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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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Neuroimaging Features of Biotinidase Deficiency
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Pyruvate Dehydrogenase Deficiency (PDCD)
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Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
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Clinicopathologic Conference, Tay-Sacks Disease (GM2, Gangliosidosis)
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Inherited Metabolic Diseases of the Nervous System, Tay Sachs Disease
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Intracranial Optic Nerve Enlargement in Infantile Krabbe Disease
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Clinicopath Conf, Infantile Krabbe Disease
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Neurological Findings in Aminoacylase 1 Deficiency
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Aromatic L-Amino Acid Decarboxylase Deficiency
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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Hematopoietic Stem-Cell Transplantation in Globoid-Cell Leukodystrophy
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Neurologic Crises in Hereditary Tyrosinemia
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Cytochrome c Oxidase Deficiency in Leigh Syndrome
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Arch Neurol 35:475, Bosch,E.P., 1978
Possible Biochemical Basis of Memory Disorder in Alzheimer Disease
Ann Neurol 3:471, Smith,C.M.,et al, 1978
Adult-onset GM2 Gangliosidosis
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Neurological Manifestations of Fabry Disease in Female Carriers
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Specificity of the Urine Inhibitor Test for Leigh's Disease
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