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Stroke 4:958, Greenlee,J.E.,et al, 1973
Genetic Counseling in Retinitis Pigmentosa
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Tapping-Triggered Seizure Secondary to Focal Cortical Dysplasia in the Primary Somatosensory Cortex
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Melas Syndrome
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Behcets Syndrome
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Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD): Clinical Features and Diagnosis
UptoDate.com, March, Flanagan,E.P. & Tillema,J-M, 2023
Posterior Reversible Encephalopathy Syndrome
NEJM 388:2171-2178, Geocadin,R.G., 2023
Neurologic Complications of Babesiosis, United States, 2011-2021
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Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD):Clinical Features and Diagnosis
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Diagnosis of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease:International MOGAD Panel Proposed Criteria
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Multiple Cranial Nerve Gadolinium Enhancement in Norrie Disease
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Updates on Sturge-Weber Syndrome
Stroke 53:3769-3779, Yeom,S.E.&Comi,A.M., 2022
Sturge-Weber Syndrome
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Congenital Cytomegalovirus Infection
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Clinical and Neuroimaging Findings in MOGAD-MRI and OCT
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Pyogenic Brain Abscesses in a Patient with Digital Clubbing
JAMA Neurol 77:129-130, Paliwal, V.K.,et al, 2020
Contrast-Induced Encephalopathy Following Coronary Angiography
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Clinicopathologic Conference, Borrelia Miyamotoi Infection
NEJM 383:1578-1586, Case 32-2020, 2020
An 11-year-old girl with focal seizures, fevers, and unilateral, enhancing cortical lesions
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A 14-Year-Old Girl with Headache, Seizures, and Confusion
Neurol 92:e161-e167, Xiao, L.,et al, 2019
Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 2019
Seizures and Encephalitis in Myelin Oligodendrocyte Glycoprotein IgG Disease vs Aquaporin 4 IgG Disease
JAMA Neurol 75:65-71, Hamid, S.H.M.,et al, 2018
Clinicopathologic Conference, Homocystinuria due to genetic mutations of the gene encoding cystathionine B-synthase (CBS)
NEJM 378:941-948, Case 7-2018, 2018
An 18-year-old man with progressive headache and visual loss
Neurol 90:1076-1081, Jiang, N.,et al, 2018
Pantothenate Kinase - Associated Neurodegeneration (PKAN)
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Behcet Disease
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FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
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Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
JAMA Neurol 74:737-740, Cohen, A.L.,et al, 2017
A Patient with a History of Encephalomyelitis and Recurrent Optic Neuritis
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Distinguishing Neuroimaging Features in Patients Presenting with Visual Hallucinations
AJNR 37:774-781, Winton-Brown, T.T.,et al, 2016
Resective Epilepsy Surgery for Drug-Resistant Focal Epilepsy
JAMA 313:285-293, Jobst, B.C. & Cascino, G.D., 2015
Acute-Onset Homonymous Hemianopia with Hyperglycemia
Neurol 82:e129-e133, Strowd, R.E.,et al, 2014
Epileptic Kinetopsia Localizes to Superior Parietal Lobule and Intraparietal Sulcus
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Sturge-Weber Syndrome
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The Acquired Metabolic Disorders of the Nervous System, Carbon Monoxide Poisoning
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Alcohol and Alcoholism
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Inherited Metabolic Diseases of the Nervous System, Tay Sachs Disease
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Inherited Metabolic Diseases of the Nervous System, Infantile Niemann-Pick Disease
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Brain Abnormalities as an Initial Manifestation of Neuromyelitis Optica Spectrum Disorder
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Subacute Sclerosing Panencephalitis
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Variable Presentations of Postpartum Angiopathy
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Central Nervous System Involvement in Dengue
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MELAS
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Presentation, Diagnosis, Pathophysiology, and Treatment of the Neurological Features of Sturge-Weber Syndrome
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Brain Biopsy in Children With Primary Small-Vessel Central Nervous System Vasculitis
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