Spontaneous Dissections of Cervicocephalic Arteries in Childhood and Adolescence
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A Pediatric Case of Carotid Rete Mirabile
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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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Stroke and Cerebral Infarcts in Children Infected with Human Immunodeficiency Virus
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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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High Prevalence of Antiphospholipid Antibodies in Children with Idiopathic Cerebral Ischemia
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Trinucleotide Repeat Length and Rate of Progression of Huntington's Disease
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Mutation Analysis in Patients with Possible but Apparently Sporadic Huntington's Disease
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Trinucleotide Repeat Expansion in Neurological Disease
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Myotonic Dystrophy
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Cerebrotendinous Xanthomatosis:Molecular Diagnosis Enables Presymptomatic Detection of a Treatable Disease
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Attitudes Toward Direct Predictive Testing for the Huntington Disease Gene
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Neuroradiological Manifestations of Focal Polymorphic Delta Activity in Children
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Experience with Screening Newborns for Duchenne Muscular Dystrophy in Wales
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Ornithine Transcarbamylase Deficiency Presenting with Strokelike Episodes
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Molecular Genetic Advances in Fragile X Syndrome
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An Unusual Cause of Cerebral Venous Thrombosis in a Four-Year-Old Child
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Intracerebral Hemorrhage After Fibrinolytic Therapy for Acute Myocardial Infarction
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Clinical Consequences of Isolating the Gene for Huntington's Disease
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Rapid Diagnosis of Herpes Simplex Virus Encephalitis by Using the Polymerase Chain Reaction
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Analysis of Dystrophin Expression after Activation of Myogenesis in Amniocytes, Chorionic-Villus Cells, and Fibroblasts
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Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes (MELAS) :Clinical, Radiological, Pathol & Genetic Observ
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TORCH Infections in the Newborn
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Strokes in Children Due to Vertebral Artery Trauma
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Risk of Intracranial Hemorrhage & Adverse Outcomes-Cocaine Expose in 323 Very Low Birth Wt Infants
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Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test
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Tay-Sachs Disease-Carrier Screening, Prenatal Diagnosis, and the Molecular Era
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Molecular Genetics in Neurology
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The Polymerase Chain Reaction:Application to Nervous System Disease
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Surfactant Therapy and Intracranial Hemorrhage:Review of the Literature and Results of New Analyses
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The Psychological Consequences of Predictive Testing for Huntington's Disease
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Vascular Dysplasia in Down Syndrome:A Possible Relationship to Moyamoya Disease
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Girls with Fragile X Syndrome:Physical and Neurocognitive Status and Outcome
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Detection of Full Fragile X Mutation
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Value of Cranial Untrasound and MRI in Predicting Neurodevelopmental Outcome in Preterm Infants
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Effects of Intravent Hemorrhage & Socioecon Status on NEur Status of Low Birth Weight Inf at 5 yrs of age
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Trends in Perinatal MOrtality & Cerebral Palsy in Western Australia, 1967 to 1985
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Long-Term Outcome of Neonatal Meningitis
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Thalamic Lesions in Infancy
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Population Screening for Fragile X
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Superior Sagittal Sinus Thrombosis in a Child with Protein S Deficiency
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Cerebral Infarction Complicating Hemorrhagic Shock and Encephalopathy Syndrome
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Risk Factors for Early Intraventricular Hemorrhage in Low Birth Weight Infants
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Serial Changes of Cerebral Glucose Metab & Caudate Size in Persons at Risk for Huntington's Dis
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Infantile Panthalamic Infarct with a Striking Sonographic Finding:The"Bright Thalamus"
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Familial Neurofibromatosis Type 1:Clinical Experience with DNA Testing
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Screening for von Hippel-Lindau Disease by DNA Polymorphism Analysis
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Clinical Features of Vascular Thrombosis Following Varicella
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