Clinicopath conf., Human Prion Disease, Sporadic CJD
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Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease
JAMA Neurol 73:668-674, Martikainen, M.H.,et al, 2016
Clinical Spectrum of Ataxia-Telangiectasia in Adulthood
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991
A 37-Year-Old Man with Involuntary Movements, Gait Disturbance, and Hyperasthesia
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Muscle Stiffness, Gait Instability, and Liver Cirrhosis in Wilsons Disease
Lancet 396:990, Kronlage, C.,et al, 2020
Neurodegeneration with Brain Iron Accumulation
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Paraneoplastic and Autoimmune Encephalitis
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Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
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Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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Wilson Disease
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Inherited Metabolic Diseases of the Nervous System, Hepatolenticular Degeneration (Wilson Disease)
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Criteria for the Diagnosis of Corticobasal Degeneration
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Incidence and Pathology of Synucleinopathies and Tauopathies Related to Parkinsonism
JAMA Neurol 70:859-866, Savica, R.,et al, 2013
Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
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Tau Forms in CSF as a Reliable Biomarker for Progressive Supranuclear Palsy
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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Out of Africa, Trypanosomiasis
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Niemann-Pick Disease Type C: Two Cases and an Update
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Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Familial Idiopathic Striopallidodentate Calcifications
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Late Onset of Distinct Neurologic Syndromes in Galactosemic Siblings
Neurol 39:741-742, Friedman,J.H.,et al, 1989
Creutzfeldt-Jakob Disease without Periodic Sharp Wave Complexes:A Clinical, EEG, and Path Study
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Clinicopathological Conference
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A Family with Hereditary Ataxia:HLA Typing
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Normal Pressure Hydrocephalus, Recog & Relation to Neuro Abnormalities in Cockayne's Sydrome
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Elevated Manganese Levels Associated with Dementia & Extrapyramidal Signs
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Huntington's Chorea
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