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A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
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A New Variant of Creutzfeldt-Jakob Disease in the UK
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Neurodegenerative Disease Mortality Among Former Professional Soccer Players
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Pantothenate Kinase - Associated Neurodegeneration (PKAN)
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Amyotrophic Lateral Sclerosis
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Dentate Update: Imaging Features of Entities that Affect the Dentate Nucleus
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Intrathecal 2-hydroxypropyl-�-cyclodextrin Decreases Neurological Disease Progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial
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A Young Man with Progressive Language Difficulty and Early-Onset Dementia
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Criteria for the Diagnosis of Corticobasal Degeneration
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Clinical Reasoning: A Woman with Rapidly Progressive Apraxia
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Ataxia, Dementia, and Hypogonadotropism Caused by Disordered Ubiquitination
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The Spectrum of Mutations in Progranulin: A Collaborative Study Screening 545 Cases of Neurodegeneration
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Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
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Progressive Supranuclear Palsy: A Current Review
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Neuroimaging Findings in Human Prion Disease
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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Mitochondrial Respiratory-Chain Diseases
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The Topography of Metabolic Deficits in Posterior Cortical Atrophy (the Visual Variant of Alzheimers Disease) with FDG-PET
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Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
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CSF Detection of the 14-3-3 Protein in Unselected Patients with Dementia
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Positron Emission Tomography in Evaluation of Dementia
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Molecular Basis of the Neurodegenerative Disorders
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Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
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Frontotemporal Degeneration, Pick Disease, and Corticobasal Degeneration
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Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease
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Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
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Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
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Trinucleotide Repeat Expansion in Neurological Disease
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The Apolipoprotein E Alleles as Major Susceptibility Factors for Creutzfeldt-Jakob Disease
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Protein Processing in Lysosomes:The New Therapeutic Target in Neurodegenerative Disease
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Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
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