The role ofSLC2A1mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome

The incidence ofSCN1A-related Dravet syndrome in Denmark is 1:22,000: A population-based study from 2004 to 2009

(2015) Allan Bayat et al.   EPILEPSIA

Long-Term Clinical Course of Glut1 Deficiency Syndrome

(2014) Aliza S. Alter et al.   JOURNAL OF CHILD NEUROLOGY

Phenotypic Spectrum of Glucose Transporter Type 1 Deficiency Syndrome (Glut1 DS)

(2013) Toni S. Pearson et al.   Current Neurology and Neuroscience Reports

The role of SLC2A1 in early onset and childhood absence epilepsies

(2013) Hiltrud Muhle et al.   EPILEPSY RESEARCH

Glucose transporter 1 deficiency in the idiopathic generalized epilepsies

(2012) Todor Arsov et al.   ANNALS OF NEUROLOGY

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

(2011) Saul A. Mullen   ARCHIVES OF NEUROLOGY

Absence seizures with intellectual disability as a phenotype of the 15q13.3 microdeletion syndrome

(2011) Hiltrud Muhle et al.   EPILEPSIA

Video/EEG recording of myoclonic absences in GLUT1 deficiency syndrome with a hot-spot R126C mutation in the SLC2A1 gene

(2011) Sarenur Gökben et al.   EPILEPSY & BEHAVIOR

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

(2010) W. G. Leen et al.   BRAIN

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

(2009) Arvid Suls et al.   ANNALS OF NEUROLOGY

15q13.3 microdeletions increase risk of idiopathic generalized epilepsy

(2009) Ingo Helbig et al.   NATURE GENETICS