Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
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Postoperative Neurologic Complications after Open Heart Surgery on Young Infants
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The Prevention of Neurogenetic Disease
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Juvenile Huntington Disease:CT and MR Features
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Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
Neurol 45:1739-1743, Shulman,L.M.,et al, 1995
Postvaricella Basal Ganglia Infarction in Children
AJNR 16:449-452, Silverstein,F.S.&Brunberg,J.A., 1995
Hereditary Late-Onset Chorea Without Significant Dementia:Genetic Evid for Phenotypic Variation in Huntington's Disease
Neurol 45:443-447, Britton,J.W.,et al, 1995
Hemiballismus in Systemic Lupus Erythematosus: Possible Association with Antiphospholipid Antibodies
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Trinucleotide Repeat Expansion in Neurological Disease
Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994
Prothrombotic States in Young People with Idiopathic Stroke:Prospective Study
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Rheumatic Heart Disease and Sneddon's Syndrome
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Pseudochoreoatheotosis:Movement Associated with Loss of Proprioception
Arch Neurol 51:1103-1109, Sharp,F.R.,et al, 1994
Cortical Myoclonus in Huntington's Disease
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Movement Disorders Following Lesions of the Thalamus or Subthalamic Region
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Cerebral Involvement in McLeod Syndrome
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Speculations on Antineuronal Antibody-Mediated Neuropsychiatric Disorders of Childhood
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Cocaine-Induced Choreoathetoid Movements ('Crack Dancing')
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The Neurogenetic Genie:Testing for Huntington's Disease Mutation
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CAG Repeat Size and Clinical Presentation in Huntington's Disease
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A Worldwide Study of the Huntington's Disease Mutation, The Sensitivity & Specificity of Measuring CAG Repeats
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Clozapine in Huntington's Chorea
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Choreoathetosis after Surgery for Congenital Heart Disease
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Methylmercury Poisoning:Long-Term Clinical, Radiological, Toxicological, and Pathological Studies of an Affected Family
Ann Neurol 35:680-688, Davis,L.E.,et al, 1994
Reduced Basal Ganglia Volume Associated with the Gene for Huntington's Disease in Asymptomatic at-Risk Persons
Neurol 44:823-828, Aylward,E.H.,et al, 1994
Choreiform Movements Associated with the Use of Valproate
Arch Neurol 51:702-704, Lancman,M.E.,et al, 1994
Trinucleotide Repeat Length and Rate of Progression of Huntington's Disease
Ann Neurol 36:630-635, Illarioshkin,S.N.,et al, 1994
Mutation Analysis in Patients with Possible but Apparently Sporadic Huntington's Disease
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A 10-Year Experience with Postpump Chorea
Ann Neurol 34:820-826, Medlock,M.D.,et al, 1993
Molecular Genetics in Neurology
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The Polymerase Chain Reaction:Application to Nervous System Disease
Ann Neurol 34:513-523, Darnell,R.B., 1993
An Unusual Cause of Cerebral Venous Thrombosis in a Four-Year-Old Child
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Clinical Consequences of Isolating the Gene for Huntington's Disease
BMJ 307:397-398, Harper,P.S., 1993
Tardive Stereotype and Other Movement Disorders in Tardive Dyskinesias
Neurol 43:937-941, Stacy,M.,et al, 1993
Sydenham's Chorea:Physical and Psychological Symptoms of St. Vitus Dance
Pediatrics 91:706-713, Swedo,S.E.,et al, 1993
Alternating Hemiplegia of Childhood
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Ischemic Stroke Due to Deficiency of Coagulation Inhibitors, Report of 10 Young Adults
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Free Protein S Deficiency in Acute Ischemic Stroke, A Case-Control Study
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Clinical and Magnetic Resonance Features of the Classic & Akinetic-Rigid Variants of Huntington's Dis
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Movement Disorders with Cerebral Toxoplasmosis and AIDS
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Alternating Hemiplegia of Childhood:A Study of 10 Pts & Results of Flunarizine Treatment
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Attitudes Toward Direct Predictive Testing for the Huntington Disease Gene
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Serial Changes of Cerebral Glucose Metab & Caudate Size in Persons at Risk for Huntington's Dis
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Movement Disorders in Astrocytomas of the Basal Ganglia and the Thalamus
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A Synd of Autosomal Dominant Alternating Hemiplegia:Mimicking Intractable Epilepsy; Chromosomal Studies; Physiol Investig
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The Psychological Consequences of Predictive Testing for Huntington's Disease
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Long-Term Neurologic Consequences of Nutritional Vitamin B12 Deficiency in Infants
J Pediatr 121:710-714, Graham,S.M.,et al, 1992
Putamen Volume Reduction on Magnetic Resonance Imaging Exceeds Caudate Changes in Mild Huntington's Disease
Ann Neurol 31:69-75, Harris,G.J.,et al, 1992
Protein S Deficiency in Middle-Aged Women with Stroke
Neurol 42:1029-1033, Green,D.,et al, 1992
Postural Stability in Patients with Huntington's Disease
Neurol 42:1232-1238, Tian,J.,et al, 1992
Presymptomatic Testing for Huntington's Disease in the United Kingdom
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