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Showing articles 0 to 6 of 6 Filter Applied: pyramidal tract (Click to remove) SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases Eur J Hum Genet 24:1016-1021, Choquet,K.,et al, 2016 Adult-Onset Krabbe Disease with Mutation in the Galactocerebrosidase Gene, MRI of Corticospinal Tract Demyelin Neurol 49:1392-1399, Satoh,J.-I.,et al, 1997 Cognitive and Brain Magnetic Resonance Imaging Findings in Adrenomyeloneuropathy Ann Neurol 40:675-678, Edwin,D.,et al, 1996 Primary Lateral Sclerosis, A Clinical Diagnosis Reemerges Arch Neurol 45:1304-1307, Younger,D.S.,et al, 1988 Reversible Corticospinal Tract Disease Due to Hyperthyrodisim Arch Neurol 34:647, Garcia,C.A.,et al, 1977 Clinical Pathological Conference, Scleroderma, Spastic Paraparesis & Chronic Myelogenous Leukemia Prov. VAH, Dec. 12, 77., Finelli,P.F., 1850 Showing articles 0 to 6 of 6