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A 50-YEar-Old Man with Intracerebral Hemorrhage and Tortuous Retinal Arterioles
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Neurological Management of Von Hippel-Lindau Disease
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Degenerative Diseases of the Nervous System, Friedreich Ataxia
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GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
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Genetic Aspects of Alzheimer Disease
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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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The Tuberous Sclerosis Complex
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Sensorineural Hearing Loss in Children
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Association of Multidrug Resistance in Epilepsy with a Polymorphism in the Drug-Transporter Gene ABCB1
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Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
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The Clinical Spectrum of Familial Hemiplegic Migraine Associated with Mutations in a Neuronal Calcium Channel
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Ion Channel Diseases:Episodic Disorders of the Nervous System
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Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
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The Muscular Dystrophies
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
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Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
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Clinical Genetics in Neurological Disease
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Leber's Hereditary Optic Neuropathy as a Cause of Severe Visual Loss in Childhood
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