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Brain & Development|November 3, 2018
Reversible splenial lesion syndrome in children with benign convulsions associated with mild gastroenteritis: A retrospective study of five casesLihua Jiang, Shanshan Mao, Jialu Xu, et al.Brain & Development|November 3, 2018
A case of dihydropyrimidinase deficiency incidentally detected by urine metabolome analysisHiroki Tsuchiya, Tomoyuki Akiyama, Tomiko Kuhara, et al.Brain & Development|November 6, 2018
A case of early onset life-threatening epilepsy associated with a novel ATP1A3 gene variantNaoko Ishihara, Hidehito Inagaki, Misa Miyake, et al.Brain & Development|November 17, 2016
A ten-year follow-up cohort study of childhood epilepsy: Changes in epilepsy diagnosis with ageYoshiyuki Hanaoka, Harumi Yoshinaga, Katsuhiro KobayashiBrain & Development|November 16, 2016
Hyperekplexia: Report on phenotype and genotype of 16 Jordanian patientsAmira Masri, Seo-Kyung Chung, Mark I ReesBrain & Development|October 5, 2016
Neurodevelopmental outcome of term infants with perinatal asphyxia with hypoxic ischemic encephalopathy stage IISudhir Adhikari, Kalipatnam Seshagiri RaoBrain & Development|October 5, 2016
Early cardiac involvement in an infantile Sandhoff disease case with novel mutationsHsiu-Fen Lee, Ching-Shiang Chi, Chi-Ren TsaiBrain & Development|October 30, 2016
A novel PLP1 mutation associated with optic nerve enlargement in two siblings with Pelizaeus-Merzbacher disease: A new MRI findingEfterpi Pavlidou, Vijaya Ramachandran, Veronica Govender, et al.Brain & Development|December 8, 2016
Total corpus callosotomy for epileptic spasms after acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) in a case with tuberous sclerosis complexTohru Okanishi, Ayataka Fujimoto, Hirotaka Motoi, et al.Brain & Development|December 9, 2016
Novel mutation in a patient with late onset GLUT1 deficiency syndromeSandra Juozapaite, Ruta Praninskiene, Birute Burnyte, et al.Pageof 482