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Neurofibromatosis 2 (Bilateral Acoustic Neuro-fibromatosis)
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Detection Of Adrenoleucodystrophy Carriers By Means Of Evoked Potentials
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Non-Alzheimers Dementia 1 Frontotemporal Dementia
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A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
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Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
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Imaging Patterns Characterizing Mitochondrial Leukodystrophies
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Clinicopathologic Conference, Vascular Malformations in Liver, Stomach, Esophagus, and Lungs that are Consistent with Hereditary Hemorrhagic Telangiectasia, Complicated
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Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
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A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
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Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
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Neurological Management of Von Hippel-Lindau Disease
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DARS-Associated Leukoencephalopathy can Mimic a Steroid-Responsive Neuroinflammatory Disorder
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Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Restricted Diffusion in Vanishing White Matter
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Prevalence of Fabry Disease in Patients with Cryptogenic Stroke: A Prospective Study
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Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene
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Brain Magnetic Resonance Imaging in Patients with Cowden Syndrome
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Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
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Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
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Autosomal Dominant Acute Necrotizing Encephalopathy
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Mutations in Each of the Five Subunits of Translation Initiation Factor eIF2B Can Cause Leukoencephalopathy with Vanishing White Matter
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Adult-Onset Leukoencephalopathy with Vanishing White Matter Presenting with Dementia
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Distribution of Cranial MRI Abnormalities in Patients with Symptomatic and Subclinical CADASIL
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Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
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Hereditary Cerebral Cavernous Angiomas:Clinical and Genetic Features in 57 French Families
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Linkiage of Locus for Cerebral Cavernous Hemagiomas to Chromosome 7q in 4 Families of Mexican-American Descent
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Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
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Screening Family Members of Patients with Hereditary Hemorrhagic Telangiectasia
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Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
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Turcot's Syndrome:Evidence for Linkage to the Adenomatous Polyposis Coli (APC) Locus
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Progressive Vison Loss, A Rare Manifestation of Familial Cavernous Angiomas
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Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
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Cortically Evoked Motor Responses in Patients with Xp22. 3-Linked Kallmann's Syndrome and in Female Gene Carriers
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Central Nervous System Lesions in von Hippel-Lindau Syndrome
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Central Nervous System Involvement in Von Hippel-Lindau Disease
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