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Journal of Neuromuscular Diseases|July 6, 2020
Severe inflammatory myopathy in a pulmonary carcinoma patient treated with Pembrolizumab: An alert for myologistsL Peverelli, A De Rosa, E Domina, et al.Human Mutation|September 5, 2003
Mutational analysis of the AGL gene: five novel mutations in GSD III patientsS Lucchiari, M A Donati, D Melis, et al.Journal of Child Neurology|August 21, 2001
Leigh disease: clinical, neuroradiologic, and biochemical study of three new cases with cytochrome c oxidase deficiencyS Savasta, G P Comi, M P Perini, et al.Genes and Immunity|August 14, 2009
A population genetics study of the familial Mediterranean fever gene: evidence of balancing selection under an overdominance regimeM Fumagalli, R Cagliani, U Pozzoli, et al.Perceptual and Motor Skills|June 15, 2007
Language disturbances in a group of participants suffering from Duchenne muscular dystrophy: a pilot studyF Fabbro, A Marini, G Felisari, et al.Journal of the Neurological Sciences|June 20, 2001
Transcriptional activation of the non-muscle, full-length dystrophin isoforms in Duchenne muscular dystrophy skeletal muscleM Sironi, A Bardoni, G Felisari, et al.Human Mutation|November 21, 2002
Molecular characterisation of GSD III subjects and identification of six novel mutations in AGLS Lucchiari, M A Donati, R Parini, et al.Journal of Neurology|February 1, 1995
Ryanodine receptor gene point mutation and malignant hyperthermia susceptibilityI Moroni, E F Gonano, G P Comi, et al.Neuromuscular Disorders : NMD|January 1, 1992
Congenital myopathy associated with abnormal accumulation of desmin and dystrophinA Prelle, M Moggio, G P Comi, et al.Journal of the Neurological Sciences|January 1, 1997
The apolipoprotein E epsilon4 allele causes a faster decline of cognitive performances in Down's syndrome subjectsR Del Bo, G P Comi, N Bresolin, et al.Pageof 10