Glucose transporter 1 deficiency in the idiopathic generalized epilepsies

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

(2011) Saul A. Mullen   ARCHIVES OF NEUROLOGY

Stomatin-deficient cryohydrocytosis results from mutations in SLC2A1: a novel form of GLUT1 deficiency syndrome

(2011) J. F. Flatt et al.   BLOOD

Familial clustering of epilepsy and behavioral disorders: Evidence for a shared genetic basis

(2011) Dale C. Hesdorffer et al.   EPILEPSIA

Glut1 deficiency: Inheritance pattern determined by haploinsufficiency

(2010) Michael Rotstein et al.   ANNALS OF NEUROLOGY

Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder

(2010) W. G. Leen et al.   BRAIN

Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005-2009

(2010) Anne T. Berg et al.   EPILEPSIA

Frequency of Epilepsies in Family Members of Patients with Different Epileptic Syndromes

(2010) Vedat Sozmen et al.   EUROPEAN NEUROLOGY

Astroglial networks: a step further in neuroglial and gliovascular interactions

(2010) Christian Giaume et al.   NATURE REVIEWS NEUROSCIENCE

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

(2010) S. A. Mullen et al.   NEUROLOGY

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

(2009) Arvid Suls et al.   ANNALS OF NEUROLOGY

Augmented currents of an HCN2 variant in patients with febrile seizure syndromes

(2009) Leanne M. Dibbens et al.   ANNALS OF NEUROLOGY

Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1

(2008) A. Suls et al.   BRAIN

Navigating the channels and beyond: unravelling the genetics of the epilepsies

(2008) Ingo Helbig et al.   LANCET NEUROLOGY

Functional Studies of the T295M Mutation Causing Glut1 Deficiency: Glucose Efflux Preferentially Affected by T295M

(2008) Dong Wang et al.   PEDIATRIC RESEARCH