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The Syndrome of Cutaneous Photosensitivity, Growth Failure, and Basal Ganglia Calcification
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A 23-Year-Old Man With Seizures and Visual Deficit
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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Mitochondrial DNA and Disease
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Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
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Acquired Ocular Visual Impairment in Children, 1960-1989
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Cockayne Syndrome: Review of 140 Cases
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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A Familial Syndrome of Dystonia, Blepharospasm, and Pigmentary Retinopathy
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Olivopontocerebellar Atrophy with Dementia, Blindness, & Chorea, Response to Baclofen
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Small Bowel Resection with Vitamin E Deficiency & Progressive Spinocerebellar Syndrome
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Phytanic Acid Storage Disease:Hearing Maintained After 15 Years of Dietary Treatment
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Heredopathia Atactica Polyneuritiformis
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Progressive Bulbar Paralysis Associated With Neurgl Deafness, A Nosological Entity
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Abetalipoproteinemia, Report of Two Cases & Review of Therapy
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Clinical & Extraneural Histologic Diagnosis of Neuronal Ceroidlipofuscinosis
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Kearns-Sayre Syndrome & Hypoparathyroidism
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A 28-Year-Old Woman with Vision Loss and an Unusual Gait
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A Clinical Triad to Diagnose Paraneoplastic Retinopathy
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A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy
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Paraneoplastic Syndromes Involving the Eyes
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The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture
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Optic-Nerve Degeneration in Alzheimer's Disease
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Congenital Hydrocephalus & Eye Abnormalities with Severe Developmental Brain Defects:Warburg's Syndrome
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Santavuori Disease:Diagnosis by Leukocyte Ultrastructure
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