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
24 month longitudinal data in ambulant boys with Duchenne muscular dystrophy 11-gen-2013 Y. TorrenteF. MagriG.P. Comi + Article (author) -
6 minute walk test in duchenne MD patients with different mutations : 12 month changes 8-gen-2014 Y. TorrenteF. MagriG.P. Comi + Article (author) -
A model for motor neuron degeneration and treatment of Spinal Muscular Atrophy using human induced pluripotent stem cells 1-gen-2011 S. CortiF. MagriM. NizzardoC. SimoneM. FalconeS. SalaniC. DonadoniM. NardiniRIBOLDI, GIOVANNAF. RizzoN. BresolinG. Comi + Article (author) -
A new case of limb girdle muscular dystrophy 2G in a Greek patient, founder effect and review of the literature 1-giu-2018 Brusa, RobertaMagri, FrancescaPapadimitriou, DimitraGovoni, AlessandraDel Bo, RobertoCinnante, ClaudiaCorti, StefaniaBresolin, NereoComi, Giacomo Pietro + Article (author) -
A novel CHRNE gene mutation associated with congenital myasthenia: case report and review of the literature 1-gen-2010 F. MagriA. GovoniR. Del BoN. BresolinG.P. ComiS. Corti + Conference Object -
A novel GENE mutations causes familial recessive myopathy without inclusion bodies 1-gen-2006 R. Del BoM. GuglieriF. MagriN. BresolinG.P. Comi + Article (author) -
A novel intronic DYS gene mutation leading to a pseudoexon insertion in a DMD patient 1-gen-2010 A. GovoniF. MagriR. Del BoF. FortunatoG.P. Comi + Conference Object -
A novel splice-site mutation in SMN1 resulting in a very severe SMA1 phenotype 1-gen-2014 D. RonchiF. MagriS. CortiG.P. Comi + Article (author) -
A stop codon mutation in the 5’ of the dystrophin gene associated to a Becker muscular dystrophy phenotype 1-giu-2008 F. MagriR. VirgilioR. Del BoF. FortunatoR. CaglianiM. SironiV. CrugnolaN. BresolinG.P. Comi + Article (author) -
Adult Form Type II Glycogen Storage Disease in a Northern Italy Population : Phenotype Characterization, Early Diagnosis and Prognostic Determinants 1-gen-2009 D. RonchiC. LampertiA. BordoniF. MagriN. BresolinG. P. Comi + Article (author) -
Adult form type II Glycogen Storage Disease in a Northern Italy population :_phenotype, charatcerization, early diagnosis and prognostic determinants 1-gen-2008 D. RonchiC. LampertiM.G. D'AngeloA. BordoniF. MagriN. BresolinG.P. Comi + Article (author) -
Age, corticosteroid treatment and site of mutations affect motor functional changes in young boys with Duchenne Muscular Dystrophy 1-gen-2022 Bello L.Magri F.Comi G. P.Sansone V. A.De Luca G. + Article (author) -
Analisi molecolare del gene GAA e caratterizzazione di due nuove mutazioni di splicing in pazienti con deficit di maltasi acida. 1-gen-2008 D. RonchiA. BordoniE. FassoneF. MagriG.P. ComiM. Nizzardo + Conference Object -
Anti-sulfatide reactivity in patients with celiac disease 1-gen-2017 C. TombaF. MagriL. RoncoroniL. DonedaM.T. BardellaG.P. ComiN. BresolinD. ConteL. Elli + Article (author) -
Antisense Morpholino-Based In Vitro Correction of a Pseudoexon-Generating Variant in the SGCB Gene 29-ago-2022 Magri, FrancescaSalani, SabrinaFortunato, FrancescoMaggi, LorenzoCorti, StefaniaBresolin, NereoComi, Giacomo PietroRonchi, Dario + Article (author) -
Antisense Oligonucleotide Therapy for the Treatment of C9ORF72 ALS/FTD Diseases 28-apr-2014 G. RiboldiM. RanieriM. NizzardoC. SimoneF. MagriN. BresolinG.P. ComiS. Corti + Article (author) -
Autosomal dominant and recessive limb-girdle muscular dystrophies : clinical, genetic relative frequency in a large Italian population 28-giu-2007 M. GuglieriF. MagriR. CaglianiF. FortunatoS. LucchiariS. SalaniR. Del BoC. ZeccaC. LampertiN. BresolinG.P. Comi + Article (author) -
Autosomal dominant and recessive limb-girdle muscular dystrophies: relative frequency in a large Italian population 1-gen-2005 M.GuglieriF. MagriF. FortunatoS. LucchiariR. Del BoA. BordoniC. ZeccaC. LampertiN. BresolinG.P. Comi + Article (author) -
Autosomal Recessive Ala93Thr mutation in caveolin-3 gene : a new family 1-ott-2008 F.M.B. MagriC. LampertiD. RonchiE. FassoneN. BresolinG.P. Comi + Article (author) -
Autosomal recessive myopathy without inclusion bodies caused by GNE gene mutation. 1-gen-2006 R.DEL BOM. GUGLIERIF.MAGRIN. BRESOLING.P. COMI. + Article (author) -