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A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
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Unmasking Cerebrotendinous Xanthomatosis, Clinical Recognition of a Treatable Cause of Progressive Ataxia
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A 24-Year-Old Man with Spastic Ataxia and Hypodontia
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A 26-Year-Old Woman with Chronic Progressive Gait Dysfunction
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Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
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A Middle-aged Woman with Severe Scoliosis and Encephalopathy
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A 25-year-old Woman with Recurrent Episodes of Collapse and Loss of Consciousness
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Ears of the Lynx Magnetic Resonance Imaging Sign
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Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
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Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
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A Neonate with Micrognathia and Hypotonia
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The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
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Familial Idiopathic Striopallidodentate Calcifications
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Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
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Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
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Familial Spastic Paraplg, Peroneal Neuropathy, & Crural Hypopig, A New Neurocut Synd
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Progressive Spastic Paraparesis & Adrenal Insufficiency
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Systematic Genetic Assessment in Young Patients with Cryptogenic Stroke: The ES-EASY Project
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Niemann-Pick Type C Disease
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Ribbon-Like Sign in Convexity Subarachnoid Hemorrhage
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A 60-Year-Old Man with Weakness and Gait Dysfunction
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Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
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Adult-Onset Coats Plus, A Case of Leukoencephalopathy with Calcifications, a Tumefactive Brain Lesion, and a Presumed Autoimmune Disease
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A 10-Year-Old Boy with Progressive Tremor, Insomnia and Autonomic Dysfunction
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Multivessel Cerebral Occlusion in Noonan Syndrome
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A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
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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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A 50-YEar-Old Man with Intracerebral Hemorrhage and Tortuous Retinal Arterioles
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A 35-Year-Old Woman with Personality Change and Gait Impairment
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RNF213 Polymorphisms in Intracranial Artery Dissection
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A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
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A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
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Neonatal Seizures
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Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy
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A 48-Year-Old Man With Spasticity and Progressive Ataxia
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Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
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Leber Hereditary Optic Neuropathy with Longitudinal Spinal Cord Lesion Mimicking Spinal Cord Infarction
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Unilateral Leukoencephalopathy Revealing Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
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