Beyond exome-targeted sequencing approaches to increase the diagnostic rate of unsolved neuromuscular disease patients

Severe epileptic encephalopathy with progressive cerebral and cerebellar atrophy and peripheral neuropathy: a new GEMIN5 phenotype?

Clinical features in a large cohort of adults with Duchenne muscular dystrophy treated with glucocorticoids

Clinical characterization of a large monocentre cohort of patients with Becker Muscular Dystrophy

Primary and Secondary Results of LUMINESCE, a Phase 3 Study of Interleukin-6 Signalling Inhibition by Satralizumab in Generalized Myasthenia Gravis

AChR-Seropositive Myasthenia Gravis in Muscular Dystrophy: diagnostic pitfalls and clinical management challenges