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Neurological Complications of Infantile Osteopetrosis
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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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Hypotonia and Delayed Teeth Eruption in a 2-Year-Old Girl
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Congenital Cytomegalovirus Infection
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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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Bannayan-Riley-Ruvalcaba Syndrome: MRI Neuroimaging Features in a Series of 7 Patients
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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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The Epilepsy of Trisomy 9p
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The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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Angelman Syndrome: Clinical Profile
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Congenital Inflammatory Myopathy
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Periventricular-Intraventricular Hemorrhage Sonographic Localization in Low Birth Weight Infants
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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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Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
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