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Metabolic Lipid Muscle Disorders: Biomarkers and Treatment
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Clinicopathologic Conference, Posterior Cortical Atrophy with Frontotemporal Lobe Dementia with Gene Mutation
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Absence Epilepsies With Widely Variable Onset are a Key Feature of Familial GLUT1 Deficiency
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The Expanding Phenotype of GLUT1-Deficiency Syndrome
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