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Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
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Multiple Subpial Transection:A Review of 21 Cases
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Epidural Air From Bronchopleural-Epidural-Cutaneous Fistula Producing Reversible Myelopathy and Radiculopathy Symptoms
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Growth Factors:Potential Therapeutic Applications in Neurology
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A Plasma Exchange Versus Immune Globulin Infusion Trial in Chronic Inflammatory Demyelinating Polyradiculoneuropathy
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Preliminary NINDS Neuropathologic Criteria for Steele-Richardson-Olszewski Syndrome (Progressive Supranuclear Palsy)
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Brief Report:Diagnosis of Whipple's Disease by Molecular Analysis of Peripheral Blood
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Mutation Analysis in Patients with Possible but Apparently Sporadic Huntington's Disease
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Progressive Spastic Paraparesis Revealing Primary Hyperparathyroidism
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Trinucleotide Repeat Expansion in Neurological Disease
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Neurologic Manifestations of HIV Infection
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Clinicopathologic Correlations of HIV-1-Associated Vacuolar Myelopathy:An Autopsy-Based Case-Control Study
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Polymerase Chain Reaction and the Diagnosis of Viral Central Nervous System Diseases
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Guidelines for the Management of Aneurysmal Subarachnoid Hemorrhage
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Imaging in Acute Basilar Artery Thrombosis
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Diagnosis of Moyamoya Disease with Magnetic Resonance Angiography
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A Controlled Trial of Riluzole in Amyotrophic Lateral Sclerosis
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Conjugal Amyotrophic Lateral Sclerosis:A Report on Two Couples from Southern France
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Advances in Molecular Analysis of Fragile X Syndrome
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Speculations on Antineuronal Antibody-Mediated Neuropsychiatric Disorders of Childhood
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A Randomized Trial of Test Result Sequencing in Patients with Suspected Multiple Sclerosis
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Plasma Exchange and Intravenous Immunoglobulin Treatment of Neuromuscular Disease
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Herpes Simplex Type 2 in a Patient with Mollaret's Meningitis:Demonstration by Polymerase Chain Reaction
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Anti-Hu-Associated Peripheral Nerve and Muscle Microvasculitis
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Ocular Myasthenia:A Protean Disorder
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Intensive Care of Acute Guillain-Barre Syndrome
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Neurocysticercosis in Houston, Texas:A Report of 112 Cases
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Cerebrotendinous Xanthomatosis:Molecular Diagnosis Enables Presymptomatic Detection of a Treatable Disease
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Congential Deficienty of Factor VII in Subarachnoid Hemorrhage
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