A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
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Cognitive Delay in a 7-year-old Girl
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GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
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Subarachnoid Fluid Collections:A Cause of Macrocrania in Preterm Infants
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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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Outlook for the Child with a Cephalocele
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Hunter Disease (Mucopolysaccharidosis Type II) in a Karyotypically Normal Girl
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Neonatal Brain Tumors:CT & MR Findings
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The Dandy-Walker Syndrome
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Cavum Vergae, Association with Neurologic Abnormality & Diagnosis by Magnetic Resonance Imaging
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GM1 Gangliosidosis:Clinical and Laboratory Findings in Eight Families
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Alexander's Disease, A Disease of Astrocytes
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Neurological Complications of Infantile Osteopetrosis
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