MAGRI, FRANCESCA MARIA BENEDETTA

MAGRI, FRANCESCA MARIA BENEDETTA  

Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti  

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Titolo Data di pubblicazione Autori Tipo File Abstract
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) -
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) -
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) -
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) -
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) -
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) -
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) -
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) -
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) -
Genetic modifiers of upper limb function in Duchenne muscular dystrophy 2022 D'Angelo, GraziaMagri, FrancescaComi, Giacomo PBruno, Claudio + Article (author) -
Onasemnogene abeparvovec gene therapy for symptomatic infantile-onset spinal muscular atrophy type 1 (STR1VE-EU): an open-label, single-arm, multicentre, phase 3 trial 2021 Corti S.Magri F.Comi G. + 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) -
North Star Ambulatory Assessment changes in ambulant Duchenne boys amenable to skip exons 44, 45, 51, and 53 : A 3 year follow up 2021 Magri F.Comi G. P.Sansone V. A. + Article (author) -
Missense mutations in small muscle protein X-linked (SMPX) cause distal myopathy with protein inclusions 2021 Magri F.Mauri E.Comi G. P. + Article (author) -
The nonsense mutation stop+4 model correlates with motor changes in Duchenne muscular dystrophy 2021 Magri FPedemonte MBello LPolitano LComi GPSansone VA + Article (author) -
CACNA1S mutation associated with a case of juvenile-onset congenital myopathy 2021 Mauri E.Pagliarani S.Magri F.Manini A.Ripolone M.Borellini L.Cinnante C.Corti S.Bresolin N.Comi G. P. + Article (author) -
Early Findings in Neonatal Cases of RYR1-Related Congenital Myopathies 2021 Mauri, EleonoraGovoni, AlessandraBrusa, RobertaPagliarani, SerenaRipolone, MichelaCinnante, ClaudiaBresolin, NereoCorti, StefaniaComi, Giacomo PMagri, Francesca + Article (author) -
Diagnostic and prognostic value of CSF neurofilaments in a cohort of patients with motor neuron disease: A cross-sectional study 2021 Gagliardi, DeliaFaravelli, IreneMeneri, MegiGovoni, AlessandraMagri, FrancescaPietro Comi, GiacomoCorti, Stefania + Article (author) -