Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
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Spinal Muscular Atrophy
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Neurodevelopment and Cognition in Children After Enterovirus 71 Infection
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Neurologic and Developmental Disability After Extremely Preterm Birth
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Neurodevelopmental Outcome of Infants with Hypoplastic Left Heart Syndrome
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Significance of Seizures Associated with Extracorporeal Membrane Oxygenation
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Neurological Deterioration in Young Adults with Phenylketonuria
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Brain Damage by Neonatal Hypoglycaemia
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Infantile Epileptic Spasms Syndrome (West Syndrome)
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A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
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A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
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The Phenotypic Continuum of ATP1A3-Related Disorders
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Duchenne Muscular Dystrophy
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Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
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Neurodegeneration with Brain Iron Accumulation
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A 13-year-old boy with Chronic Ataxia and Developmental Delay
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A Woman with Intellectual Disability, Amenorrhoea, Seizures, and Balance Problems
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Molybdenum Cofactor Deficiency
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Sturge-Weber Syndrome
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Early Child Development and Exposure to Antiepileptic Drugs Prenatally and Through Breastfeeding
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Sturge-Weber Syndrome
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Clinicopath Conf, Infantile Krabbe Disease
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MRI in Methylmalonic Acidemia
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Case 35-2006: A Newborn Boy with Hypotonia
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Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
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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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Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
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The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
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Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes (MELAS) :Clinical, Radiological, Pathol & Genetic Observ
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Gray Matter Heterotopias:MR Characteristics & Correlation with Develop & Neurologic Manifest
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Congenital Muscular Dystrophy
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Recognising & Preventing Duchenne Muscular Dystrophy
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Diagnostic Delay in Duchenne's Muscular Dystrophy
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Neurological Complications of Infantile Osteopetrosis
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