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Central Nervous System Neuronal Surface Antibody Associated Syndromes: Review and Guidelines for Recognition
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Asymmetric Cerebellar Ataxia and Limbic Encephalitis as a Presenting Feature of Primary Sjogrens Syndrome
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Acute Trimethyltin Limbic-Cerebellar Syndrome
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A 59-Year-Old Man with Progressive Dysarthria and Gait Instability
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Recurrent Rhombencephalitis Associatedwith Anti-GAD65 Antibody
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Supratentorial Lymphocytic Inflammation with Parenchymal Perivascular Enhancement Responsive to Steroids:A Potentially Overlooked Diagnosis
Ann Neurol 95:407-409, Tsibonakis,A.,et al, 2024
Anti-NMDA Receptor Encephalitis Presenting with Cerebellitis in a Pediatric Patient
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A 35-Year-Old Woman with Personality Change and Gait Impairment
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Neuroimaging Features of Biotinidase Deficiency
AJNR 44:328-333, Biswas,A.,et al, 2023
An 82-Year-Old Woman with Subacute Ophthalmoparesis and Ataxia
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A Dizzy Architect
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A 48-Year-Old Woman Presenting with Vertigo, Ptosis, and Red Eyes
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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 16-year-old Girl with Ataxia, Oscillopsia, and Behavioral Changes
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An Adolescent Girl Presenting with Worsening Vertigo, Headache, and Ataxia
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Opsoclonus in Anti-Ma2 Brain-Stem Encephalitis
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A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
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Clinical features, prognostic factors, and antibody effects in anti-mGluR1 encephalitis
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Kelch-Like Protein 11 Antibodies in Seminoma-Associated Paraneoplastic Encephalitis
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Recurrent Dysarthria and Ataxia in a Young Girl
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A 52-year-old woman with a 3 weeks of progressive gait ataxia and dysarthria
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Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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Glial Fibrillary Acidic Protein Immunoglobulin G as Biomarker of Autoimmune Astrocytopathy: Analysis of 102 Patients
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A 73-year-old Man with Diplopia and Ataxia
Neurol 85:e96-e100, Gupta, H.V.,et al, 2015
Central Nervous System Involvement in Whipple Disease
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Anti-Glutamic Acid Decarboxylase Limbic Encephalitis Without Epilepsy Evolving Into Dementia with Cerebellar Ataxia
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Rhombencephalitis A Series of 97 Patients
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Spectrum of Neurological Syndromes Associated with Glutamic Acid Decarboxylase Antibodes: Diagnostic Clues for this Association
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Neuro-Ophthalmologic Manifestations of Paraneoplastic Syndromes
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Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
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Spectrum of Paraneoplastic Neurologic Disorders in Women with Breast and Gynecologic Cancer
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Ataxia Associated with Hashimotos Disease: Progressive Non-Familial Adult Onset Cerebellar Degeneration with Autoimmune Thyroiditis
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Clinicopath Conf, Creutzfeldt-Jakob Disease,Case 28-1999
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Late Onset of Distinct Neurologic Syndromes in Galactosemic Siblings
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Signs & Symptoms from a Cerebral Lesion that Suggest Cerebellar Dysfunction
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