MAGRI, FRANCESCA MARIA BENEDETTA

MAGRI, FRANCESCA MARIA BENEDETTA  

Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti  

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Risultati 1 - 20 di 152 (tempo di esecuzione: 0.018 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
24 month longitudinal data in ambulant boys with Duchenne muscular dystrophy 2013 Y. TorrenteF. MagriG.P. Comi + Article (author) -
6 minute walk test in duchenne MD patients with different mutations : 12 month changes 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 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 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 2010 F. MagriA. GovoniR. Del BoN. BresolinG.P. ComiS. Corti + Conference Object -
A novel GENE mutations causes familial recessive myopathy without inclusion bodies 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 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 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 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 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 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 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. 2008 D. RonchiA. BordoniE. FassoneF. MagriG.P. ComiM. Nizzardo + Conference Object -
Anti-sulfatide reactivity in patients with celiac disease 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 2022 Magri, FrancescaSalani, SabrinaFortunato, FrancescoMaggi, LorenzoCorti, StefaniaBresolin, NereoComi, Giacomo PietroRonchi, Dario + Article (author) -
Antisense Oligonucleotide Therapy for the Treatment of C9ORF72 ALS/FTD Diseases 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 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 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 2008 F.M.B. MagriC. LampertiD. RonchiE. FassoneN. BresolinG.P. Comi + Article (author) -
Autosomal recessive myopathy without inclusion bodies caused by GNE gene mutation. 2006 R.DEL BOM. GUGLIERIF.MAGRIN. BRESOLING.P. COMI. + Article (author) -