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Neurological Management of Von Hippel-Lindau Disease
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Cavernous Maliformations of the Central Nervous System
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Review of the Neurological Implications of von Hippel-Lindau Disease
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Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
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A 50-YEar-Old Man with Intracerebral Hemorrhage and Tortuous Retinal Arterioles
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A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
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Brain Tumors in Children
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Updates on Sturge-Weber Syndrome
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A 14-Year-Old Girl with Headache, Seizures, and Confusion
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A Teenager with Persistent Headache
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Clinicopathologic Conference, Homocystinuria due to genetic mutations of the gene encoding cystathionine B-synthase (CBS)
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Characyeristic features and progression of abnormalities on MRI for CARASIL
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A 27-Year Old Man with Rapidly Progressive Coma
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Primary CNS T-Cell Lymphomas: A Clinical, Morphologic, Immonophenotypic and Molecular Analysis
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Cerebral Abnormalities in Adults with Ataxia-Telangiectasia
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Bannayan-Riley-Ruvalcaba Syndrome: MRI Neuroimaging Features in a Series of 7 Patients
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Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Clinicopathologic Conference, Severe Methylenetetrahydrofolate Reductase Deficiency
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Sturge-Weber Syndrome
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Intracranial Neoplasms and Paraneoplastic Disorders, Meningioma
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Sturge-Weber Syndrome
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Recent Insights into Cerebral Cavernous Malformations: The Molecular Genetics of CCM
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Neurologic Manifestations of von Hippel-Lindau Disease
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Outcome in Adult Low-Grade Glioma: The Impact of Prognostic Factors and Treatment
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Role of COL4A1 in Small-Vessel Disease and Hemorrhagic Stroke
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Hyperhomocysteinemia, Low Folate and Vitamin B12 Concentrations, and Methylene Tetrahydrofolate Reductase Mutation in Cerebral Venous Thrombosis
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Hyperhomocysteinemia in Cerebral Vein Thrombosis
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Primary Anaplastic Large Cell Lymphoma of the Central Nervous System
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Expression of p53 and Prognosis in Children With Malignant Gliomas
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Factor V Leiden Mutation is a Risk Factor for Cerebral Venous Thrombosis,A Case-Control Study of 55 Patients
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Cerebral Venous Sinus Thrombosis Associated with Factor V Gene Mutation
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Molecular Genetics in Neurology
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