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Risk of Neural Tube Defect-Affected Pregnancies Among Obese Women
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Hereditary Spastic Paraplegia:Advances in Genetic Research
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Intelligence and the X Chromosome
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The Epilepsy of Trisomy 9p
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X-Linked Malformation of Neuronal Migration
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Practice Parameter:The Neurodiagnostic Evaluation of the Child with First Simple Febrile Seizure
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Familial Temporal Lobe Epilepsy:A Common Disorder Identified in Twins
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Amnesia in Acute Herpetic and Nonherpetic Encephalitis
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The Inherited Ataxias and the New Genetics
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Risk Factors for Creutzfeldt-Jakob Disease:A Reanalysis of Case-Control Studies
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A New Variant of Creutzfeldt-Jakob Disease in the UK
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Intravenous IgG in Guillain-Barre Syndrome
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The"Gulf War Syndrome"-Is There Evidence of Dysfunction in the Nervous System
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Antiepileptic Drugs
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Evidence for Genetic Basis of Multiple Sclerosis
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Clinical and Subclinical Neurological Involvement in Children of Conjugal Multiple Sclerosis Patients
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Apolipoprotein E Genotyping in Alzheimer's Disease
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Presynaptic Dopaminergic Deficits in Lesch-Nyhan Disease
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Fatal Insomnia in a Case of Familial Creutzfeldt-Jakob Disease with the Codon 200Lys Mutation
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The Challenge of the Dementias
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Hearing Loss in a Memory Disorders Clinic:A Specially Vulnerable Population
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An 85-Year-Old Woman with a History of Falls
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Neuroradiologic Findings in Polyarteritis Nodosa
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Evidence-Based Medicine, Critical Pathways, Practice Guidelines, & Managed Care:Prevention & Care of Stroke
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Memory, Attention, and Executive Function in Chronic Fatigue Syndrome
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Routine Transesophageal Echocardiograhy for Cerebral Ischemia
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An Analysis of Lowest Effective Intensity of Prophylactic Anticoagulation for Pts with Nonrheumatic Atrial Fib
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Paraneoplastic Limbic Encephalitis in Hodgkin's Disease
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Clinical Spectrum of CADASIL:A Study of 7 Families
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New Phenotype of the Cerebral Autosomal Dominant Arteriopathy Mapped to Chromosome 19:Migraine as the Prominent Clinical Feature
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Leptomeningeal and Calvarial Sarcoidosis:CT and MR Appearances
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Familial Autoimmune Myasthenia Gravis:Report of Four Families
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