Neurological Problems in Endocrine Diseases
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A 48-Year-Old Man With Spasticity and Progressive Ataxia
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Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
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The Autosomal Recessive Cerebellar Ataxias
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Asymmetric Cerebellar Ataxia and Limbic Encephalitis as a Presenting Feature of Primary Sjogrens Syndrome
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Neurology of Ciguatera
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Paraneoplastic Cerebellar Degeneration
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Movement Disorders in Alcoholism:A Review
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A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
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Wernekinck Commissure Syndrome
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More Than a Little Unsteady
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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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Complex Ataxia
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Clinical features, prognostic factors, and antibody effects in anti-mGluR1 encephalitis
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Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
Neurol 92:101-103, Kang, M.J.,et al, 2019
Stridor in Multiple System Atrophy
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Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019
Clinical Presentation and Cranial MRI Findings of Listeria Monocytogenes Encephalitis
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Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
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Early-Onset Head Titubation in a Child with Poretti-Boltshauser Syndrome
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A 27-year-old man with Acute-Onset Ataxia
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A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017
A 54-year-old woman with Dementia, Myoclonus, and Ataxia
Neurol 89:e7-e12, Ali, F.,et al, 2017
Intrathecal 2-hydroxypropyl-�-cyclodextrin Decreases Neurological Disease Progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial
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Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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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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Intracranial Neoplasms and Paraneoplastic Disorders, Hemangioblastoma of the Cerebellum
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Degenerative Diseases of the Nervous System, Cerebellar Degeneration
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Central Nervous System Involvement in Whipple Disease
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Mycoplasma Pneumoniae Infection: Neurologic Complications
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Central Nervous System Neuronal Surface Antibody Associated Syndromes: Review and Guidelines for Recognition
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Heterogeneity of Coenzyme Q10 Deficiency
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Epstein-Barr Virus Infections of the Nervous System
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Clinical Spectrum of Ataxia-Telangiectasia in Adulthood
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The Hot Cross Bun Sign in the Patients with Spinocerebellar Ataxia
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Second Consensus Statement on the Diagnosis of Multiple System Atrophy
Neurol 71:670-676, Gilman,S.,et al., 2008
Spectrum of Neurological Syndromes Associated with Glutamic Acid Decarboxylase Antibodes: Diagnostic Clues for this Association
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Superficial Siderosis
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Causative Factors and Epidemiology of Bilateral Vestibulopathy in 255 Patients
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Penetrance of the Fragile X-Associated Tremor/Ataxia Syndrome in a Premutation Carrier Population
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Glutamic Acid Decarboxylase Autoantibodies and Neurological Disorders
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Brainstem Gliomas in Adults: Prognostic Factors and Classification
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Ataxia Associated with Hashimotos Disease: Progressive Non-Familial Adult Onset Cerebellar Degeneration with Autoimmune Thyroiditis
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Paraneoplastic Syndromes
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Chronic Lymphocytic Leukemia and the Central Nervous System:A clinical and Pathological Study
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Clinicopathological Study of 35 Cases of Multiple System Atrophy
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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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