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Brain & Development|July 9, 2017
A patient with early myoclonic encephalopathy (EME) with a de novo KCNQ2 mutationKarin Kojima, Kentaro Shirai, Mizuki Kobayashi, et al.Brain & Development|May 8, 2018
Treatment of infantile spasms by pediatric neurologists in JapanShin-Ichiro Hamano, Toshisaburo Nagai, Ryuki Matsuura, et al.Brain & Development|April 12, 2018
Long-term home non-invasive positive pressure ventilation in children: Results from a single center in JapanAzusa Ikeda, Megumi Tsuji, Tomohide Goto, et al.Brain & Development|January 1, 1987
Muscle involvement in pyruvate dehydrogenase complex (PDHC) deficiencyS J Chung, S Asoh, T Yamanaka, et al.Brain & Development|May 11, 2019
Prediction of poor neurological development in patients with symptomatic congenital cytomegalovirus diseases after oral valganciclovir treatmentSachiyo Fukushima, Ichiro Morioka, Shohei Ohyama, et al.Brain & Development|April 29, 2019
Rapid progression of a walking disability in a 5-year-old boy with a CLN6 mutationAyumi Matsumoto, Masako Nagashima, Kazuhiro Iwama, et al.Brain & Development|September 30, 2017
Correlations between UGT2B7∗2 gene polymorphisms and plasma concentrations of carbamazepine and valproic acid in epilepsy patientsHui Zhang, Wenfang Zhang, Yuechun Li, et al.Brain & Development|January 1, 1988
The moment of intraventricular hemorrhageM Funato, H Tamai, R Kodaka, et al.Brain & Development|March 26, 2018
A case of severe Alexander disease with de novo c. 239 T > C, p.(F80S), in GFAPAyumi Matsumoto, Janyerkye Tulyeu, Rieko Furukawa, et al.Pageof 479