The Many Faces of Glut1 Deficiency Syndrome

Glucose transporter type I deficiency syndrome: Epilepsy phenotypes and outcomes

(2012) Amanda W. Pong et al.   EPILEPSIA

Glut1 deficiency syndrome and erythrocyte glucose uptake assay

(2011) Hong Yang et al.   ANNALS OF NEUROLOGY

Glucose transporter type 1 deficiency syndrome with carbohydrate-responsive symptoms but without epilepsy

(2011) ANNE KOY et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

A modified Atkins diet is promising as a treatment for glucose transporter type 1 deficiency syndrome

(2011) YASUSHI ITO et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Glut1 deficiency: When to suspect and how to diagnose?

(2011) A. Verrotti et al.   EUROPEAN JOURNAL OF PAEDIATRIC 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

Excellent response to acetazolamide in a case of paroxysmal dyskinesias due to GLUT1-deficiency

(2010) Mathieu Anheim et al.   JOURNAL OF NEUROLOGY

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

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

The expanding phenotype of GLUT1-deficiency syndrome

(2009) Knut Brockmann   BRAIN & DEVELOPMENT

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