GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
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Guillain-Barre Syndrome with Hydrocephalus in Early Infancy
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Neurological Complications of Infantile Osteopetrosis
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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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Clinicopathologic Conference, Aqueductal Stenosis with Hydrocephalus
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Cognitive Delay in a 7-year-old Girl
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Neurodevelopmental Dysfunction Among Nonreferred Children with Idiopathic Megalencephaly
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Outlook for the Child with a Cephalocele
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Infantile CNS Spongy Degeneration-14 Cases:Clinical Update
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Hunter Disease (Mucopolysaccharidosis Type II) in a Karyotypically Normal Girl
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Cavum Vergae, Association with Neurologic Abnormality & Diagnosis by Magnetic Resonance Imaging
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Alexander's Disease, A Disease of Astrocytes
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Clin. Path. Conference
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Progressive Focal Deficit with Porencephaly
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