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Sturge-Weber Syndrome
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The Ever-Expanding Spectrum of Congenital Muscular Dystrophies
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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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The Tuberous Sclerosis Complex
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Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
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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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Methylmercury Poisoning:Long-Term Clinical, Radiological, Toxicological, and Pathological Studies of an Affected Family
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Neuroleptics, Learning Disability, and the Community:Some History and Mystery
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Girls with Fragile X Syndrome:Physical and Neurocognitive Status and Outcome
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Fucosidosis Revisited:A Review of 77 Patients
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A Follow-up Study of Intractable Seizures in Childhood
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Sulfite Oxidase Deficiency:Clinical, Neuroradiologic, and Biochemical Features in Two New Patients
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Prospective Study of Outcome of Infants with Infantile Spasms Treated During Studies of ACTH & Prednisone
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Neurological Manifestations in Xeroderma Pigmentosum
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Alexander's Disease, A Disease of Astrocytes
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Familial Chorea & Myoclonus Epilepsy
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Psychological Management of the Retarded Child & Its Family
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