A Case of Early-Onset Rapidly Progressive Dementia
JAMA Neurol 71:1445-1449, Cachia, D.,et al, 2014
Sporadic Creutzfeldt-Jakob Disease in a Very Young Person
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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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Non-Alzheimers Dementia 1 Frontotemporal Dementia
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Progressive Neuropsychiatric Symptoms and Motor Impairment
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Clinical Characteristics of a Chromosome 17-Linked Rapidly Progressive Familial Frontotemporal Dementia
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Atypical Alzheimer's Disease with Spastic Paresis & Ataxia
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Elevated Manganese Levels Associated with Dementia & Extrapyramidal Signs
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