More Than a Little Unsteady
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A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
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Degenerative Diseases of the Nervous System, Familial Dementia with Spastic Paraparesis
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Frontotemporal Dementia is on the MAP
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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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Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
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Chromosome 14-Encoded Alzheimer's Disease:Genetic and Clinicopathological Description
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Real and Imagined Clinicopathological Limits of"Prior Dementia"
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Infectious Prions or Cytotoxic Metabolites?
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The Spongiform Encephalopathies, Editorial
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Prion Dementia Without Characteristic Pathology
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Familial Alzheimer's Disease with Myoclonus and'Spongy Change'
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