Cognitive and Clinical Characteristics of Patients with Limbic-Predominant Age-Related TDP-43 Encephalopathy
Neurol 100:e2027-e2035, Pagnotti,R.M.B.,et al, 2023
Sport Associated Dementia
BMJ 372:N168, Stewart, W., 2021
Single Photon Emission Computed Tomography/Positron Emission Tomography Molecular Imaging for Parkinsonism: A Fast-Developing Field
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Clinicopathologic conference, Frontotemporal Lobar Degeneration with tau-positive inclusions consistent with Picks disease
NEJM 383:2666-2675, Case 41-2020, 2020
Stridor in Multiple System Atrophy
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Neurodegenerative Disease Mortality Among Former Professional Soccer Players
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Atypical Parkinsonian Syndromes: A General Neurologists Perspective
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Pantothenate Kinase - Associated Neurodegeneration (PKAN)
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Clinicopathologic Conference, Primary Progressive Aphasia, Semantic Variant, due to TAR DNA Binding Protein 43 associated Frontotemporal Lobar Degen
NEJM 376:158-167, Case 1-2017, 2017
Amyotrophic Lateral Sclerosis
NEJM 377:162-172, Brown, R.H.,et al, 2017
Dentate Update: Imaging Features of Entities that Affect the Dentate Nucleus
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Neuroimaging Changes in Menkes Disease, Part 1
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A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
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A Young Man with Progressive Language Difficulty and Early-Onset Dementia
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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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Criteria for the Diagnosis of Corticobasal Degeneration
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Clinical Reasoning: A Woman with Rapidly Progressive Apraxia
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Ataxia, Dementia, and Hypogonadotropism Caused by Disordered Ubiquitination
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Neurodegenerative causes of death among retired National Football League Players
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Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
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Skin biopsy is useful for the antemortem diagnosis of neuronal intranuclear inclusion disease
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The Spectrum of Mutations in Progranulin: A Collaborative Study Screening 545 Cases of Neurodegeneration
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Huntingtons Disease
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Rapidly Progressive Neurodegenerative Dementias
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Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
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Progressive Supranuclear Palsy: A Current Review
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Spinal Muscular Atrophy
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Rapidly Progressive Dementia
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Neuroimaging Findings in Human Prion Disease
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Amyotrophic Lateral Sclerosis
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Palliative Care for Patients With Amyotrophic Lateral Sclerosis
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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Alzheimer's Disease and Parkinson's Disease
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The Topography of Metabolic Deficits in Posterior Cortical Atrophy (the Visual Variant of Alzheimers Disease) with FDG-PET
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Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
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Recessive Ataxia With Ocular Apraxia
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CSF Detection of the 14-3-3 Protein in Unselected Patients with Dementia
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Positron Emission Tomography in Evaluation of Dementia
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A New Metabolite Contributing to N-Acetyl Signal in 1H MRS of the Brain in Salla Disease
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Frontotemporal Degeneration, Pick Disease, and Corticobasal Degeneration
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Frontotemporal Dementia, Pick Disease, and Corticobasal Degeneration
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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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A New Variant of Creutzfeldt-Jakob Disease in the UK
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Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
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Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
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Medical Aspects of the Persistent Vegetative State
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The Apolipoprotein E Alleles as Major Susceptibility Factors for Creutzfeldt-Jakob Disease
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