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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
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A 77-Year-Old Man with Involuntary Movements, Sleep Changes, Falls, Bulbar Symptoms, and Cognitive Complaints
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The Phenotypic Continuum of ATP1A3-Related Disorders
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Duchenne Muscular Dystrophy
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Progressive Multifocal Leukoencephalopathy: Epidemiology, Clinical Manifestations, and Diagnosis
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Advances in Progressive Supranuclear Palsy: New Diagnostic Criteria, Biomarkers, and Therapeutic Approaches
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Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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Disturbances of Cerebrospinal Fluid, Including Hydrocephalus, Pseudotumor Cerebri, and Low-Pressure Syndromes, Normal Pressure Hydrocephalus
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Intracranial Neoplasms and Paraneoplastic Disorders, Hemangioblastoma of the Cerebellum
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Paraneoplastic Neurological Syndromes
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The Limbic-Girdle Muscular Dystrophies
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Rhombencephalitis A Series of 97 Patients
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Assessment: Symptomatic Treatment for Muscle Cramps (an Evidence-Based Review): Report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology
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Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
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Progressive Supranuclear Palsy: A Current Review
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Spectrum of Neurological Syndromes Associated with Glutamic Acid Decarboxylase Antibodes: Diagnostic Clues for this Association
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Spinal dural arteriovenous fistulas: a congestive myelopathy that initially mimics a peripheral nerve disorder
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Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects
Lancet Neurol 4:239-248, Shahwan, A., et al, 2005
Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
NEJM 348:33-40, Hayflick,S.J.,et al, 2003
Mitochondrial Respiratory-Chain Diseases
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The Hereditary Spastic Paraplegias
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Glutamic Acid Decarboxylase Autoantibodies and Neurological Disorders
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Cardiac Dysfunction in Neuromuscular Diseases
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The Clinical Spectrum of Anti-GAD Antibody-Positive Patients with Stiff-Person Syndrome
Neurol 55:1531-1535, Dalakas,M.C.,et al, 2000
Paraneoplastic Syndromes
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Molecular Basis of the Neurodegenerative Disorders
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Neurologic Complications in Children with Enterovirus 71 Infection
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Retinocochleocerebral Vasculopathy
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Neurologic Aspects of Inflammatory Bowel Disease
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The Prevention of Neurogenetic Disease
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Mitochondrial DNA and Disease
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Trinucleotide Repeat Expansion in Neurological Disease
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Molecular Genetics in Neurology
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Sarcoidosis of the Nervous System, A Clinical Approach
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Retinitis Pigmentosa
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Progressive Multifocal Leukoencephalopathy Associated with Human Immunodeficiency Virus Infection
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The Clinical Features & Natural History of the Steele-Richardson-Olszewski Syndrome (Prog Supranuclear Palsy)
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Wernicke's Encephalopathy
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Unveiling the Clinical and Imaging Signatures of Intravascular Lymphoma of the Central Nervous System:A Multicentric Cohort Study
Ann Neurol 97:435-448, Berthet,E.,et al, 2025
Behcets Syndrome
NEJM 390:640-651, Saadoun,D.,et al, 2024
Parkinsons Disease
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Primary Central Nervous System Vasculitis
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Neuroimaging Features of Biotinidase Deficiency
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