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Peripheral Neuropathy in Amyotrophic Chorea-Acanthocytosis
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A pedigree of Amyotrophic Chorea With Acantho-cytosis
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Familial Degeneration of the Basal Ganglia with Acanthocytosis:a Clinical Neuropathological, & Neurochemical Study
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Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
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Movement Disorders in Patients with Genetic Developmental and Epileptic Encephalopathies
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A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
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Neurodegeneration with Brain Iron Accumulation
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A 13-year-old boy with Chronic Ataxia and Developmental Delay
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A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
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Huntington Disease: Clinical Features and Diagnosis
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Choreoathetosis, Dystonia, and Myoclonus in 3 Siblings with Autosomal Recessive Spinocerebellar Ataxia Type 16
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Infantile Bilateral Striatal Necrosis Maps to Chromosome 19q
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Familial Infantile Bilateral Striatal Necrosis
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Niemann-Pick Disease Type C: Two Cases and an Update
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Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
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The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
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Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
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The Prevention of Neurogenetic Disease
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Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
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A Worldwide Study of the Huntington's Disease Mutation, The Sensitivity & Specificity of Measuring CAG Repeats
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Trinucleotide Repeat Expansion in Neurological Disease
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Clinical Consequences of Isolating the Gene for Huntington's Disease
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Acute Profound Dystonia in Infants with Glutaric Acidemia
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Problems in Genetic Prediction for Huntington's Disease
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Uptake of Presymptomatic Predictive Testing for Huntington's Disease
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Predictive Testing for Huntington's Disease with Use of a Linked DNA Marker
NEJM 318:535-542, Meissen,G.J.,et al, 1988
The Molecular Genetic Revolution, Its Impact on Clinical Neurology
Arch Neurol 45:1366-1376, Payne,C.S.&Roses,A.D., 1988
Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
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Genetic Linkage in Neurologic Diseases
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The Combined Use of Positron Emission Tomography & DNA Polymorphisms for Preclinical Detection of Huntington's Disease
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Neurological Manifestations in Xeroderma Pigmentosum
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Infantile Bilateral Striatal Necrosis, Clinicopathological Classification
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Olivopontocerebellar Atrophy with Dementia, Blindness, & Chorea, Response to Baclofen
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Parental Transmission in Huntington's Disease
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Genetic Testing in Huntington's Disease
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Huntington's Chorea:Neglected Opportunities for Preventive Medicine
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Biochemical Evidence Of Dysfunction Of Brain Neurotransmitters In The Lesch-Nyhan Syndrome
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Abetalipoproteinemia, Report of Two Cases & Review of Therapy
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Huntington's Disease:Abnormality of Lymphocyte Capping
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Familial Inverted Choreoathetosis
Neurol 29:1627-1631, Fisher,M.,et al, 1979
Diagnosis of Treatable Wilson's Disease
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Familial Chorea & Myoclonus Epilepsy
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