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

Model of the Exofacial Substrate-Binding Site and Helical Folding of the Human Glut1 Glucose Transporter Based on Scanning Mutagenesis

(2009) Mike Mueckler et al.   BIOCHEMISTRY

The expanding phenotype of GLUT1-deficiency syndrome

(2009) Knut Brockmann   BRAIN & DEVELOPMENT

New GLUT-1 mutation in a child with treatment-resistant epilepsy

(2009) Laurel Slaughter et al.   EPILEPSY RESEARCH

GLUT1 gene mutations cause sporadic paroxysmal exercise-induced dyskinesias

(2009) Susanne A. Schneider et al.   MOVEMENT DISORDERS

Le syndrome de déficit en GLUT-1 ou maladie de De Vivo : à propos d’un cas

(2008) I. Ticus et al.   ARCHIVES DE PEDIATRIE

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

(2008) A. Suls et al.   BRAIN

Glut-1 deficiency syndrome masquerading
 as idiopathic generalized epilepsy

(2008) Eliane Roulet-Perez et al.   EPILEPSIA

Molecular analysis and anticonvulsant therapy in two patients with glucose transporter 1 deficiency syndrome: A successful use of zonisamide for controlling the seizures

(2008) Satoru Takahashi et al.   EPILEPSY RESEARCH

GLUT1 Deficiency Without Epilepsy: Yet Another Case

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

Paroxysmal movement disorders in GLUT1 deficiency syndrome

(2008) G. Zorzi et al.   NEUROLOGY

Modified Atkins diet therapy for a case with glucose transporter type 1 deficiency syndrome

(2007) Susumu Ito et al.   BRAIN & DEVELOPMENT