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Brain & Development|September 19, 2015
A mild case of giant axonal neuropathy without central nervous system manifestationReiko Koichihara, Takashi Saito, Akihiko Ishiyama, et al.Brain & Development|October 21, 2015
High prevalence of genetic alterations in early-onset epileptic encephalopathies associated with infantile movement disordersYu Kobayashi, Jun Tohyama, Mitsuhiro Kato, et al.Brain & Development|December 10, 2014
Nationwide survey of glucose transporter-1 deficiency syndrome (GLUT-1DS) in JapanYasushi Ito, Satoru Takahashi, Kuriko Kagitani-Shimono, et al.Brain & Development|December 11, 2014
Identification and functional study of novel PLP1 mutations in Chinese patients with Pelizaeus-Merzbacher diseaseHan Xie, Hongchun Feng, Jinhua Ji, et al.Brain & Development|October 31, 2015
MRI and MRS findings in fucosidosis; a rare lysosomal storage diseaseSuna Sahin Ediz, Ayse Aralasmak, Temel Fatih Yilmaz, et al.Brain & Development|November 19, 2015
Bilateral ophthalmoplegia in a child with migraineRachana Dubey, Biswaroop Chakrabarty, Lokesh Saini, et al.Brain & Development|March 1, 2016
A novel PIGA mutation in a family with X-linked, early-onset epileptic encephalopathyYoung Ok Kim, Jae Hyuk Yang, Chungoo Park, et al.Brain & Development|February 13, 2016
Focal seizures and epileptic spasms in a child with Down syndrome from a family with a PRRT2 mutationAyuko Igarashi, Akihisa Okumura, Keiko Shimojima, et al.Brain & Development|March 17, 2016
Refractory and severe status epilepticus in a patient with ring chromosome 20 syndromeYoshiko Hirano, Hirokazu Oguni, Satoru NagataBrain & Development|April 14, 2016
Trends in the prevalence of cerebral palsy in children born between 1988 and 2007 in Okinawa, JapanMayumi Touyama, Jun Touyama, Satoshi Toyokawa, et al.Pageof 483