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Hypointensity of the Basal Ganglia in Adults with Glucose Transporter Protein Type 1 Deficiency Syndrome: A Novel Magnetic Resonance Imaging Finding
Ann Neurol 87:10-11, Van Samkar, A.,et al, 2020
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Clinicopathologic Conference, Creutzfeldt-Jakob Disease
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Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
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A Syndrome of Bilateral Symmetrical Basal Ganglia Lesions in Diabetic Dialysis Patients
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Fulminant Encephalopathy With Basal Ganglia Hyperintensities in HIV-Infected Drug Users
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