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The Phenotypic Continuum of ATP1A3-Related Disorders
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A 47-year-old Man with Rapidly Progressive Ataxia and Vitiligo
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A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
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An Unusual Fundus Finding in a Teenage Girl
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Extraintestinal Manifestations of Coeliac Disease
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Neuro-Ophthalmologic Manifestations of Paraneoplastic Syndromes
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Cerebellar Ataxia With Anti-Glutamic Acid Decarboxylase Antibodies
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Ataxia Associated with Hashimotos Disease: Progressive Non-Familial Adult Onset Cerebellar Degeneration with Autoimmune Thyroiditis
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Acute Vestibular Syndrome
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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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Familial Hemiplegic Migraine, Nystagmus and Cerebellar Atrophy
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Downbeating Nystagmus
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Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
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Alcoholic Downbeat Nystagmus
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Down-Beat Nystagmus
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Alcoholism
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A 35-Year-Old Woman with Personality Change and Gait Impairment
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Progressive Ataxia and Doenbeat Nystagmus in an Adult
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Early-Onset Head Titubation in a Child with Poretti-Boltshauser Syndrome
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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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Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Whipple Disease
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High Doses of Deferiprone May Be Associated with Cerebellar Syndrome
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Clinical Spectrum of Ataxia-Telangiectasia in Adulthood
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Spectrum of Neurological Syndromes Associated with Glutamic Acid Decarboxylase Antibodes: Diagnostic Clues for this Association
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Asymmetric Cerebellar Ataxia and Limbic Encephalitis as a Presenting Feature of Primary Sjogrens Syndrome
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Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
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Infantile Bilateral Striatal Necrosis Maps to Chromosome 19q
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Nodulus Infarction Mimicking Acute Peripheral Vestibulopathy
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Autoantibodies to Glutamic Acid Decarboxylase in Downbeat Nystagmus
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Cerebral Manifestation of Erdheim-Chester Disease:Clinical and Radiologic Findings
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
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Central Nervous System Involvement in Von Hippel-Lindau Disease
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Craniopharyngyoma in Children
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