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Mitochondrial Respiratory-Chain Diseases
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Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
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Progressive Pontobulbar Palsy With Deafness
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Criteria for the Diagnosis of Corticobasal Degeneration
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Differential Diagnosis of Bilateral Abnormalities of the Basal Ganglia and Thalamus
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Progressive Supranuclear Palsy: A Current Review
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Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
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Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
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Familial Multisystem Atrophy with Possible Thalamic Dementia
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Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
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Familial Subacute Necrotizing Encephalomyelopathy of the Adult Form (Adult Leigh Syndrome)
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Azorean Disease of the Nervous System
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Progressive Supranuclear Palsy Clinico-Pathological Study of Four Cases
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Corticodentatonigral Degeneration with Neuronal Achromasia
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Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction
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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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Clinicopathologic Conference, Primary Progressive Aphasia, Semantic Variant, due to TAR DNA Binding Protein 43 associated Frontotemporal Lobar Degen
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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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Clinicopathologic Conference, Frontotemporal Lobar Degeneration with Tau-positive Inclusions (Picks Disease Subtype) Due to a Gly389Arg MAPT Mutation, Resulting in the Behavioral Variant of Frontotemporal Dementia with Parkinsonism
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T2* and FSE MRI Distinguishes Four Subtypes of Neurodegeneration With Brain Iron Accumulation
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Neuroimaging Findings in Human Prion Disease
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Amyotrophic Lateral Sclerosis
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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MR Features of Diseases Involving Bilateral Middle Cerebellar Peduncles
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Cholinergic Vesicular Transporters in Progressive Supranuclesar Palsy
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Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
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Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
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Apolipoprotein E Genotype in Diverse Neurodegenerative Disorders
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Magnetic Resonance Imaging of Brain Iron in Health and Disease
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Excitatory Amino Acids as a Final Common Pathway for Neurologic Disorders
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Chronic Neurodegenerative Disease Associated with HTLV-II Infection
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Infantile CNS Spongy Degeneration-14 Cases:Clinical Update
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Sleep Abnormalities in Progressive Supranuclear Palsy
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Neurological Clues from Environmental Neurotoxins
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