Migraine:Theories of Pathogenesis
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Neonatal Seizures
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Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
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Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
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Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
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Duchenne Muscular Dystrophy
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A 22-Year-Old Man with Progressive Bilateral Visual Loss
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A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
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Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
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A 58-year-old Man with Hand Tremor and Episodes of Neck Pain
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Ehlers-Danlos Syndromes
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Muscular Dystrophies
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Neuroimaging Changes in Menkes Disease, Part 1
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A 44-Year-Old Man with Eye, Kidney, and Brain Dysfunction
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Neurological Management of Von Hippel-Lindau Disease
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Mystery Case: A 21-Year-Old Man with Visual Loss Following Marijuana Use
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Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Red Papules on the Tongue of a Patient with Hemiparesis
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Degenerative Diseases of the Nervous System, Machado-Joseph-Azorean Disease
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Efficacy and Safety of Everolimus for Subependymal Giant Cell Astrocytomas Associated with Tuberous Sclerosis Complex (EXIST-1): A Multicenter, Randomized, Placebo-Controlled Phase 3 Trial
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Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Neurofibromatosis Type 2
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The Hot Cross Bun Sign in the Patients with Spinocerebellar Ataxia
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Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
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MR Imaging of Familial Creutzfeldt-Jakob Disease: A Blinded and Controlled Study
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Two Sets of Identical Twins with Cervical Artery Dissection Concordant for Temporal Artery Pathology
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Pulmonary Arteriovenous Malformations in Hereditary Hemorrhagic Telangiectasia: A Series of 126 Patients
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Neuroimaging Findings in Human Prion Disease
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The Tuberous Sclerosis Complex
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Brain Magnetic Resonance Imaging in Patients with Cowden Syndrome
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Cerebroretinal Vasculopathy Mimicking a Brain Tumor:A Case of a Rare Hereditary Syndrome
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The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
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Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
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Clinical and Genetic Studies of Fatal Familial Insomnia
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Hereditary Hemorrhagic Telangiectasia
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Inclusion Body Myositis and Myopathies
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Congential Deficienty of Factor VII in Subarachnoid Hemorrhage
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Familial Autoimmune Myasthenia Gravis
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Neurovascular Manifestations of Heritable Connective Tissue Disorders:A Review
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Progressive Multifocal Leukoencephalopathy Complicating Wiskott-Aldrich Syndrome
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Clin & Path Features of an Autosomal Dominant, Adult-Onset Leukodystrophy Simul Chronic Progressive MS
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