A 23 years follow-up study identifies GLUT1 deficiency syndrome initially diagnosed as complicated hereditary spastic paraplegia
Author:
Funder
Canadian Institute for Health Research (CIHR)
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics,General Medicine
Reference18 articles.
1. Long-term clinical course of Glut1 deficiency syndrome;Alter;J. Child. Neurol.,2015
2. Autosomal dominant glut-1 deficiency syndrome and familial epilepsy;Brockmann;Ann. Neurol.,2001
3. Seizures, ataxia, developmental delay and the general paediatrician: glucose transporter 1 deficiency syndrome;Coman;J. Paediatr. Child. Health,2006
4. Sporadic and familial glut1ds Italian patients: a wide clinical variability;De Giorgis;Seizure,2015
5. 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
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