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Reversible Cortical and Basal Ganglia Lesions in Late-Onset Methylmalonic Aciduria
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Roving Eye and Head in a Patient with Genetic Creutzfeldt-Jakob Disease
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Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
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Pomalidomide for Epistaxis in Hereditary Hemorrhagic Telangiectasia
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Comparative Effects of Drug Interventions for the Acute Management of Migraine Episodes in Adults:Systematic Review and Network Meta-Analysis
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Newborn Screening and Presymptomatic Treatment of Metachromatic Leukodystrophy
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Lentiviral Gene Therapy for Cerebral adrenoleukodystrophy
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A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
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A 65-Year-Old Woman with Isolated Macroglossia as the Initial Presentation of a Rare Disease
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Genome Sequencing in the NICU and PICU is Here to Stay
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Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia
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Focusing on the Eye Signs of Alport Syndrome in a 40-Year-Old Man Who Previously Had a Kidney Transplant and Hearing Loss
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Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
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Neuroimaging Features of Biotinidase Deficiency
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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
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Paroxysmal Exercise-Induced Dyskinesias Due to Pyruvate Dehydrogenase Deficiency
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Atogepant for the Preventive Treatment of Chronic Migraine (PROGRESS): A Randomised, Double-blind, Placebo-controlled, Phase 3 Trial
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Movement Disorders in Patients with Genetic Developmental and Epileptic Encephalopathies
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Hereditary Hemorrhagic Telangiectasia, Clinical Presentations, and Management
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Brain Tumors in Children
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Unilateral Leukoencephalopathy Revealing Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
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Bilateral Hearing Loss and Constricted Visual Fields
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Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction
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