Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995
A 55-Year-Odd Man with Old Behavior and Abnormal Movements
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Clinicopathologic Conference, Pernicious Anemia (Vitamin B12 Deficiency)
NEJM 380:665-674, Case 5-2019, 2019
Personality Changes, Executive Dysfunction, and Motor and Memory Impairment
JAMA Neurol 74:245-246, Lopez Chiriboga, A.S.,et al, 2017
Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
NEJM 375:1879-1890, Case 34-2016, 2016
Neuropsychiatric Changes Precede Classic Motor Symptoms in ALS and Do Not Affect Survival
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Progressive Neuropsychiatric Symptoms and Motor Impairment
JAMA Neurol 71:794-798, Ghadiri, M.,et al, 2014
Anti-N-Methyl-D-Aspartate Receptor (NHMDAR) Encephalitis in Children and Adolescents
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Anti-NMDA-Receptor Encephalitis: Case Series and Analysis of the Effects of Antibodies
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Inborn Errors of Urea Synthesis
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Brain Imaging in Late-Onset CM2 Gangliosidosis
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Psychiatric Disturbances in Metachromatic Leukodystrophy
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Wilson Disease
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Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
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Sarcoidosis of the Nervous System, A Clinical Approach
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Wilson Disease:Clinical Presentation, Treatment, and Survival
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Causalgia and Other Reflex Sympathetic Dystrophies
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Anderson-Fabray Disease, A Commonly Missed Diagnosis
BMJ 297:872-873, Morgan,S.H.&Crawfurd,M., 1988
Neuroaxonal Dystrophy in Young Adults:A Clinicopathological Study of Two Unrelated Cases
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