Clinicopathologic conference, Malignant Mixed Germ-Cell Tumor and Anti-NMDA Receptor Encephalitis
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Niemann-Pick Type C Disease
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A 68-YEar-Old Man with Progressive Numbness, Vertigo, and Cognitive Decline
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Niemann-Pick Disease Type C
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A 35-Year-Old Woman with Personality Change and Gait Impairment
Neurol 104:e210252, Bernardes,C.,et al, 2024
Clinicopathologic Conference, Functional Vitamin B12 Deficiency from Use of Nitrous Oxide
NEJM 388:1893-1900, Case 15-2023, 2023
Neuroimaging Biomarkers in a Patient with Probable Psychiatric-Onset Prodromal Dementia with Lewy Bodies
Neurol 99:654-657, Urso, D.,et al, 2022
The Phenotypic Continuum of ATP1A3-Related Disorders
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Sporadic Creutzfeldt-Jakob Disease in a Very Young Person
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A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
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Neurosyphilis
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Antibody-Mediated Encephalitis
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Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
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Intrathecal 2-hydroxypropyl-�-cyclodextrin Decreases Neurological Disease Progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial
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Adult-Onset Niemann-Pick Disease Type C: Rapid Treatment Initiation Advised but Early Diagnosis Remains Difficult
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Cognitive Impairment Profile in adult Patients with Neimnn Pick Type C Disease
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Paraneoplastic Cerebellar Degeneration with Anti-Yo Antibodies - A Review
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Kleine-Levin Syndrome in 120 Patients: Differential Diagnosis and Long Episodes
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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
NEJM 372:1151-1162, Miller, B.L.,et al, 2015
Non-Alzheimers Dementia 1 Frontotemporal Dementia
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Neuropsychiatric Changes Precede Classic Motor Symptoms in ALS and Do Not Affect Survival
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Progressive Neuropsychiatric Symptoms and Motor Impairment
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Psychosis in an Adolescent Girl: A Common Manifestation in Niemann-Pick Type C Disease
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Frontotemporal Dementia
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Diagnosing variant Creutzfeldt-Jakob disease: a retrospective analysis of the first 150 cases in the UK
JNNP 82:646-651, Heath, C.A.,et al, 2011
Anti-N-Methyl-D-Aspartate Receptor (NHMDAR) Encephalitis in Children and Adolescents
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The Alcohol Withdrawal Syndrome
JNNP 79:854-862, McKeon,A.,et al., 2008
Anti-NMDA-Receptor Encephalitis: Case Series and Analysis of the Effects of Antibodies
Lancet Neurol 7:1091-1098, Dalmau,J.,et al, 2008
Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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Mental Illness in New Neurological Patients
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Clinical Features and Neuropathology of Autosomal Dominant Spinocerebellar Ataxia (SCA17)
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Neurological Complications of Coeliac Disease
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Avoiding Pitfalls in the Diagnosis of Subarachnoid Hemorrhage
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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
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Hashimoto's Encephalitis as a Differential Diagnosis of Creutzfeldt-Jakob Disease
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Retinocochleocerebral Vasculopathy
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Susac Syndrome
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Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms
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Subcotical Arteriosclerotic Encephalopathy (Binswangers Disease)
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Hereditary Frontotemporal Dementia is Linked to Chromosome 17q21-q22:Genetic & Clinicopath Study of 3 Dutch Families
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Comparison of Extrapyramidal Features in 31 Path Cases of Diffuse Lewy Body Disease & 34 Cases of Parkinson's
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New Variant Creutzfeldt-Jakob Disease:Neurological Features and Diagnostic Tests
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BSE Linked to New Variant of CJD in Humans
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A New Variant of Creutzfeldt-Jakob Disease in the UK
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Neuropsychiatric Aspects of Progressive Supranuclear Palsy
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Diagnostic Guidelines in Central Nervous System Whipple's Disease
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Nonmotor Fluctuations in Patients with Parkinson's Disease
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Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
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Mitochondrial DNA and Disease
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