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GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
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Prader-Willi and Angelman Syndromes
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Congenital AIDS:Review of Neurological Problems
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Alexander's Disease, A Disease of Astrocytes
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Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
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Neuroimaging Changes in Menkes Disease, Part 1
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Inherited Metabolic Diseases of the Nervous System, Galactosemia
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Cystic Fibrosis Presenting With Intracerebral Haemorrhage
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Leukotriene C4-synthesis Deficiency:A New Inborn Error of Metabolism Linked to a Fatal Developmental Syndrome
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Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes (MELAS) :Clinical, Radiological, Pathol & Genetic Observ
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MR of Progressive Neurodegenerative Change in Treated Menkes'Kinky Hair Disease
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Carbonic Anhydrase II Deficiency in 12 Families with Osteopetrosis with Renal Tubular Acidosis & Cerebral Calcification
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