Mild adolescent/adult onset epilepsy and paroxysmal exercise-induced dyskinesia due to GLUT1 deficiency
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1167.2010.02726.x/fullpdf
Reference10 articles.
1. Autosomal dominant GLUT1 deficiency syndrome and familial epilepsy;Brockmann;Ann Neurol,2001
2. Defective glucose transport across the blood-brain barrier as a cause of persistent hypoglycorrhachia, seizures, and developmental delay;De Vivo;N Engl J Med,1991
3. Autosomal dominant transmission of GLUT1 deficiency;Klepper;Hum Mol Genet,2001
4. GLUT1 deficiency syndrome-2007 update;Klepper;Dev Med Child Neurol,2007
5. Familial paroxysmal excercise-induced dyskinesia and benign epilepsy: a clinical and neurophysiological study of an uncommon disorder;Margari;Neurol Sci,2000
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3. The role of molecular analysis of SLC2A1 in the diagnostic workup of glucose transporter 1 deficiency syndrome;Journal of the Neurological Sciences;2020-09
4. Glucose transporter type I deficiency and other glucose flux disorders;Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease;2020
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