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The Tolosa-Hunt Syndrome
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Contrast-Induced Encephalopathy Following Coronary Angiography
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Pontine Warning Syndrome
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Giant Cell Arteritis With Unusual Flow-Related Neuroophthalmologic Manifestations
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Bilirubin Metabolism and Kernicterus
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Mitochondrial DNA and Disease
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Neurological Involvement in the Epidermal Naevus Syndrome
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Black Turbinate Sign as an Early Clue of Rhino-Orbital-Cerebral Mucormycosis
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Clinicopathologic Conference, Myeloperoxidase antineutrophil cytoplasmic antibody-associated vasculitis
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Progressive Cranial Neuropathy
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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)
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Relapsing-Remitting Severe Bickerstaffs Brainstem Encephalitis
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Rare Presentation of Spontaneous, Direct, Carotid Cavernous Fistula in Late Pregnancy:A Case Report
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A Child with Arthrogryposis
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Subacute Progressive Ptosis, Ophthalmoplegia, Gait Instability, and Cognitive Changes
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A Child with Delayed Motor Milestones and Ptosis
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Ptosis, Erythema, and Rapidly Decreasing Vision
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Central Nervous System Involvement in Whipple Disease
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Sarcoidosis: Clinical, Hormonal, and Magnetic Resonance Imaging (MRI) Manifestations of Hypothalamic-Pituitary Disease in 9 Patients and Review of the Literature
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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
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