Neuroradiologic Aspects of Chester-Erdheim Disease
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Trichinosis with Central Nervous System Involvement
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A 35-Year-Old Woman with Personality Change and Gait Impairment
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Neuroimaging Features of Biotinidase Deficiency
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A 48-Year-Old Woman Presenting with Vertigo, Ptosis, and Red Eyes
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A Middle-Aged Man with Progressive Gait Abnormalities
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Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
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Copper Deficiency
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Degenerative Diseases of the Nervous System, Multiple System Atrophy
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Copper Deficiency as a Treatable Cause of Poor Balance
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Cogan Syndrome
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Neurosarcoidosis: A Study of 30 New Cases
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The Hot Cross Bun Sign in the Patients with Spinocerebellar Ataxia
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The Neurological Complications of Bariatric Surgery
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Neurological Complications of Coeliac Disease
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Myelopathy Caused by Nitrous Oxide Toxicity
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Chronic Lymphocytic Leukemia and the Central Nervous System:A clinical and Pathological Study
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Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
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Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
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Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
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Mitochondrial DNA and Disease
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Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
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Tobacco Intolerance in a Habitual Smoker with Cervical Myelopathy
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Spastic Ataxia Associated with Human T-Cell Lymphotropic Virus Type II Infection
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The Pathogenesis of Superficial Siderosis of the Central Nervous System
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Ataxia in epidural Spinal Cord Compression
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Neurologic Aspects of Cobalamin Deficiency
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Sarcoidosis of the Nervous System, A Clinical Approach
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Idiopathic Myelopathies with White Matter Vacuolation in Non-AIDS Patients
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Idiopathic Cerebellar Ataxia of Late Onset:Natural History and MRI Morphology
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Human T-Lymphotropic Virus Type I-Associated Myelopathy Presenting as Spinocerebellar Syndrome
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Clinicopath Conf
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Cogan's Syndrome:18 Cases & a Review of the Literature
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Olivopontocerebellar Atrophy with Dementia, Blindness, & Chorea, Response to Baclofen
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Vacuolar Myelopathy Pathologically Resembling Subacute Combined Degeneration in Patients with AIDS
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Myeloneuropathy & Macrocytosis Associated with Nitrous Oxide Abuse
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Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
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A Family with Hereditary Ataxia:HLA Typing
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Clin. Path. Conference
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Neurologic Disturbances in Pagets Disease of Bone:Response to Calcitonin
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Dominant Spinopontine Atrophy
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Physostigmine in Familial Ataxias
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Spinocerebellar Ataxia & HLA Linkage:Risk Prediction by HLA Typing
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