopathies and/or HyperCKemia 2023 Lamantea E.Peverelli L.Magri F.Comi G. P.Ronchi D.Ghezzi D.Lamperti C. + Article (author) -
Using Cluster Analysis to Overcome the Limits of Traditional Phenotype-Genotype Correlations: The Example of RYR1-Related Myopathies 2023 Comi, Giacomo PietroMagri, Francesca + Article (author) -
Cognitive abnormalities in Becker muscular dystrophy: a mysterious link between dystrophin deficiency and executive functions 2023 Pezzoni, LauraBrusa, RobertaMagri, FrancescaCorti, StefaniaComi, Giacomo PietroSaetti, Maria Cristina + Article (author) -
Givinostat for Becker muscular dystrophy: A randomized, placebo-controlled, double-blind study 2023 Comi, Giacomo PMagri, Francesca + Article (author) -
Proposal of a new clinical protocol for evaluating fatigability in adult SMA patients 2023 Ricci, GiuliaGovoni, AlessandraMagri, FrancescaMeneri, MegiComi, Giacomo + Article (author) -
The Profiling of 179 miRNA Expression in Serum from Limb Girdle Muscular Dystrophy Patients and Healthy Controls 2023 Magri, FrancescaRipolone, MichelaCorti, StefaniaComi, Giacomo Pietro + Article (author) -
Genetic modifiers of upper limb function in Duchenne muscular dystrophy 2022 D'Angelo, GraziaMagri, FrancescaComi, Giacomo PBruno, Claudio + Article (author) -
Age, corticosteroid treatment and site of mutations affect motor functional changes in young boys with Duchenne Muscular Dystrophy 2022 Bello L.Magri F.Comi G. P.Sansone V. A.De Luca G. + Article (author) -
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study 2022 Magri F.Pane M.Bello L.Bernasconi P.Comi G.Nigro V.Minervini G. + Article (author) -
Muscle histological changes in a large cohort of patients affected with Becker muscular dystrophy 2022 Ripolone M.Magri F.Fortunato F.Comi G. P. + Article (author) -
Antisense Morpholino-Based In Vitro Correction of a Pseudoexon-Generating Variant in the SGCB Gene 2022 Magri, FrancescaSalani, SabrinaFortunato, FrancescoMaggi, LorenzoCorti, StefaniaBresolin, NereoComi, Giacomo PietroRonchi, Dario + Article (author) -
Impact of COVID-19 on the quality of life of patients with neuromuscular disorders in the Lombardy area, Italy 2021 Gagliardi, DeliaCostamagna, GianlucaAbati, ElenaMauri, EleonoraBrusa, RobertaAndreoli, LucaCitterio, GaiaMagri, FrancescaMeneri, MegiBresolin, NereoCorti, StefaniaComi, Giacomo Pietro + Article (author) -