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 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 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 -
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) -
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 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) -
Becker muscular dystrophy with a stop codon mutation in the 5′ of the dystrophin gene 1-ott-2008 F. MagriR. Del BoF. FortunatoR. CaglianiM. SironiV. CrugnolaN. BresolinG.P. Comi + Article (author) -
Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect. A Case Report and a Review of the Literature 2-ago-2018 Gagliardi, DeliaFaravelli, IreneVilla, LuisaCinnante, ClaudiaBrusa, RobertaMauri, EleonoraTresoldi, LauraMagri, FrancescaGovoni, AlessandraBresolin, NereoComi, Giacomo PCorti, Stefania + Article (author) -
CACNA1S mutation associated with a case of juvenile-onset congenital myopathy 1-gen-2021 Mauri E.Pagliarani S.Magri F.Manini A.Ripolone M.Borellini L.Cinnante C.Corti S.Bresolin N.Comi G. P. + Article (author) -
Can Intestinal Pseudo-Obstruction Drive Recurrent Stroke-Like Episodes in Late-Onset MELAS Syndrome? A Case Report and Review of the Literature 31-gen-2019 Gagliardi, DeliaMauri, EleonoraMagri, FrancescaMeneri, MegiAbati, ElenaBrusa, RobertaFaravelli, IreneRonchi, DarioTriulzi, FabioPeverelli, LorenzoBresolin, NereoComi, Giacomo PietroCorti, StefaniaGovoni, Alessandra + Article (author) -
Caratterizzazione molecolare dei geni CLCN1, SCN4A, KCNJ2, CACNA1S in pazienti con canalopatie muscolari 1-gen-2008 S. PagliaraniS. LucchiariS. CortiF. MagriM. CarpoN. BresolinG.P. Comi + Article (author) -
Cardiac and Neuromuscular Features of Patients with LMNA-Related Cardiomyopathy 1-ott-2019 Maggi, LorenzoMagri, FrancescaComi, Giacomo PBenedetti, Sara + Article (author) -
Central nervous system involvement in common variable immunodeficiency: A case of acute unilateral optic neuritis in a 26 -year-old Italian Patient 30-nov-2018 ABATI, ELENAFaravelli, IreneMagri, FrancescaGovoni, AlessandraGagliardi, DeliaMauri, EleonoraBrusa, RobertaBresolin, NereoFabio, GiovannaComi, Giacomo PietroCARRABBA, MARIA DOMENICA ROSARIACorti, Stefania + Article (author) -