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Auto- Immunity Highlights|May 23, 2015
Assessment of patients with idiopathic inflammatory myopathies and isolated creatin-kinase elevationL Iaccarino, E Pegoraro, L Bello, et al.Neuroepidemiology|January 1, 1993
Reappraisal of the incidence rate of Duchenne and Becker muscular dystrophies on the basis of molecular diagnosisM L Mostacciuolo, M Miorin, E Pegoraro, et al.La Radiologia Medica|February 24, 2010
MRI in the assessment of muscular pathology: a comparison between limb-girdle muscular dystrophies, hyaline body myopathies and myotonic dystrophiesR Stramare, V Beltrame, R Dal Borgo, et al.Neurology|October 1, 1996
Myotonia and the muscle chloride channel: dominant mutations show variable penetrance and founder effectP P Koty, E Pegoraro, G Hobson, et al.Scientific Reports|September 13, 2018
Unimpaired Neuropsychological Performance and Enhanced Memory Recall in Patients with Sbma: A Large Sample Comparative StudyS Marcato, J R Kleinbub, G Querin, et al.Acta Neurologica Scandinavica|May 18, 2013
No evidence of cardiomyopathy in spinal and bulbar muscular atrophyG Querin, P Melacini, C D'Ascenzo, et al.Journal of the Neurological Sciences|October 1, 1996
Prognostic factors in mild dystrophinopathiesC Angelini, M Fanin, M P Freda, et al.Neuromuscular Disorders : NMD|March 27, 1999
Cardiac transplantation in a Duchenne muscular dystrophy carrierP Melacini, M Fanin, A Angelini, et al.European Journal of Neurology|June 27, 2013
A novel SACS mutation results in non-ataxic spastic paraplegia and peripheral neuropathyE Gregianin, G Vazza, E Scaramel, et al.Annals of Neurology|November 1, 1996
Congenital muscular dystrophy with primary laminin alpha2 (merosin) deficiency presenting as inflammatory myopathyE Pegoraro, P Mancias, S H Swerdlow, et al.Pageof 8