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Sturge-Weber Syndrome
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Inherited Metabolic Diseases of the Nervous System, The Phenylketonuria
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The Ever-Expanding Spectrum of Congenital Muscular Dystrophies
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Transition to Adult Care for Children with Chronic Neurological Disorders
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Overview of Phenylketonuria
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Congenital Lymphocytic Choriomeningitis Virus Infection: Spectrum of Disease
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Phenylketonuria
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The Tuberous Sclerosis Complex
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Developmental Neurotoxivity of Industrial Chemicals
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Prader-Willi and Angelman Syndromes
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The Relation of Transient Hypothyroxinemia in Preterm Infants to Neurologic Development at Two Years of Age
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Prenatal Magnesium Sulfate Expos/Risk for CP or MR Among Very Low-Birth-Weight Child Aged 3-5 Yrs
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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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Prenatal Alcohol Exposure and Long-Term Developmental Consequences
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Neuroleptics, Learning Disability, and the Community:Some History and Mystery
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Alternating Hemiplegia of Childhood
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Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test
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Mental Development of 2-Year-Old Children Exposed to Alcohol in Utero
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Girls with Fragile X Syndrome:Physical and Neurocognitive Status and Outcome
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Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental Retardation
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Prenatal Diagnosis of Fragile X Syndrome by Direct Detection of the Unstable DNA Sequence
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Perinatal Loss and Neurological Abnormalities Among Children of the Atomic Bomb
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Valproic Acid for the Treatment of Children with Mental Retardation and Mood Symptomatology
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Efficacy of Methylphenidate Among Mentally Retarded Children with Attention Deficit Hyperactivity Disorder
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