IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

D'ANGELO, MARIA GRAZIA

D'ANGELO, MARIA GRAZIA  

Universita' degli Studi di MILANO  

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Titolo Data di pubblicazione Autori Tipo File Abstract
Abdominal volume contribution to tidal volume as an early indicator of respiratory impairment in Duchenne Muscular Dystrophy 1-gen-2010 M.G. D'AngeloG.P. ComiN. Bresolin + 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) -
Atypical adult onset complicated spastic paraparesis with thin corpus callosum in two patients carrying a novel FA2H mutation 1-gen-2012 TONELLI, ALESSANDRA EMMAM.G. D'AngeloF. ArrigoniE. BrighinaA. CitterioN. Bresolin + Article (author) -
Autonomy level and quality of everyday experience of people with Hereditary Spastic Paraplegia 1-set-2019 Sartori, Raffaela D. G.D'Angelo, Maria GraziaDelle Fave, Antonella + Article (author) -
Bioengineering and muscular dystrophy 1-gen-2009 M.G. D’AngeloS. GandossiniS. BonatoG.P. ComiN. Bresolin. + Conference Object -
Caratterizzazione clinica e molecolare della mutazione MERRF A8344G in una famiglia senza coinvolgimento del SNC 1-gen-2010 V. LucchiniD. RonchiM. G. D'AngeloA. BordoniL. PeverelliN. BresolinG.P. Comi + Conference Object -
Case Reports: Novel Missense Variants in the Filamin C Actin Binding Domain Cause Variable Phenotypes 1-gen-2022 D'Angelo, Maria GraziaNapoli, LauraCinnante, ClaudiaComi, Giacomo PietroRonchi, DarioBassi, Maria Teresa + Article (author) -
Clinical and genetic features of a cohort of patients with MFN2-related neuropathy 13-apr-2022 Abati E.Manini A.Del Bo R.Rizzo F.Bresolin N.Bellone E.Bassi M. T.D'Angelo M. G.Comi G. P.Corti S. + Article (author) -
Clinical and genetical variability in a large sample of LGMD Italian patients 1-gen-2007 F. MagriM. GuglieriM. D’AngeloR. CaglianiR. Del BoD. RonchiC. LampertiF. FortunatoN. BresolinG.P.Comi + Conference Object -
Clinical evaluation of muscular dystrophies: new tools from BioEngineering. 1-giu-2009 M.G. D’AngeloS. GandossiniS. BonatoG.P. ComiN. Bresolin + Conference Object -
Clinical trial using nitric oxide releasing drug and nonsteroidal antiinflammatory drugs in muscular dystrophy: Design of a study. 1-gen-2009 S. GandossiniM.G. d’AngeloS. BonatoG.P. ComiF. MagriN. BresolinE. Clementi + Conference Object -
De novo small duplication in Lamin A/C gene associated with congenital muscular dystrophy phenotype. 1-giu-2009 F. MagriR. Del BoC. LampertiM.G. D’AngeloG.P. Comi. + Conference Object -
Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase 1-giu-2020 Mauri E.Abati E.D'Angelo M. G.Lucchini M.Bello L.Benedetti L.Scarlato M.Bertini E.Politano L.Scutifero M.Fossati B.Sansone V.Gagliardi D.Costamagna G.Govoni A.Magri F.Brusa R.Meneri M.Corti S.Bresolin N.Nigro V.Antonini G.Comi G. P. + Article (author) -
Genetic modifiers of respiratory function in Duchenne muscular dystrophy 1-mag-2020 Bello L.D'Angelo G.Gandossini S.Magri F.Comi G. P.Sansone V. A. + Article (author) -
Genetic modifiers of upper limb function in Duchenne muscular dystrophy 1-gen-2022 D'Angelo, GraziaMagri, FrancescaComi, Giacomo PBruno, Claudio + Article (author) -
Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-up 1-set-2011 F. MagriA. GovoniM.G. D'AngeloR. Del BoA. BordoniTEDESCHI, SABRINAF. FortunatoV. LucchiniS. BonatoC. LampertiY. TorrenteS. CortiN. BresolinG.P. Comi + Article (author) -
Genotype and phenotype correlation in dysferlinopathies 1-gen-2007 F. MagriR. CaglianiM.G. D'AngeloR. Del BoF. FortunatoN. BresolinG.P. Comi + Conference Object -
In vitro and in vivo tetracycline-controlled myogenic conversion of NIH-3T3 cells : Evidence of programmed cell death after muscle cell transplantation 1-apr-2001 Y. TorrenteS. CortiM.G. D'AngeloG.P. ComiS. SalaniF. PisatiAUSENDA, CARLO DOMENICOG. ScarlatoN. Bresolin + Article (author) -
Incidental Mitochondrial Myopathy 1-gen-2010 V. CrugnolaV. LucchiniD. RonchiM.G. D'AngeloA. BordoniL. PeverelliN. BresolinG.P. Comi + Conference Object -
Intrafamilial variable presentation of CMT2, spastic paraparesis and cognitive impairment caused by a novel autosomal dominant MFN2 mutation 1-gen-2007 R. Del BoS. BonatoM.G. D’AngeloN. BresolinG.P. Comi + Conference Object -