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Journal of pediatric neurosciences, ISSN 1817-1745, 10/2018, Volume 13, Issue 4, pp. 496 - 499
Glucose transporter type 1 deficiency syndrome (GLUT1-DS) was first described by De Vivo in 1991, and the classic clinical manifestations include infantile... 
Ataxia | Genetic aspects | Research | Gene mutations | Pediatric research | Biological transport | Genes | Epilepsy | Physiological aspects | Glucose | Dextrose | Genotype & phenotype | Convulsions & seizures | Gait | Biomarkers | Electroencephalography | Mutation | Microcephaly | Patients | SLC2A1 gene | movement disorder | ketogenic diet | Glucose transporter type 1 deficiency syndrome | Case Report
Journal Article
Neuropediatrics, ISSN 0174-304X, 04/2018, Volume 49, Issue S 01, pp. S1 - S12
Conference Proceeding
Developmental Medicine & Child Neurology, ISSN 0012-1622, 09/2019, Volume 61, Issue 9, pp. 1101 - 1107
Relapses of anti‐N‐methyl‐D‐aspartate receptor encephalitis may span over a long period. Relapses were not associated with severity in the acute phase or... 
ANTIBODIES | AUTOIMMUNE | CSF | PEDIATRICS | CEREBROSPINAL-FLUID | CLINICAL NEUROLOGY | CHILDREN
Journal Article
Journal Article
PLoS Genetics, ISSN 1553-7390, 05/2015, Volume 11, Issue 5, p. e1005232
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2014, Volume 9, Issue 10, p. e108205
Journal Article
PLoS ONE, ISSN 1932-6203, 01/2013, Volume 8, Issue 1, p. e52512
Journal Article
BMC Medical Genetics, ISSN 1471-2350, 08/2012, Volume 13, Issue 1, pp. 73 - 73
Journal Article
BMC Genomics, ISSN 1471-2164, 05/2011, Volume 12, Issue 1, pp. 235 - 235
Journal Article
PLoS ONE, ISSN 1932-6203, 01/2014, Volume 9, Issue 1, p. e83400
Journal Article
14.