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A 51-Year-Old Woman with Abnormal Corups Callosum Signal
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A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
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Thyrotoxic Periodic Paralysis
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Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
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A 59-Year-Old Man with Progressive Proximal Weakness Since Childhood
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A 54-year-old man with Dyspnea and Muscle Weakness
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A Teenager with Persistent Headache
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Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
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Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases
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FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
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Sudden-Onset Pulsatile Headache in a Previously Healthy Young Man
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Personality Changes, Executive Dysfunction, and Motor and Memory Impairment
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A 13-year-old boy with Chronic Ataxia and Developmental Delay
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Choreoathetosis, Dystonia, and Myoclonus in 3 Siblings with Autosomal Recessive Spinocerebellar Ataxia Type 16
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Paroxysmal Kinesigenic Dyskinesia
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Chronic and Slowly Progressive Weakness of the Legs and Hands
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Red Papules on the Tongue of a Patient with Hemiparesis
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A 52-year-old Woman with Progressive Proximal Weakness
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Inherited Metabolic Diseases of the Nervous System, Hepatolenticular Degeneration (Wilson Disease)
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Extending the KCNQ2 encephalopathy Spectrum
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Clinical and Biomarker Changes in Dominantly Inherited Alzheimers Disease
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Genetic Aspects of Alzheimer Disease
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Spinal Muscular Atrophy
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Biochemical Markers in Persons With Preclinical Familial Alzheimer Disease
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Wilson Disease: Description of 282 Patients Evaluated Over 3 Decades
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Identification of New Presenilin Gene Mutations in Early-Onset Familial Alzheimer Disease
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Familial Infantile Bilateral Striatal Necrosis
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Hereditary Benign Chorea
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Association Between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene
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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
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Serial Magnetic Resonance Imaging of Cerebral Atrophy in Preclinical Alzheimer's Disease
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Rapid-Onset Dystonia-Parkinsonism:Linkage to Chromosome 19q13
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