Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency

Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defect

(2011) Y. G. Weber et al.   NEUROLOGY

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

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

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

Autosomal Recessive Inheritance of GLUT1 Deficiency Syndrome

(2010) J. Klepper et al.   NEUROPEDIATRICS

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

(2009) Arvid Suls et al.   ANNALS OF NEUROLOGY

GLUT1 DEFICIENCY AND ALTERNATING HEMIPLEGIA OF CHILDHOOD

(2009) M. Rotstein et al.   NEUROLOGY

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

(2008) A. Suls et al.   BRAIN

GLUT1 Deficiency Without Epilepsy: Yet Another Case

(2008) Charuta Joshi et al.   JOURNAL OF CHILD NEUROLOGY

Glut1 deficiency: CSF glucose. How low is too low?

(2008) D.C. De Vivo et al.   REVUE NEUROLOGIQUE