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Journal of the Neurological Sciences|October 1, 1983
Dominantly inherited motor and sensory neuropathy type I. Genetic, clinical, electrophysiological and pathological features in four familiesO Combarros, J Calleja, J Figols, et al.Neurology|June 1, 1996
Cough, exertional, and sexual headaches: an analysis of 72 benign and symptomatic casesJ Pascual, F Iglesias, A Oterino, et al.Brain : a Journal of Neurology|December 1, 1983
Livedo reticularis and cerebrovascular lesions (Sneddon's syndrome). Clinical, radiological and pathological features in eight casesM Rebollo, J F Val, F Garijo, et al.Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1982
Familial cerebellar ataxia and hypogonadotropic hypogonadism: evidence for hypothalamic LHRH deficiencyJ Berciano, J A Amado, J Freijanes, et al.Neurologia (Barcelona, Spain)|May 3, 2001
[Neurologic complications of herpes zoster. A retrospective study in 100 patients]M Sánchez-Guerra, J Infante, J Pascual, et al.Brain Research|February 8, 2000
Loss of dopamine uptake sites and dopamine D2 receptors in striatonigral degenerationA M González, J Berciano, J Figols, et al.Neurophysiologie Clinique = Clinical Neurophysiology|July 30, 2008
Acute motor conduction block neuropathy pattern occurring in the course of an acute inflammatory demyelinating polyradiculoneuropathyJ L Fernández-Torre, J Berciano, I García-Gorostiaga, et al.Revista De Neurologia|July 23, 1998
[Miller-Fisher syndrome: electrophysiological serial study of five patients]J Calleja, A García, C de Pablos, et al.Journal of Virology|August 1, 1995
Replication of hepatitis delta virus RNA in mice after intramuscular injection of plasmid DNAJ M Polo, B Lim, S Govindarajan, et al.Acta Neurologica Scandinavica|December 5, 2003
Expanded GAA repeats and clinical variation in Friedreich's ataxiaI Mateo, J Llorca, V Volpini, et al.Pageof 19