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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 SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases Eur J Hum Genet 24:1016-1021, Choquet,K.,et al, 2016 Diseases of the Nervous System Caused by Nutritional Deficiency, Vitamin B12 (Cobalamin) Deficiency (Subacute Combined Degeneration) Adams & Victors Principles of Neurology Chp 41, pg 1172, Ropper, A.H.,et al, 2014 Primary Lateral Sclerosis, Clin Features, Neuropath & Dx Criteria Brain 115:495-520, Pringle,C.E.,et al, 1992 Neurologic Aspects of Cobalamin Deficiency Medicine 70:229-245, Healton,E.B.,et al, 1991 Primary Lateral Sclerosis, A Clinical Diagnosis Reemerges Arch Neurol 45:1304-1307, Younger,D.S.,et al, 1988 Hyperthyroidism Presenting as Pyramidal Tract Disease BMJ 297:1395-1396, Shaw,P.J.,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 Showing articles 0 to 9 of 9