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Journal of Inherited Metabolic Disease|January 1, 1989
An unusual aminoacidopathy associated with mitochondrial encephalomyopathyT L Perry, S Hansen, F A Booth, et al.Neurology|February 1, 1984
Neurochemical abnormalities in a patient with ataxia-telangiectasiaT L Perry, S J Kish, D Hinton, et al.Journal of the Neurological Sciences|April 1, 1987
Tissue culture evidence for a circulating neurotoxin in Huntington's choreaT L Perry, V W Yong, S Hansen, et al.Neurology|July 1, 1980
Failure of aminooxyacetic acid therapy in Huntington diseaseT L Perry, J M Wright, S Hansen, et al.Canadian Medical Association Journal|June 21, 1975
Antibiotic abuse: the testimony of medical studentsT L PerryClinica Chimica Acta; International Journal of Clinical Chemistry|November 25, 1981
Mild elevations of plasma ornithine in homocystinuriaT L PerryNeuroscience Letters|January 22, 1982
Normal cerebrospinal fluid and brain glutamate levels in schizophrenia do not support the hypothesis of glutamatergic neuronal dysfunctionT L PerryJournal of the Neurological Sciences|October 1, 1989
Dominantly inherited olivopontocerebellar atrophy from eastern Cuba. Clinical, neuropathological, and biochemical findingsG Orozco, R Estrada, T L Perry, et al.Journal of the Neurological Sciences|November 1, 1987
Alpha-tocopherol and beta-carotene do not protect marmosets against the dopaminergic neurotoxicity of N-methyl-4-phenyl-1,2,3,6-tetrahydropyridineT L Perry, V W Yong, S Hansen, et al.Annals of Neurology|October 1, 1985
Hallervorden-Spatz disease: cysteine accumulation and cysteine dioxygenase deficiency in the globus pallidusT L Perry, M G Norman, V W Yong, et al.Pageof 228