Expanding Clinical Spectrum an Anti-GQ1b Antibody Syndrome, A Review
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Cranial Pachymeningitis of Unknown Origin:A Study of Seven Cases
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Neurological Problems in Endocrine Diseases
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Neurologic Manifestations of SLE 1972
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A 16-Year-Old Adolescent Boy with Ophthalmoplegia and Unilateral Ptosis
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Clinicopathologic Conference, Myeloperoxidase antineutrophil cytoplasmic antibody-associated vasculitis
NEJM 390:843-851, Case 7-2024, 2024
Intracranial Hypertension Associated with Poly-Cranio-Radicular-Neuropathies A Case Report and Review of the Literature
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Cavernous Sinus Thrombosis
StatPearls PMID:28846357, Plewa,M.C.,et al, 2023
An 82-Year-Old Woman with Subacute Ophthalmoparesis and Ataxia
Neurol 101:e570-e575, Rodrigo-Gisbert,M.,et al, 2023
Idiopathic Orbital Inflammation and Tolosa-Hunt Syndrome with Intracranial Extension
Neurol 101:371-374, Yu,S. & Chen,T., 2023
A 67-Year-Old Woman with Progressive Diplopia, Vertigo, and Ataxia
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Miller Fisher Syndrome and Acute Motor and Sensory Axonal Neuropathy (AMSAN) Variant Guillain-Barre Overlap Syndrome (MFS/AMSAN-GBS) After Upper Respiratory Tract Infection (URTI)
Acta Sci Clin Case Reports 3:19-24, Chau,T.C. & Muhamad,N.A.N., 2022
Nonalcoholic Wernicke Encephalopathy
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Relapsing-Remitting Severe Bickerstaffs Brainstem Encephalitis
BMJ 394:684, Tyrakowska, Z.,et al, 2019
Bilateral Claude Syndrome
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Rare Presentation of Spontaneous, Direct, Carotid Cavernous Fistula in Late Pregnancy:A Case Report
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Proptosis and Double Vision in a Child
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A 35-year-old Woman with Diplopia, Ataxia, and Altered Mental Status
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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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
Acute Bulbar Palsy as a Variant of Guillain-Barre Syndrome
Neurol 86:742-747, Kim, J.K.,et al, 2016
A 20-year-old Man with Headache and Double Vision
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Diseases of the Nervous System Caused by Nutritional Deficiency, Wernicke-Korsakoff Syndrome (Thiamine B1) Deficiency
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Diseases of the Nervous System Caused by Nutritional Deficiency, Vitamin E Deficiency
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Disturbances of Cerebrospinal Fluid, Including Hydrocephalus, Pseudotumor Cerebri, and Low-Pressure Syndromes, Increased Intracranial Pressure
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Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Legionella
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Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Whipple Disease
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Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Septic Cavernous Sinus Thrombophlibitis
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Ptosis, Erythema, and Rapidly Decreasing Vision
JAMA 309:2382-2383, Zanation, A.,et al, 2013
Central Nervous System Involvement in Whipple Disease
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Bilirubin-Induced Neurologic Damage - Mechanisms and Management Approaches
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Miller Fisher Syndrome with Positivity of Anti-GAD Antibodies
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Clinicopathologic Conference, Squamous- Cell Carcinoma of the Tongue with Metastasis to Lungs, Liver, Bone of Skull, Trigeminal Nerve, Base of Skull, Pituitary Gland and Dura Matter. Infarcts of Cerebellum and Right Frontal Lobe.
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Rhino-orbitocerebral Mucormycosis Associated with Cavernous Sinus Thrombosis: Case Report
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Orbital Syndromes
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Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
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Mitochondrial DNA Polymerase-y and Human Disease
Hum Mol Genet 15:R244-R252, Hudson, G.,et al, 2006
Isolated Abducens Nerve Palsy as a Regional Variant of Guillain-Barre Syndrome
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Visual Loss Due to a Carious Tooth
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Mitochondrial Respiratory-Chain Diseases
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Vasogenic Edema in Bickerstaff's Brainstem Encephalitis
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Bickerstaff's Brainstem Encephalitis: Clinical Features of 62 Cases and a Subgroup Associated with Guillain-Barre Syndrome
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Dysthyroid Orbitopathy
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Neuro-Ophthalmic Manifestations of Diabetes
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Usefulness of CT and MR Imaging in the Diagnosis of Acute Wernickes Encephalopathy
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Neuro-Ophthalmic Manifestations of Lyme Disease
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Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
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