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Showing articles 0 to 9 of 9 Filter Applied: pyramidal tract (Click to remove) Hallervorden-Spatz Syndrome and Brain Iron Metabolism Arch Neurol 48:1285-1293, Swaiman,K.F., 1991 Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases AJNR 39:1657-1661, Codjia, P.,et al, 2018 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 Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands Neurol 28:703, Coutinho,P.,et al, 1978 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 9 of 9