SEMPLICINI, CLAUDIO

SEMPLICINI, CLAUDIO  

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Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
1st International Workshop on Clinical trial readiness for sarcoglycanopathies 15-16 November 2016, Evry, France 2017 PEGORARO, ELENAGORECKI, DARIUSZ , CEZARYSANDONA', DORIANNASEMPLICINI, CLAUDIO + NEUROMUSCULAR DISORDERS - -
233rd ENMC International Workshop:: Clinical Trial Readiness for Calpainopathies, Naarden, The Netherlands, 15–17 September 2017 2018 EYMARD, BRUNO, MICHEL, ANTOINE, JOSEPH, MARIESemplicini C + NEUROMUSCULAR DISORDERS - -
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 - -
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 - -
Burden, professional support, and social network in families of children and young adults with muscular dystrophies 2014 ANGELINI, CORRADOGAIANI, ALESSANDRASEMPLICINI, CLAUDIOBELLO, LUCA + MUSCLE & NERVE - -
Clinical and genetic spectrum in limb-girdle muscular dystrophy type 2E 2015 SEMPLICINI, CLAUDIOBELLO, LUCAANGELINI, CORRADOPEGORARO, ELENA + NEUROLOGY - -
Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations 2016 CAO, MICHELANGELODONA', MARTASEMPLICINI, CLAUDIOCASSINA, MATTEOSORARU', GIANNISTRAMARE, ROBERTOSALVIATI, LEONARDOPEGORARO, ELENA + NEUROGENETICS - -
Clinical follow-up and efficacy evaluation in ERT 2012 ANGELINI, CORRADOSEMPLICINI, CLAUDIOPEGORARO, ELENA - - Advances in diagnosis and management of glycogenosis II
Clinical Scales for the Evaluation of Neuromuscular Patients 2013 SEMPLICINI, CLAUDIOANGELINI, CORRADO - - Muscular Dystrophy: Causes and Management
Effect of enzyme replacement therapy with alglucosidase alfa (Myozyme®) in 12 patients with advanced late-onset Pompe disease 2017 SEMPLICINI, CLAUDIO + MOLECULAR GENETICS AND METABOLISM - -
EMG diagnosis of McArdle disease with long exercise test 2016 SEMPLICINI, CLAUDIO + NEUROMUSCULAR DISORDERS - -
Enzyme Replacement Therapy for Pompe Disease 2011 ANGELINI, CORRADOSEMPLICINI, CLAUDIO CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS - -
Enzyme replacement therapy improves respiratory outcomes in patients with late-onset type II glycogenosis and high ventilator dependency 2013 Vianello ASEMPLICINI, CLAUDIOAngelini CPEGORARO, ELENA + LUNG - -
Enzyme Replacement Therapy in Juvenile and Adult Late-Onset Glycogenosis Type II 2011 SEMPLICINI, CLAUDIO CLINICAL THERAPEUTICS - -
Functional changes in Becker muscular dystrophy: Implications for clinical trials in dystrophinopathies 2016 BELLO, LUCABARP, ANDREAFANIN, MARINASEMPLICINI, CLAUDIOSORARU', GIANNIAngelini, CorradoPEGORARO, ELENA + SCIENTIFIC REPORTS - -
Genetic modifiers of Duchenne muscular dystrophy and dilated cardiomyopathy 2015 BARP, ANDREABELLO, LUCAMELACINI, PAOLACALORE, CHIARAPOLO, ANGELAVIANELLO, SARASORARU', GIANNISEMPLICINI, CLAUDIOPANTIC, BORISERMANI, MARIOCALVO, VINCENZOANGELINI, CORRADOPEGORARO, ELENA + PLOS ONE - -
High intra-familiar clinical variability in MORC2 mutated CMT2 patients 2017 SEMPLICINI, CLAUDIO + BRAIN - -
I-4 Long-term follow-up effects on enzyme replacement treatment of adult form of acid maltase deficiency myopathy 2011 ANGELINI, CORRADOSEMPLICINI, CLAUDIOPEGORARO, ELENA + ACTA MYOLOGICA - -
Integrated care of muscular dystrophies in Italy. Part 1. Pharmacological treatment and rehabilitative interventions 2017 Gaiani, AlessandraSemplicini, ClaudioBello, LucaAngelini, Corrado + ACTA MYOLOGICA - -