Fibromuscular Dysplasia and Its Neurologic Manifestations
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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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A 23-Year-Old Man With Seizures and Visual Deficit
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Variable Presentation of Brugada Syndrome: Lessons from Three Generations with Syncope
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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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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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MRI Findings of Biotin-Responsive Basal Ganglia Disease Before and After Treatment
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Neurological Management of Von Hippel-Lindau Disease
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Degenerative Diseases of the Nervous System, Alzheimer Disease
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Parkin Disease
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Genes Associated With Adult Cerebral Venous Thrombosis
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An unusual cause of stroke and hypoxia
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A Multidisciplinary Study of Patients with Early-Onset PD with and Without Parkin Mutations
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Aicardi-Gouti�res Syndrome
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Autosomal Dominant Moyamoya Disease Maps to Chromosome 17q25.3
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Tuberous Sclerosis
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Parkinsons Disease and Genetics
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The Tuberous Sclerosis Complex
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
NEJM 348:33-40, Hayflick,S.J.,et al, 2003
Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
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Complete Genomic Screen in Parkinson Disease
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Association Between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene
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New Developments in the Neurobiology of the Tuberous Sclerosis Complex
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Clinical Spectrum of CADASIL:A Study of 7 Families
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Hereditary Hemorrhagic Telangiectasia
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Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
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Neurofibromatosis 2:Clinical & DNA Linkage Studies of a Large Kindred
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