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An unusual cause of stroke and hypoxia
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Unusual Variants of Alexander's Disease
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Parkinson's Disease
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Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients
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Hereditary Hemorrhagic Telangiectasia
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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
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Sturge-Weber Syndrome
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Alzheimers Disease
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Hypointensity of the Basal Ganglia in Adults with Glucose Transporter Protein Type 1 Deficiency Syndrome: A Novel Magnetic Resonance Imaging Finding
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Fibromuscular Dysplasia and Its Neurologic Manifestations
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Muscular Dystrophies
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Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
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Neuroradiologic Patterns and Novel Imaging Findings in Aicardi-Goutieres Syndrome
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Parkinson Disease Subtypes
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Sturge-Weber Syndrome and Port-Wine Stains Caused by Somatic Mutation in GNAQ
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GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
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A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
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Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
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Genomewide Association Studies of Stroke
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A 23-Year-Old Man With Seizures and Visual Deficit
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Tuberous Sclerosis
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The Tuberous Sclerosis Complex
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Von Recklinghausen's Neurofibromatosis: Neurofibromatosis Type 1
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Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
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New Players in the Genetics of Stroke
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Impact of the Human Genome Projects and Identification of a Stroke Gene
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New Developments in the Neurobiology of the Tuberous Sclerosis Complex
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Creutzfeldt-Jakob Disease in a Young Woman
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Clinical Spectrum of CADASIL:A Study of 7 Families
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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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DNA Diagnosis of Neurofibromatosis 2:Altered Coding Sequence of the Merlin Tumor Suppressor in an Extended Pedigree
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Wilson Disease
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Mutation in Cystatin C Gene Causes Hereditary Brain Hemorrhage
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Anderson-Fabray Disease, A Commonly Missed Diagnosis
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Cavernous Maliformations of the Central Nervous System
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Neuroimaging Features of Biotinidase Deficiency
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