The Phenotypic Continuum of ATP1A3-Related Disorders
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Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
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Ependymomas of the Posterior Cranial Fossa:CT and MRI Findings
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A Dizzy Architect
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Palatal Myoclonus, Abnormal Eye Movements, and Olivary Hypertrophy in GAD65-Related Disorder
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A 16-year-old Girl with Ataxia, Oscillopsia, and Behavioral Changes
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A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
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Clnicopathologic Conference Anti-N-Methyl-D-Aspartate (NMDA) Receptor Encephalitis
NEJM 379:870-878, CASE 27-2018, 2018
Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
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Pyruvate Dehydrogenase Deficiency (PDCD)
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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Clinical Manifestations of the anti-IgLON5 Disease
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Inherited Metabolic Diseases of the Nervous System, Subacute Necrotizing Encephalopathy (Leigh Disease)
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Central Nervous System Neuronal Surface Antibody Associated Syndromes: Review and Guidelines for Recognition
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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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Clinical Spectrum of Ataxia-Telangiectasia in Adulthood
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Neuro-Ophthalmologic Manifestations of Paraneoplastic Syndromes
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Asymmetric Cerebellar Ataxia and Limbic Encephalitis as a Presenting Feature of Primary Sjogrens Syndrome
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Age and High-Dose Methotrexate are Associated to Clinical Acute Encephalopathy in FRALLE 93 Trial for Acute Lymphoblastic Leukemia in Children
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Spectrum of Paraneoplastic Neurologic Disorders in Women with Breast and Gynecologic Cancer
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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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Mitochondrial DNA and Disease
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Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Self-Limited Granulomatous Angiitis of the Cerebellum
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Neurologic Disturbances in Pagets Disease of Bone:Response to Calcitonin
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Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
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A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
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A 59-Year-Old Man with Progressive Dysarthria and Gait Instability
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Clinicopathological Conference, Powasan Virus Encephalitis
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The Spectrum of Fragile X Disorders
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A 63-Year-Old Female Patient Presenting with Orthostatic Hypotension and Ataxia
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Unmasking Cerebrotendinous Xanthomatosis, Clinical Recognition of a Treatable Cause of Progressive Ataxia
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A 59-Year-Old Female Patient with Urinary Dysfunction and Lightheadedness
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A 30-Year-Old Female Patient with Multiple Sclerosis Presenting with Rapidly Progressive Cranial Neuropathies, Weakness, and Ataxia
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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
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Anti-NMDA Receptor Encephalitis Presenting with Cerebellitis in a Pediatric Patient
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Diffusely Enhancing Lesions on MRI in DPPX Antibody-Associated Encephalitis
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A 24-Year-Old Man with Spastic Ataxia and Hypodontia
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Expanding Clinical Spectrum an Anti-GQ1b Antibody Syndrome, A Review
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A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
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A 35-Year-Old Woman with Personality Change and Gait Impairment
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Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
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Occult Breast Cancer with Anti-Ri Antibody Positivity and Pontine Hot Cross Bun Sign
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Neuroimaging Features of Biotinidase Deficiency
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