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Showing articles 0 to 8 of 8 Filter Applied: pyramidal tract dysfunction (Click to remove) Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006 Clinicopath Conf Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992 SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases Eur J Hum Genet 24:1016-1021, Choquet,K.,et al, 2016 Multiple-System Atrophy NEJM 372:249-263, Fanciulli, A. & Wenning, G.K., 2015 Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Gertsmann-Straussler Schneinker Syndrome Adams & Victors Principles of Neurology, Chp 33, pg 773, Ropper, A.H.,et al, 2014 Degenerative Diseases of the Nervous System, Amyotrophic Lateral Sclerosis Adams & Victors Principles of Neurology, Chp 39, pg 1109, Ropper, A.H.,et al, 2014 The Acquired Immunodeficiency Syndrome (AIDS) Dementia Complex Ann Int Med 111:400-410, Ho,D.D.,et al, 1989 Chronic Meningitis Medicine 55:341, Ellner,J.J.,et al, 1976 Showing articles 0 to 8 of 8