
Clinical Variability of GLUT1DS
References
- De Giorgis V Teutonico F Cereda C Balottin U Bianchi M Giordano L Sporadic and familial glut1ds Italian patients: A wide clinical variability Seizure 2015 Jan 24 28 32 10.1016/j.seizure.2014.11.009 25564316
- Brockmann K The expanding phenotype of GLUT1-deficiency syndrome Brain Dev. 2009 31 7 545 52 10.1016/j.braindev.2009.02.008 19304421
- Byrne S Kearns J Carolan R Mc Menamin J Klepper J Webb D Refractory absence epilepsy associated with GLUT-1 deficiency syndrome Epilepsia 2011 52 5 1021 4 10.1111/j.1528-1167.2011.02989.x 21366555
- Brockmann K Wang D Korenke CG von Moers A Ho YY Pascual JM Autosomal dominant glut-1 deficiency syndrome and familial epilepsy Ann Neurol. 2001 50 4 476 85 11603379
- Leen WG Klepper J Verbeek MM Leferink M Hofste T van Engelen BG Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder Brain 2010 133 Pt 3 655 70 10.1093/brain/awp336 20129935
- Wang D Pascual JM Yang H Engelstad K Jhung S Sun RP Glut-1 deficiency syndrome: clinical, genetic, and therapeutic aspects Ann Neurol. 2005 57 1 111 8 10.1002/ana.20331 15622525
- Klepper J Absence of SLC2A1 mutations does not exclude Glut1 deficiency syndrome Neuropediatrics 2013 44 4 235 6 10.1055/s-0033-1336015 23483445
DOI: https://doi.org/10.15844/pedneurbriefs-29-2-5 | Journal eISSN: 2166-6482
Language: English
Page range: 14 - 14
Submitted on: Feb 5, 2015
Accepted on: Feb 10, 2015
Published on: Feb 25, 2015
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
Keywords:
© 2015 Anastasia Martinez-Esteve Melnikova, Christian M Korff, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.