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Late-Onset Hallervorden-Spatz Disease Presenting as Familial Parkinsonism
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Pantothenate Kinase - Associated Neurodegeneration (PKAN)
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Genetic Studies on Chromosome 12 in Late-Onset Alzheimer Disease
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Evidence for an Alzheimer Disease Susceptability Locus on Chromosome 12 and for Further Locus Heterogeneity
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Clinicopath Conf
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Magnetic Resonance Imaging in Pathologically Proven Hallervorden-Spatz Disease
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Mineralization of the Basal Ganglia Detected by CT in Hallervorden-Spatz Syndrome
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Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features
Ann Neurol 3:419, Dorfman,L.J.,et al, 1978
A 30-Year-Old Woman Presenting with Rapidly Progressive Dementia and Extreme Hypoglycorrhachia
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A 51-Year-Old Woman with Abnormal Corups Callosum Signal
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Lecanemab in Early Alzheimers Disease
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Cognitive and Clinical Characteristics of Patients with Limbic-Predominant Age-Related TDP-43 Encephalopathy
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Clinicopathologic Conference, Cerebral Amyloid Angiopatny-Related Inflammation
NEJM 385:358-368, Case 22-2021, 2021
Vitamin B12 Deficiency in a 29-Year-Old Woman
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Sporadic Creutzfeldt-Jakob Disease in a Very Young Person
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Epilepsy in Older People
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A 42-year-old Woman with Progressive Cognitive Difficulties and Gait Imbalance
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Limbic-Predominant Age-Related TDP-43 Encephalopathy (LATE): Consensus Working Group Report
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Debate Sparks Over LATE, a Recently Recognized Dementia
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Progressive Proximal Weakness in a 56-year-old Man with Bone Pain
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Personality Changes, Executive Dysfunction, and Motor and Memory Impairment
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Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
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Paraneoplastic and Autoimmune Encephalitis
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Huntington Disease: Clinical Features and Diagnosis
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A Young Man with Progressive Language Difficulty and Early-Onset Dementia
JAMA Neurol 73:595-599, Botha, H.,et al, 2016
MRI in X-Linked Adrenoleukodystrophy
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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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Prevalence of Cerebral Amyloid Pathology in Persons without Dementia
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Non-Alzheimers Dementia 1 Frontotemporal Dementia
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Non-Alzheimers Dementia 2 Lewy Body Dementias
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Progressive Neuropsychiatric Symptoms and Motor Impairment
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A Case of Early-Onset Rapidly Progressive Dementia
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Disturbances of Cerebrospinal Fluid, Including Hydrocephalus, Pseudotumor Cerebri, and Low-Pressure Syndromes, Normal Pressure Hydrocephalus
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Frontotemporal Dementia
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An Expanded Role for Neuroimaging in the Evaluation of Memory Impairment
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Clinicopath Conf., Adult Cerebral Form of X-Linked Adrenoleukodystrophy
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Association of Parental Dementia With Cognitive and Brain MRI Measures in Middle-Aged Adults
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Frequent Amyloid Deposition Without Significant Cognitive Impairment Among the Elderly
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Sporadic Adult-Onset Leukoencephalopathy with Neuroaxonal Spheroids Mimicking Cerebral MS
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A 34-Year-Old Man With Progressive Behavioral and Language Disturbance
Neurol 68:68-74, Miller,B.L.,et al, 2007
Young-Onset Dementia, A Practical Approach to Diagnosis
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Mild Cognitive Impairment
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CT and MR Imaging of Neuroaxonal Leukodystrophy Presenting as Early-Onset Frontal Dementia
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Dementia and White-Matter Demyelination in Young Patient With Neurosyphilis
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A 32-Year Prospective Study of Change in Body Weight and Incident Dementia
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The Genetic Causes of Basal Ganglia Calcification, Dementia, and Bone Cysts
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Autonomic Failure as the Initial Presentation of Parkinson Disease and Dementia with Lewy Bodies
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