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Genetic Testing of Children at Risk for Huntington's Disease
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Few Psychological Consequences of Presymptomatic Testing for Huntington Disease
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The Clinical Introduction of Genetic Testing for Alzheimer Disease, An Ethical Perspective
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Preclinical Evidence of Alzheimer's Disease in Persons Homozygous for the e4Allele for Apolipoprotein E
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Motor Changes in Presymptomatic Huntington Disease Gene Carriers
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High Apolipoprotein E e4 Allele Frequency in Age-Related Memory Decline
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Statement of Use of Apolipoprotein E Testing for Alzheimer Disease
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A Low, "Normal"Score on the Mini-Mental State Exam Predicts Development of Dementia after Three Years
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Neuropsychological Detection and Characterization of Preclinical Alzheimer's Disease
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Reduced Basal Ganglia Volume Associated with the Gene for Huntington's Disease in Asymptomatic at-Risk Persons
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The Neurogenetic Genie:Testing for Huntington's Disease Mutation
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A Worldwide Study of the Huntington's Disease Mutation, The Sensitivity & Specificity of Measuring CAG Repeats
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Attitudes Toward Direct Predictive Testing for the Huntington Disease Gene
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Clinical Consequences of Isolating the Gene for Huntington's Disease
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Serial Changes of Cerebral Glucose Metab & Caudate Size in Persons at Risk for Huntington's Dis
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Presymptomatic Testing for Huntington's Disease in the United Kingdom
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The Psychological Consequences of Predictive Testing for Huntington's Disease
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Genetic Testing for Huntington's Disease
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Abnormalities of Striatal Projection Neurons and n-Methyl-d-Aspartate Receptors in Presymptomatic Huntington's Disease
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Predictive Testing for Huntington's Disease with Linked DNA Markers
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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, Progress and Problems
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Adoption and Genetic Prediction for Huntington's Disease
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Predictive Testing for Huntington's Disease with Use of a Linked DNA Marker
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Presymptomatic Neuropsychological Impairment in Huntington's Disease
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Normal Caudate Glucose Metabolism in Persons at Risk for Huntington's Disease
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Reduced Cerebral Glucose Metabolism in Asymptomatic Subjects at Risk for Huntington's Disease
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The Combined Use of Positron Emission Tomography & DNA Polymorphisms for Preclinical Detection of Huntington's Disease
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Positron Emission Tomography in the Early Diagnosis of Huntington's Disease
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Huntington's Disease, Pathogenesis & Management
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A DNA Polymorphism for Huntington's Disease Marks the Future
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Presymptomatic Testing for Huntington's Disease
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Genetic Prediction & Family Structure in Huntington's Chorea
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Genetic Testing in Huntington's Disease
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A Genetic Marker for Huntington's Chorea
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Attitudes Of Those At Risk For Huntington's Disease Toward Presymptomatic Provocative Testing
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Huntington's Disease, CSF GABA Level in at-risk Individuals
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Photophobia as the Presenting Symptom of Internal Carotid Artery Dissection
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Stroke Risk after Emergency Department Treat-and-Release Visit for a Fall
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Parkinsons Disease
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A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
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Wearable Digital Health Technology for Epilepsy
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Rabbit Syndrome
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Anti-NMDA Receptor Encephalitis Presenting with Cerebellitis in a Pediatric Patient
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Association of Coffee Consumption and Prediagnostic Caffeine Metabolites with Incident Parkinson Disease in a Population-Based Cohort
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Treatment Modalities and Outcomes in Brainstem Cavernous Malformations: A Large Multicenter Observational Cohort Study
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Vascular Malformations of the Central Nervous System
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Epilepsy in Patients with Primary CNS Lymphoma, Prevalence, Risk Factors, and Prognostic Significance
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