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CSF Tests in the Differential Diagnosis of Cretuzfeldt-Jakob Disease
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Plasma Exchange in Neuroimmunological Disorders: Part 2. Treatment of Neuromuscular Disorders
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Collaborative Analysis of a-Synuclein Gene Promotor Variability and Parkinson Disease
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Restless Legs Syndrome: Is Treatable But Under-Recognised
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Frontotemporal Dementia: Clinicopathological Correlations
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Finding the Causes of Inherited Neuropathies
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Parkinsons Disease and Genetics
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Multiple Sclerosis with and without CSF Bands:Clinically Indistinguishable but Immunogenetically Distinct
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The Tuberous Sclerosis Complex
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Familial Cervical Artery Dissections: Clinical, Morphologic, and Genetic Studies
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Case 35-2006: A Newborn Boy with Hypotonia
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Genetics of Parkinsons Disease and Parkinsonism
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Prognosis of Migraine Headaches in Adolescents: A 10-Year Follow-Up Study
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CSF Findings in 250 Patients with Serologically Confirmed West Nile Virus Meningitis and Encephalitis
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Multiple Diagnostic Tests Are Needed to Assess Multiple Causes of Dementia
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Prevalence of Fabry Disease in Patients with Cryptogenic Stroke: A Prospective Study
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Clinically Isolated Syndromes, A New Oligoclonal Band Test Accurately Predicts Conversion to MS
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Familial Dopa-Responsive Cervical Dystonia
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Metabolic Disease and Stroke: MELAS
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Benign Tremulous Parkinsonism
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Role of COL4A1 in Small-Vessel Disease and Hemorrhagic Stroke
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Frontotemporal Lobar Degeneration with Motor Neuron Disease
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Poststroke C-Reactive Protein Is a Powerful Prognostic Tool Among Candidates for Thrombolysis
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Neuropathologic Features of Amnestic Mild Cognitive Impairment
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Spontaneous Spinal Cerebrospinal Fluid Leaks and Intracranial Hypotension
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Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
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Mitochondrial DNA Polymerase-y and Human Disease
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Concomitant Chronic Inflammatory Demyelinating Polyneuropathy and Myasthenia Gravis Following Cytomegalovirus Infection
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Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects
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Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
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Unusual Presentation of Central Nervous System Cryptococcal Infection in an Immunocompetent Patient
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Update on Susacs Syndrome
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Spectrum of Mutations in Biopsy-Proven CADASIL: Implications for Diagnostic Strategies
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Heritability of Carotid Artery Atherosclerotic Lesions
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Science and Ethics of Sham Surgery, A Survey of Parkinson Disease Clinical Researchers
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Protein S Deficiency in HIV Associated Ischaemic Stroke:An Epiphenomenon of HIV Infection
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Evaluation of C-Reactive Protein Measurement for Assessing the Risk and Prognosis in Ischemic Stroke
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Neuroblastoma -- from Genetic Profiles to Clinical Challenge
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Brain Magnetic Resonance Imaging in Patients with Cowden Syndrome
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Psychosocial Impact of Screening for Intracranial Aneurysms in Relatives with Familial Subarachnoid Hemorrhage
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The Clinical and Genetic Spectrum of Spinocerebellar Ataxia 14
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