A Proposed Diagnostic Scheme for People with Epileptic Seizures and with Epilepsy: Report of the ILAE Task Force on Classification and Terminology

Jerome Engel

Epilepsia

Defective Glucose Transport across the Blood-Brain Barrier as a Cause of Persistent Hypoglycorrhachia, Seizures, and Developmental Delay

Darryl C. De Vivo, Rosario Rich Trifiletti, Ronald I. Jacobson, +3

New England Journal of Medicine

Lipid MovementCellular PhysiologyCerebral Vascular RegulationEssential FuelMembrane Transport +21

Maturational Changes in Cerebral Function in Infants Determined by ¹⁸ FDG Positron Emission Tomography

Harry T. Chugani, Michael E. Phelps

Science

Glut‐1 deficiency syndrome: Clinical, genetic, and therapeutic aspects

Dong Wang, Juan M. Pascual, Hong Yang, +4

Annals of Neurology

Neurological DisorderImmunodeficienciesImmunologyPathologySocial Sciences +21

Early‐onset absence epilepsy caused by mutations in the glucose transporter GLUT1

Arvid Suls, Saul A. Mullen, Yvonne Weber, +12

Annals of Neurology

Absence EpilepsiesEarly-onset Absence EpilepsyEarly‐onset Absence EpilepsyGeneticsGenetic Epidemiology +15

The spectrum of movement disorders in Glut‐1 deficiency

Roser Pons, Abbie Collins, Michael Rotstein, +2

Movement Disorders

Autosomal dominant Glut‐1 deficiency syndrome and familial epilepsy

Knut Brockmann, Dong Wang, Christoph Korenke, +10

Annals of Neurology

Absence epilepsies with widely variable onset are a key feature of familial GLUT1 deficiency

Saul A. Mullen, Arvid Suls, Peter De Jonghe, +2

Neurology

Seizure Control and Acceptance of the Ketogenic Diet in GLUT1 Deficiency Syndrome: A 2- to 5-Year Follow-Up of 15 Children Enrolled Prospectively

Jörg Klepper, Hans Scheffer, B. Leiendecker, +7

Neuropediatrics

Glucose Transporter 1 Deficiency as a Treatable Cause of Myoclonic Astatic Epilepsy

Saul A. Mullen, Carla Marini, Arvid Suls, +10

Archives of Neurology