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CNS Involvement at the Onset of Primary Hemophagocytic Lymphohistiocytosis
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Neurologic Manifestations of von Hippel-Lindau Disease
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Primary Brain Tumours in Adults
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Conjugal Temporal Arteritis
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Mendelian Etiologies of Stroke
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A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
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Focusing on the Eye Signs of Alport Syndrome in a 40-Year-Old Man Who Previously Had a Kidney Transplant and Hearing Loss
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Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
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A 14-Year-Old Girl with Headache, Seizures, and Confusion
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Neuromyelitis Optica Spectrum Disorders
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Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
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Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Intracranial Neoplasms and Paraneoplastic Disorders, Meningioma
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Inherited Metabolic Diseases of the Nervous System, Adrenoleukodystrophy
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Brain Arteriovenous Malformation Multiplicity Predicts the Diagnosis of Hereditary Hemorrhagic Telangiectasia Quantitive Assessment
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Comparison of Clinical, Familial, and MRI Features of CADASIL and NOTCH3-Negative Patients
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Genetic Aspects of Alzheimer Disease
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Leukodystrophies: Classification, Diagnosis, and Treatment
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Familiality in Brain Tumors
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Fatal Avian Influenza A (H5N1) in a Child Presenting with Diarrhea Followed by Coma
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Recurrent Acroparaesthesia During Febrile Infections
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Hereditary Infantile Hemiparesis, Retinal Arteriolar Tortuosity, and Leukoencephalopathy
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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
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Cerebroretinal Vasculopathy Mimicking a Brain Tumor:A Case of a Rare Hereditary Syndrome
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Distal Hereditary Upper Limb Muscular Atrophy
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Hematopoietic Stem-Cell Transplantation in Globoid-Cell Leukodystrophy
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Prognosis in Familial ALS:Progr & Surv in Pts with glu100gly & ala4val Mutations in Cu, Zn Superoxide Dismutase
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Adult-Onset Krabbe's Disease in Siblings with Novel Mutations in the Galactocerebrosidase Gene
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CT and MR Findings of Neuroacanthocytosis
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Adult-Onset Neimann-Pick Type C Disease, Clinical, Biochemical and Genetic Study
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Niemann-Pick Disease Type C from Bench to Bedside
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X-Linked Malformation of Neuronal Migration
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Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
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