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Congenital Cytomegalovirus Infection
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A Child with Arthrogryposis
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Pyruvate Dehydrogenase Deficiency (PDCD)
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A Child with Delayed Motor Milestones and Ptosis
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Molybdenum Cofactor Deficiency
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Sturge-Weber Syndrome
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Aromatic L-Amino Acid Decarboxylase Deficiency
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New Developments in the Neurobiology of the Tuberous Sclerosis Complex
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Management Issues for Women with Epilepsy,A Review of the Literature
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An Early Marker for Neurological Deficits after Perinatal Brain Lesions
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Valproic Acid Hepatic Fatalities. III. U. S. Experience Since 1986
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Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
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Neurologic Status of HIV-1 Infected Infants and Their Controls:A Prospective Study from Birth to 2 Yrs
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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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A Synd of Autosomal Dominant Alternating Hemiplegia:Mimicking Intractable Epilepsy; Chromosomal Studies; Physiol Investig
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Angelman Syndrome: Clinical Profile
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A Clinical Study of Noonan Syndrome
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Defective Glucose Transport Across the Blood-Brain Barrier as Cause of Hypoglycorrhachia, Seizures, and Devel Delay
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