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Showing articles 0 to 8 of 8 Filter Applied: GLUT1 deficiency syndrome (Click to remove) 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 Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm JNNP 86:774-781, Van Egmond, M.E.,et al, 2015 Cerebrospinal Fluid Analysis in the Workup of GLUT1 Deficiency Syndrome JAMA Neurol 70:1440-1444, Leen, W.G.,et al, 2013 Differential Diagnosis of a Low CSF Glucose in Children and Young Adults Neurol 81:e178-e181, Leen, W.G.,et al, 2013 Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder Brain 133:655-670, Leen,W.G., et al, 2010 Absence Epilepsies With Widely Variable Onset are a Key Feature of Familial GLUT1 Deficiency Neurol 75:432-440, Mullen,S.A., et al, 2010 The Expanding Phenotype of GLUT1-Deficiency Syndrome Brain & Dev 31:545-552, Brockmann,K., 2009 Defective Glucose Transport Across the Blood-Brain Barrier as Cause of Hypoglycorrhachia, Seizures, and Devel Delay NEJM 325:703-709, 7311991., DeVivo,D.C.,et al, 1991 Showing articles 0 to 8 of 8