LGMD phenotype due to a new gene and dysferlinopathy investigated by next-generation sequencing

Por Angelini, Corrado I.
Publicado no Neurol Genet (2015)

Old and new therapeutic developments in steroid treatment in Duchenne muscular dystrophy

Por ANGELINI, CORRADO, PETERLE, ENRICO
Publicado em 2012

Fatigue in muscular dystrophies

Por Angelini, Corrado, Tasca, Elisabetta
Publicado em 2012

Diagnosis by protein analysis of dysferlinopathy in two patients mistaken as polymyositis

Por Angelini, Corrado, Grisold, Wolfgang, Nigro, Vincenzo
Publicado em 2011

New treatments for myasthenia: a focus on antisense oligonucleotides

Por Angelini, Corrado, Martignago, Sara, Bisciglia, Michela
Publicado em 2013

Therapeutic advances in the management of Pompe disease and other metabolic myopathies

Por Angelini, Corrado, Nascimbeni, Anna Chiara, Semplicini, Claudio
Publicado em 2013

Autonomic regulation in muscular dystrophy

Por Angelini, Corrado, Di Leo, Rita, Cudia, Paola
Publicado em 2013

Autophagy in Natural History and After ERT in Glycogenosis Type II

Por Angelini, Corrado, Nascimbeni, Anna C., Fanin, Marina
Publicado no JIMD Rep (2015)

How to tackle the diagnosis of limb-girdle muscular dystrophy 2A

Por Fanin, Marina, Nascimbeni, Anna Chiara, Tasca, Elisabetta, Angelini, Corrado
Publicado em 2009

Transcriptional and Translational Effects of Intronic CAPN3 Gene Mutations

Por Nascimbeni, Anna Chiara, Fanin, Marina, Tasca, Elisabetta, Angelini, Corrado
Publicado em 2010

Muscle fatigue, nNOS and muscle fiber atrophy in limb girdle muscular dystrophy

Por ANGELINI, CORRADO, TASCA, ELISABETTA, NASCIMBENI, ANNA CHIARA, FANIN, MARINA
Publicado no Acta Myol (2014)

Lipolysis and lipophagy in lipid storage myopathies

Por Angelini, Corrado, Nascimbeni, Anna Chiara, Cenacchi, Giovanna, Tasca, Elisabetta
Publicado no Biochim Biophys Acta (2016)

Autophagy dysregulation in Danon disease

Por Nascimbeni, Anna Chiara, Fanin, Marina, Angelini, Corrado, Sandri, Marco
Publicado no Cell Death Dis (2017)

Inhibition of muscle fibrosis results in increases in both utrophin levels and the number of revertant myofibers in Duchenne muscular dystrophy

Por Levi, Oshrat, Genin, Olga, Angelini, Corrado, Halevy, Orna, Pines, Mark
Publicado no Oncotarget (2015)

GYG1 gene mutations in a family with polyglucosan body myopathy

Por Fanin, Marina, Torella, Annalaura, Savarese, Marco, Nigro, Vincenzo, Angelini, Corrado
Publicado no Neurol Genet (2015)

Impaired autophagy contributes to muscle atrophy in glycogen storage disease type II patients

Por Nascimbeni, Anna Chiara, Fanin, Marina, Masiero, Eva, Angelini, Corrado, Sandri, Marco
Publicado em 2012

S2.1 Enzyme replacement therapy (ERT) in Glycogen Storage Disease Type II: the first treatment developed

Por Angelini, Corrado, Semplicini, Claudio, Fanin, Marina, Nascimbeni, Annachiara, Peterle, Enrico, Pegoraro, Elena
Publicado em 2011

Muscle exercise in limb girdle muscular dystrophies: pitfall and advantages

Por SICILIANO, GABRIELE, SIMONCINI, COSTANZA, GIANNOTTI, STEFANO, ZAMPA, VIRNA, ANGELINI, CORRADO, RICCI, GIULIA
Publicado no Acta Myol (2015)

Identification of an intragenic deletion in the SGCB gene through a re-evaluation of negative next generation sequencing results

Por Giugliano, Teresa, Fanin, Marina, Savarese, Marco, Piluso, Giulio, Angelini, Corrado, Nigro, Vincenzo
Publicado no Neuromuscul Disord (2016)

Generalized Lysosome-Associated Membrane Protein-2 Defect Explains Multisystem Clinical Involvement and Allows Leukocyte Diagnostic Screening in Danon Disease

Por Fanin, Marina, Nascimbeni, Anna C., Fulizio, Luigi, Spinazzi, Marco, Melacini, Paola, Angelini, Corrado
Publicado em 2006