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Recurrent Cerebral Ischemia During Pregnancies
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Fibromuscular Dysplasia and Its Neurologic Manifestations
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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Amyotrophic Lateral Sclerosis
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Degenerative Diseases of the Nervous System, Parkinson Disease
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GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
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Aicardi-Gouti�res Syndrome
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Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
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A 23-Year-Old Man With Seizures and Visual Deficit
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Genetics of Parkinsons Disease and Parkinsonism
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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Association of Multidrug Resistance in Epilepsy with a Polymorphism in the Drug-Transporter Gene ABCB1
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Association Between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
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Molecular Genetic Heterogeneity of Myophosphorylase Deficiency (McArdle's Disease)
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Charcot-Marie-Tooth Disease Type 1A:Association with a Spontaneous Point Mutation in the PMP22 Gene
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Miller-Dieker Syndrome:Detection of a Cryptic Chromosome Translocation Using in Situ Hybridization in a Family
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