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Neuromuscular Disorders : NMD|June 3, 2008
POMT1 and POMT2 mutations in CMD patients: a multicentric Italian studyS Messina, M Mora, E Pegoraro, et al.Journal of Neurology|July 12, 2017
Revisiting mitochondrial ocular myopathies: a study from the Italian NetworkD Orsucci, C Angelini, E Bertini, et al.Neurology|July 8, 2011
Functional changes in Duchenne muscular dystrophy: a 12-month longitudinal cohort studyE Mazzone, G Vasco, M P Sormani, et al.Neurology|March 21, 2009
Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population studyE Mercuri, S Messina, C Bruno, et al.Orphanet Journal of Rare Diseases|July 9, 2016
MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patientsC Fiorillo, G Astrea, M Savarese, et al.Neuromuscular Disorders : NMD|June 26, 2009
Reliability of the North Star Ambulatory Assessment in a multicentric settingE S Mazzone, S Messina, G Vasco, et al.Pageof 8