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A 51-Year-Old Woman with Abnormal Corups Callosum Signal
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A 42-year-old Woman with Progressive Cognitive Difficulties and Gait Imbalance
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Spinal Cord Involvement in Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia
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Personality Changes, Executive Dysfunction, and Motor and Memory Impairment
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Inherited Metabolic Diseases of the Nervous System, Neuroaxonal Dystrophy
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Progressive Neuropsychiatric Symptoms and Motor Impairment
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Clinical Reasoning: A Woman with Rapidly Progressive Apraxia
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T2* and FSE MRI Distinguishes Four Subtypes of Neurodegeneration With Brain Iron Accumulation
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Insights into the Dynamics of Hereditary Diffuse Leukoencephalopathy with Axonal Spheroids
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Sporadic Adult-Onset Leukoencephalopathy with Neuroaxonal Spheroids Mimicking Cerebral MS
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What Do We Really See When We Look at Magnetic Resonance Images?
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CT and MR Imaging of Neuroaxonal Leukodystrophy Presenting as Early-Onset Frontal Dementia
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Autosomal Dominant Diffuse Leukoencephalopathy with Neuroaxonal Spheroids
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Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria
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Axonal Transection in the Lesions of Multiple Sclerosis
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The Prevention of Neurogenetic Disease
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Trinucleotide Repeat Expansion in Neurological Disease
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Molecular Genetics in Neurology
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The Polymerase Chain Reaction:Application to Nervous System Disease
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The Use of Magnetic Resonance Imaging in Diagnosing Infantile Neuroaxonal Dystrophy
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Stroke-Like Syndrome, Mineralizing Microangiopathy, and Neuroaxonal Dyst with Intrathecal Methotrexate
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Neuroaxonal Dystrophy Due to Lysosomal a-N-Acetylgalactosaminidase Deficiency
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Mineralization of the Basal Ganglia Detected by CT in Hallervorden-Spatz Syndrome
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The Molecular Genetic Revolution, Its Impact on Clinical Neurology
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Genetic Linkage in Neurologic Diseases
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Examination of Dental Pulp to Diagnose Infantile Neuroaxonal Dystrophy
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Acute Thallium Poisoning, Toxicological & Morphological Studies of the Nervous System
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A Progressive Neurologic Syndrome In Children With Chronic Liver Disease
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An Ultramicroscopic Study of Skin & Conjunctival Biopsies in Chronic Neuro. Disorders of Childhood
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Diagnosis of Infatile Neuroaxonal Dystrophy by Skin Biopsy
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Weakness in Malignancy:Evidence for a Remote Effect of Tumor on Distal Axons
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A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
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Cancer Risk in Patients with Muscular Dystrophy and Myotonic Dystrophy
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Supratentorial Lymphocytic Inflammation with Parenchymal Perivascular Enhancement Responsive to Steroids:A Potentially Overlooked Diagnosis
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A 60-Year Old Man with Asymmetric Weakness and Persistent Fever
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Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy
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A Woman with Progressive Painless Sequential Monocular Vision Loss
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Miller Fisher Syndrome and Acute Motor and Sensory Axonal Neuropathy (AMSAN) Variant Guillain-Barre Overlap Syndrome (MFS/AMSAN-GBS) After Upper Respiratory Tract Infection (URTI)
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Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
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Rituximab Therapy in the Treatment of Juvenile Myasthenia Gravis
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Bilateral Hearing Loss and Constricted Visual Fields
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Clinicopathologic Conference, Systemic Juvenile Idiopathic Arthritis
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A 28-Year-Old Woman with Vision Loss and an Unusual Gait
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A 6-Year-Old Boy with Muscle Twitching
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Complete Evaluation of Dementia: PET and MRI Correlation and Diagnosis for the Neuroradiologist
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