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Cavernous Maliformations of the Central Nervous System
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
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Amyotrophic Lateral Sclerosis
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Linkage of a Gene Causing Familial ALS to Chromosome 21 & Evidence of Genetic-Locus Heterogeneity
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Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
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A 50-YEar-Old Man with Intracerebral Hemorrhage and Tortuous Retinal Arterioles
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Neuroimaging Features of Biotinidase Deficiency
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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
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Alzheimers Disease
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Clinical and Genetic Features in Patients with Reflex Bathing Epilepsy
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Genetics of Cluster Headache Takes a Leap
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Fibromuscular Dysplasia and Its Neurologic Manifestations
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Ehlers-Danlos Syndromes
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Amyotrophic Lateral Sclerosis
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Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
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MRI Findings of Biotin-Responsive Basal Ganglia Disease Before and After Treatment
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Parkinson Disease Subtypes
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Degenerative Diseases of the Nervous System, Parkinson Disease
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Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety
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Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability
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Whole-Genome Sequencing in a Patient with Charcot-Marie-Tooth Neuropathy
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Genetic Aspects of Alzheimer Disease
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