Behcet Disease
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MELAS Presenting as Bilateral Symmetric Occipital and Temporal Cortices Lesions, A Case Report and Literature Review
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Focusing on the Eye Signs of Alport Syndrome in a 40-Year-Old Man Who Previously Had a Kidney Transplant and Hearing Loss
Lancet 401:e2, Kovalchuk,B. & Khoramnia,R., 2023
Neuroimaging Features of Biotinidase Deficiency
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A 31-Year-Old Man with Sequential Vision Loss
Neurol 98:163-169, Fortes, B.,et al, 2022
A 28-Year-Old Woman with Vision Loss and an Unusual Gait
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The Tolosa-Hunt Syndrome
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Homonymous Hemianopia with Normal Magnetic Resonance Imaging
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A 22-Year-Old Man with Progressive Bilateral Visual Loss
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A Woman with Monocular Vision Loss
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Clinicopathologic Conference, Borrelia Miyamotoi Infection
NEJM 383:1578-1586, Case 32-2020, 2020
Clinicopathologic Conference, Lebers Hereditary Optic Neuropathy
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Selenium Toxicity Associated with Reversible Leukoencephalopathy and Cortical Blindness
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A 10-year-old boy with Bilateral Vision Loss
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A Red Eye from Carotid Stenosis
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A Young Man with Progressive Vision and Hearing Loss
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Carotid-Cavernous Fistula
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Mystery Case: A 21-Year-Old Man with Visual Loss Following Marijuana Use
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Sudden Unilateral Painless Loss of Vision
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Giant-Cell Arteritis and Polymyalgia Rheumatica
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Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Septic Cavernous Sinus Thrombophlibitis
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Paraneoplastic Neurological Syndromes
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MELAS
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A 28-Year-Old Pregnant Woman with Encephalopathy
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A 23-Year-Old Man With Seizures and Visual Deficit
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Thrunderclap Headache--And a Tender Neck
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Neuro-Ophthalmic Manifestations of Sarcoidosis. Clincal Spectrum, Evaluation and Management
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Cerebroretinal Vasculopathy Mimicking a Brain Tumor:A Case of a Rare Hereditary Syndrome
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Retinocochleocerebral Vasculopathy
Medicine 77:12-40, Petty,G.W.,et al, 1998
Mucolipidosis Type IV; Characteristic MRI Findings
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Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
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Acquired Ocular Visual Impairment in Children, 1960-1989
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Leber's Hereditary Optic Neuropathy as a Cause of Severe Visual Loss in Childhood
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Atypical Leber's Hereditary Optic Neuropathy with Molecular Confiramtion
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Leber's Hereditary Optic Neuropathy, New Genetic Considerations
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The Management of Acute Visual Failure
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Progressive Vison Loss, A Rare Manifestation of Familial Cavernous Angiomas
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MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
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Hypertensive Encephalopathy:Findings on CT, MR Imaging, and SPECT Imaging in 14 Cases
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Neurologic Aspects of Cobalamin Deficiency
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Visual Loss in Tuberous Sclerosis
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A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy
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Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features
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Retinitis Pigmentosa
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Ocular Complications of Tangier Disease
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Sclerosteosis:Neurogenetic & Pathophysiologic Analysis of an American Kinship
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Gerstmann-Straussler-Scheinker Disease with Coincidental Familial Onset
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Two Cases of Van Buchem's Disease
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Leber's Optic Neuropathy
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