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Brain & Development|December 31, 2014
Early onset of moyamoya syndrome in a Down syndrome patient with the genetic variant RNF213 p.R4810KPin Fee Chong, Reina Ogata, Hatasu Kobayashi, et al.Brain & Development|December 7, 2014
Rub epilepsy in an infant with Turner syndromeShin-Ichi Magara, Hideshi Kawashima, Yu Kobayashi, et al.Brain & Development|December 7, 2014
Development of a practical NF1 genetic testing method through the pilot analysis of five Japanese families with neurofibromatosis type 1Akiko Okumura, Mamoru Ozaki, Yo NiidaBrain & Development|December 4, 2014
Myocerebrohepatopathy spectrum disorder due to POLG mutations: A clinicopathological reportHesham Montassir, Yoshihiro Maegaki, Kei Murayama, et al.Brain & Development|January 16, 2020
The correlation between the evolution of bilateral basal ganglia hemorrhage using MR imaging and neurological damage recovery in an infant with methylmalonic aciduriaBin Guo, Linfeng Yang, Xue Li, et al.Brain & Development|September 11, 2020
Early prediction of encephalopathic transformation in children with benign epilepsy with centro-temporal spikesAdi Porat Rein, Uri Kramer, Moran Hausman Kedem, et al.Brain & Development|September 3, 2020
Postoperative improvement of executive function and adaptive behavior in children with intractable epilepsyRiyo Ueda, Yoshimi Kaga, Yosuke Kita, et al.Brain & Development|September 5, 2020
Initial treatment of seizures in children in an emergency department in rural JapanAnna Shiraki, Masahiro Yasui, Hiroyuki Kidokoro, et al.Brain & Development|September 7, 2020
Clinical utility of the FilmArray meningitis/encephalitis panel in children at a tertiary center in South KoreaSu Eun Park, Taek Jin Lim, Sang Ook Nam, et al.Brain & Development|November 24, 2020
Polymicrogyria with calcification in Pallister-Killian syndrome detected by microarray analysisAkiko Hiraiwa, Kou Matsui, Yumi Nakayama, et al.Pageof 482