Carmelo Rodolico

Clinical, molecular, and protein correlations in a large sample of genetically diagnosed Italian limb girdle muscular dystrophy patients

Michela Guglieri, Francesca Magri, Maria Grazia D’Angelo et al. · Human Mutation · 2007 · 208 citations

Genetics, Genetic Epidemiology, Pathology +18

Hexosamine Biosynthetic Pathway Mutations Cause Neuromuscular Transmission Defect

Jan Senderek, Juliane Müller, Marina Dusl et al. · The American Journal of Human Genetics · 2011 · 171 citations · Full text

Neuromuscular Junction, Molecular Neuroscience, Medicine +6

A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score

Costanza Lamperti, Greta Fabbri, Liliana Vercelli et al. · Muscle & Nerve · 2010 · 151 citations · Full text

Muscle Function, Diagnosis, Orthopaedic Surgery +17

Phenotypic clustering of lamin A/C mutations in neuromuscular patients

Sara Benedetti, I. Menditto, Massimo Degano et al. · Neurology · 2007 · 128 citations

Safety and efficacy of intravenous bimagrumab in inclusion body myositis (RESILIENT): a randomised, double-blind, placebo-controlled phase 2b trial

Michael G. Hanna, Umesh A. Badrising, Olivier Benvéniste et al. · The Lancet Neurology · 2019 · 128 citations · Full text

Autoimmune Disease, Immunology, Placebo-controlled Phase 2B +4