Recurrent Rhombencephalitis Associatedwith Anti-GAD65 Antibody
Neurol 102:e208040, Alferes,A.R.,et al, 2024
Supratentorial Lymphocytic Inflammation with Parenchymal Perivascular Enhancement Responsive to Steroids:A Potentially Overlooked Diagnosis
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Clinicopathologic Conference, Anti-IgLON5 IgG-Associated Neurologic Disorder
NEJM 386:173-180, Case 1-2022, 2022
A 55-Year-Old Woman with Recurrent Episodes of Aphasia and Vision Changes
Neurol 98:330-335, Jeanneret, V.,et al, 2022
Pernicious Anaemia
BMJ 369:m1319, Mohamed, M.,et al, 2020
Strokelike Episodes in a Patient with Chronic Gait Abnormalities
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When MRI is a Clue in Episodic Ataxia
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Paraoxysmal Tonic Upgaze in Children, Three Case Reports and a Review of the Literature
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Recurrent Dysarthria and Ataxia in a Young Girl
JAMA Neurol 75:125-126, Romba, M.,et al, 2018
Persistent Postural-Perceptual Dizziness (PPPD): A Common, Characteristic and Treatable Cause of Chronic Dizziness
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Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
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Inherited Metabolic Diseases of the Nervous System, Subacute Necrotizing Encephalopathy (Leigh Disease)
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Degenerative Diseases of the Nervous System, Friedreich Ataxia
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A 72-year-old Man with Rapid Cognitive Decline and Unilateral Muscle Jerks
Neurol 82:e194-e197, Duncan, M.,et al, 2014
Recognition and Management of Withdrawal Delirium
NEJM 371:2109-2113, Schuckit, M.A., 2014
Multimodal Imaging of Reversible Cerebral Vasoconstriction Syndrome: A Series of 6 Cases
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GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
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Epstein-Barr Virus Infections of the Nervous System
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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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Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
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Clinical Spectrum of Episodic Ataxia Type 2
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Headache and CNS White Matter Abnormalities Associated with Gluten Sensitivity
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Cardiac Dysfunction in Neuromuscular Diseases
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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
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Rotational Vertebral Artery Occlusion Syndrome with Vertigo Due to "Labyrinthine Excitation"
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Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
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Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms
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Neurological Channelopathies, Dysfunctional Ion Channels May Cause Many Neurological Diseases
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Calcium Channels in Neurological Disease
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Spinocerebellar Ataxia Type 6, Frequency of the Mutation & Genotype-Phenotype Correl
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Familial episodic Ataxia:Clinical Heterogeneity in Four Families Linked to Chromosome 19p
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Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
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Infarction in the Anterior Rostral Cerebellum (the Territory of the Lateral Branch of the Superior Cerebellar Artery)
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Acetazolamide-Responsive Vestibulocerebellar Syndrome:Clinical & Oculographic Features
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Refsum Disease
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Magnetic Resonance Imaging in Familial Paroxysmal Ataxia
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The Leaking Labyrinth
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Neuro-Ophthalmologic Findings in Vestibulocerebellar Ataxia
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Relapsing Ophthalmoparesis-Sensory Neuropathy Syndrome
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Acetazolamide-Responsive Episodic Ataxia Syndrome
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Complications of Intravenous Phenytoin for Acute Treatment of Seizures
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Paroxysmal Symptoms as the First Manifestations of Multiple Sclerosis
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Familial Periodic Ataxia
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Hereditary Paroxysmal Ataxia:Response to Acetazolamide
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Reversible Corticospinal Tract Disease Due to Hyperthyrodisim
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