Clinicopathologic Conference, Creutzfeldt-Jakob Disease
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Wernekink Commissure Syndrome Secondary to Bilateral Caudal Paramedian Midbrain Infarction Presenting with a Unique "Heart or V" Appearance Sign:Case Report and Review of the Literature
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The Autosomal Recessive Cerebellar Ataxias
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A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
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A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
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An 82-Year-Old Woman with Subacute Ophthalmoparesis and Ataxia
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Wernekinck Commissure Syndrome
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A Dizzy Architect
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A 37-Year-Old Man with Involuntary Movements, Gait Disturbance, and Hyperasthesia
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More Than a Little Unsteady
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The Phenotypic Continuum of ATP1A3-Related Disorders
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Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
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A 47-year-old Man with Rapidly Progressive Ataxia and Vitiligo
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Complex Ataxia
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A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
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A 60-year-old woman with ataxia
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Early-Onset Head Titubation in a Child with Poretti-Boltshauser Syndrome
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A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
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Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Whipple Disease
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Clinicopathologic Conference, Acute Infectious Mononucleosis due to Epstein-Barr Virus Infection, Complicated by Acute Otitis Media and Postinfectious Cerebellitis
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Central Nervous System Involvement in Whipple Disease
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Slurred Speech and Spirochaetes
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Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
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West Nile Virus Presenting as Opsoclonus-myoclonus Cerebellar Ataxia
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Recessive Ataxia With Ocular Apraxia
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Cerebellar Degeneration Associated With Human Immunodeficiency Virus Infection
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Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
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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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Cerebellar Symptoms as Presenting Manifest of Bilirubin Encephal in Children with Crigler-Najjar Type I Disease
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
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Adult Celiac Disease Presenting as Cerebellar Syndrome
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Nervous System Toxicity of Chemo Agents
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Neurologic Abnormalities of Lyme Disease
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Kearns-Sayre Syndrome with Hypoparathyroidism
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Ocular Motor Abnormalities in Hereditary Cerebellar Ataxia
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Neurological Problems in Endocrine Diseases
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Genetic Counseling in Retinitis Pigmentosa
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An Acute Syndrome of Ocular Oscillations & Truncal Ataxis
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