Showing results (61-70 of 599) with videos related to
Sort By:
Pageof 60
Neuromuscular Disorders : NMD|July 19, 2000
Clinico-electrophysiological correlation of extensor digitorum brevis muscle atrophy in children with charcot-marie-tooth disease 1A duplicationJ Berciano, A García, J Calleja, et al.Journal of Neurology, Neurosurgery, and Psychiatry|February 1, 1993
Hereditary "pure" spastic paraplegia: a study of nine familiesJ M Polo, J Calleja, O Combarros, et al.Neurologia|February 9, 2016
Why do motor neurons degenerate? Actualization in the pathogenesis of amyotrophic lateral sclerosisJ Riancho, I Gonzalo, M Ruiz-Soto, et al.Neurologia (Barcelona, Spain)|December 18, 2010
Multimodal neurophysiological study of SCA2 and SCA3 autosomal dominant hereditary spinocerebellar ataxiasS Álvarez-Paradelo, A García, J Infante, et al.Surgical Neurology|May 1, 1989
Congenital giant pigmented nevus and intracranial arteriovenous malformationC Leno, M J Sedano, O Combarros, et al.Acta Neurologica Scandinavica|April 1, 1994
Guillain-Barré syndrome in Cantabria, Spain. An epidemiological and clinical studyM J Sedano, J Calleja, E Canga, et al.Brain : a Journal of Neurology|April 1, 1991
Hereditary ataxias and paraplegias in Cantabria, Spain. An epidemiological and clinical studyJ M Polo, J Calleja, O Combarros, et al.Acta Neurologica Scandinavica|January 1, 1987
Prevalence of hereditary motor and sensory neuropathy in CantabriaO Combarros, J Calleja, J M Polo, et al.Neurologia (Barcelona, Spain)|May 20, 2004
[Influence of botulinum toxin treatment on previous primary headaches in patients with cranio-cervical dystonia]J PascualPageof 60