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Criteria for the Diagnosis of Corticobasal Degeneration
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Cognitive and Clinical Characteristics of Patients with Limbic-Predominant Age-Related TDP-43 Encephalopathy
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Multiple-System Atrophy
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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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Differential Diagnosis of Bilateral Abnormalities of the Basal Ganglia and Thalamus
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A 75-Year-Old Woman with Progressive Right-Hand Tremor and Inability to Use Her Right Side
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Progressive Supranuclear Palsy: A Current Review
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Rapidly Progressive Dementia
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Neuroimaging Findings in Human Prion Disease
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Amyotrophic Lateral Sclerosis
Lancet 369:2031-2041, Mitchell,J.D. & Borasio,G.D., 2007
MR Features of Diseases Involving Bilateral Middle Cerebellar Peduncles
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Neurodegenerative Diseases and Prions
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CSF Detection of the 14-3-3 Protein in Unselected Patients with Dementia
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Pathologic Heterogeneity in Clinically Diagnosed Corticobasal Degeneration
Neurol 53:795-800, Boeve,B.F.,et al, 1999
Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998
Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease
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A New Variant of Creutzfeldt-Jakob Disease in the UK
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Molecular Genetics in Neurology
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The Polymerase Chain Reaction:Application to Nervous System Disease
Ann Neurol 34:513-523, Darnell,R.B., 1993
Gene Therapy for Neurologic Disease
Arch Neurol 50:1252-1268, Suhr,S.T.&Gage,F.H., 1993
Mutation of the Prion Protein in Libyan Jews with Creutzfeldt-Jakob Disease
NEJM 324:1091-1097, Hsiao,K.,et al, 1991
Rapid Detection of Creutzfeldt-Jakob Disease and Scrapie Prion Porteins
Neurol 40:110-117, Serban,D.,et al, 1990
Inherited Human Prion Diseases
Neurol 40:1820-1827, Hsiao,K.&Prusiner,S.B., 1990
Prions & Neurodegenerative Diseases
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