BELLO, LUCA

BELLO, LUCA  

Dipartimento di Neuroscienze - DNS  

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Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
226thENMC International Workshop:. Towards validated and qualified biomarkers for therapy development for Duchenne muscular dystrophy 20-22 January 2017, Heemskerk, The Netherlands 2017 Bello, Luca + NEUROMUSCULAR DISORDERS - -
24 month longitudinal data in ambulant boys with duchenne muscular dystrophy. 2013 BELLO, LUCAPEGORARO, ELENA + PLOS ONE - -
6 minute walk test in Duchenne MD patients with different mutations: 12 month changes. 2014 BELLO, LUCAPEGORARO, ELENA + PLOS ONE - -
A Mutation in the CASQ1 Gene Causes a Vacuolar Myopathy with Accumulation of Sarcoplasmic Reticulum Protein Aggregates. 2014 TONIOLO, LUANAPEGORARO, ELENABELLO, LUCAREGGIANI, CARLO + HUMAN MUTATION - -
Ablation of collagen VI leads to the release of platelets with altered function 2021 Chrisam M.Semplicini C.Petronilli V.Bello L.Pegoraro E.Bernardi P.Braghetta P.Bonaldo P. + BLOOD ADVANCES - -
Age, corticosteroid treatment and site of mutations affect motor functional changes in young boys with Duchenne Muscular Dystrophy 2022 Bello, LucaPegoraro, Elena + PLOS ONE - -
Assessing Dysferlinopathy Patients Over Three Years With a New Motor Scale 2021 Bello L.Pegoraro E. + ANNALS OF NEUROLOGY - -
Assessing the Relationship of Patient Reported Outcome Measures With Functional Status in Dysferlinopathy: A Rasch Analysis Approach 2022 Bello L.Pegoraro E. + FRONTIERS IN NEUROLOGY - -
Assessment of disease progression in dysferlinopathy: A 1-year cohort study 2019 Bello L.Semplicini C.Pegoraro E. + NEUROLOGY - -
Assessment of patients with idiopathic inflammatory myopathies and isolated creatin-kinase elevation 2014 IACCARINO, LUCAPEGORARO, ELENABELLO, LUCASEMPLICINI, CLAUDIOSORARU', GIANNIGHIRARDELLO, ANNADORIA, ANDREA + AUTOIMMUNITY HIGHLIGHTS - -
Association Study of Exon Variants in the NF-κB and TGFβ Pathways Identifies CD40 as a Modifier of Duchenne Muscular Dystrophy 2016 BELLO, LUCABARP, ANDREAVIANELLO, SARAPEGORARO, ELENA + AMERICAN JOURNAL OF HUMAN GENETICS - -
Becker muscular dystrophy due to an intronic splicing mutation inducing a dual dystrophin transcript 2016 FANIN, MARINABELLO, LUCAPEGORARO, ELENA + NEUROMUSCULAR DISORDERS - -
Benefits of glucocorticoids in non-ambulant boys/men with Duchenne muscular dystrophy: A multicentric longitudinal study using the Performance of Upper Limb test 2015 PEGORARO, ELENABELLO, LUCABARP, ANDREA + NEUROMUSCULAR DISORDERS - -
Burden, professional support, and social network in families of children and young adults with muscular dystrophies 2014 ANGELINI, CORRADOGAIANI, ALESSANDRASEMPLICINI, CLAUDIOBELLO, LUCA + MUSCLE & NERVE - -
Cardiomyopathy in patients with POMT1-related congenital and limb-girdle muscular dystrophy. 2012 BELLO, LUCALeonardi ESORARU', GIANNIPALMIERI, ARIANNAVianello AAngelini CTOSATTO, SILVIOPEGORARO, ELENA + EUROPEAN JOURNAL OF HUMAN GENETICS - -
Cardiorespiratory management of Duchenne muscular dystrophy: emerging therapies, neuromuscular genetics, and new clinical challenges 2022 Bello L.Pegoraro E. + THE LANCET RESPIRATORY MEDICINE - -
Caregiver psychological profile and perceived quality of life in children affected by Duchenne Muscular Dystrophy 2013 BARP, ANDREAMARCATO, SONIAPALMIERI, ARIANNACALVO, VINCENZOKLEINBUB, JOHANN ROLANDBELLO, LUCAPEGORARO, ELENA AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION - -
Changes in Muscle Metabolism are Associated with Phenotypic Variability in Golden Retriever Muscular Dystrophy 2017 Bello, Luca + THE YALE JOURNAL OF BIOLOGY AND MEDICINE - -
Clinical and genetic spectrum in limb-girdle muscular dystrophy type 2E 2015 SEMPLICINI, CLAUDIOBELLO, LUCAANGELINI, CORRADOPEGORARO, ELENA + NEUROLOGY - -
Clinical and molecular characterization of limb girdle muscular dystrophy due to LAMA2 mutations. 2011 BELLO, LUCASORARU', GIANNIAngelini CPEGORARO, ELENA + MUSCLE & NERVE - -