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Developmental Neurotoxivity of Industrial Chemicals
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The Relation of Transient Hypothyroxinemia in Preterm Infants to Neurologic Development at Two Years of Age
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Methylmercury Poisoning:Long-Term Clinical, Radiological, Toxicological, and Pathological Studies of an Affected Family
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Neurological Involvement in the Epidermal Naevus Syndrome
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School Failure & Deafness After"Silent"Congenital Cytomegalovirus Infection
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The Thyroid Gland:Its Relationship to Neurology
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Infantile Spasms Favorable Response to Steroid Therapy
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Screening for Inborn Errors of Metabolism Associated with Mental Deficiency or Neurologic Disorders or Both
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The Natural Hx of Infantile Spasms
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Newborn Screening for Fragile X Syndrome
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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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Range of Genetic Mutations Associated with Severe Non-Syndromic Sporadic Intellectual Disability: An Exome Sequencing Study
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Diagnostic Exome, Sequencing in Persons with Severe Intellectual Disability
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Epilepsy in Children with Infantile Thiamine Deficiency
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Extension of the Clinical Spectrum of Danon Disease
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Overview of Phenylketonuria
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Mirror Writing: Neurological Reflections on an Unusual Phenomenon
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Angelman Syndrome Revisited
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Phenylketonuria
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Oligophrenin 1 Mutations Frequently Cause X-Linked Mental Retardation with Cerebellar Hypoplasia
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Diffusion-Weighted Imaging and Proton MR Spectroscopy of White Matter Abnormalities in a Case of Phenylketonuria
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Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
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