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Brain & Development|June 11, 2015
Pediatric epilepsy following neonatal seizures symptomatic of strokeAgnese Suppiej, Massimo Mastrangelo, Laura Mastella, et al.Brain & Development|August 16, 2016
A case of Dravet syndrome with cortical myoclonus indicated by jerk-locked back-averaging of electroencephalogram dataYoshinori Kobayashi, Yoshiyuki Hanaoka, Tomoyuki Akiayma, et al.Brain & Development|January 1, 1981
Febrile convulsions and rolandic dischargesT Kajitani, K Ueoka, M Nakamura, et al.Brain & Development|March 17, 2018
Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life spanDidem Yücel-Yılmaz, Emrah Yücesan, Dilek Yalnızoğlu, et al.Brain & Development|March 20, 2018
Ambulatory capacity in Japanese patients with Duchenne muscular dystrophyHiroyuki Awano, Chieko Itoh, Yasuhiro Takeshima, et al.Brain & Development|January 9, 2018
Scalp-recorded high-frequency oscillations in childhood epileptic encephalopathy with continuous spike-and-wave during sleep with different etiologiesPan Gong, Jiao Xue, Ping Qian, et al.Brain & Development|January 27, 2018
Quantitative microstructural cerebral changes in neurofibromatosis type 1Eva Bültmann, Loukia M Spineli, Hans Hartmann, et al.Brain & Development|March 31, 2018
Anti-N-methyl-d-aspartate receptor encephalitis in children: Incidence and experience in Hong KongAlvin Chi-Chung Ho, Sophelia Hoi-Shan Chan, Eric Chan, et al.Brain & Development|March 5, 2018
Fazio-Londe syndrome in siblings from India with different phenotypesVykuntaraju K Gowda, Tamilarasan Udhayabanu, Perumal Varalakshmi, et al.Brain & Development|March 6, 2018
A novel germline PIGA mutation causes early-onset epileptic encephalopathies in Chinese monozygotic twinsLing-Ling Xie, Xiao-Jie Song, Tian-Yi Li, et al.Pageof 483