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Brain & Development|August 3, 2012
Acute severe encephalopathy related to human herpesvirus-6 infection in a patient with carnitine palmitoyltransferase 2 deficiency carrying thermolabile variantsYoshiyuki Kobayashi, Nobutsune Ishikawa, Miyuki Tsumura, et al.Brain & Development|August 15, 2012
A long-term, clinical study on symptomatic infantile spasms with focal featuresAkiko Fujii, Hirokazu Oguni, Yoshiko Hirano, et al.Brain & Development|January 1, 1990
Visual and auditory evoked potential correlates of cerebral malformationsS G Coupland, H B SarnatBrain & Development|January 1, 1990
Electron microscopic study on the homozygote (Ml/Ml) of the macular mutant mouseS Iwane, T Yamano, M ShimadaBrain & Development|January 1, 1990
Muscle involvement in mucolipidosis IVR Weitz, I Kramer, I Nissenkorn, et al.Brain & Development|January 1, 1990
Crossed cerebellar diaschisis in the Sturge-Weber syndromeH Yoshikawa, N Fueki, N Sakuragawa, et al.Brain & Development|June 28, 2020
Glucose transporter type 1 deficiency syndrome associated with autoantibodies to glutamate receptorsHiroki Hoshino, Kazuko Takayama, Atsushi Ishii, et al.Brain & Development|June 30, 2020
A recurrent TMEM106B mutation in hypomyelinating leukodystrophy: A rapid diagnostic assaySatoru Ikemoto, Shin-Ichiro Hamano, Kenjiro Kikuchi, et al.Brain & Development|July 1, 2020
Single gene, two diseases, and multiple clinical presentations: Biotin-thiamine-responsive basal ganglia diseaseBetül Kılıç, Yasemin Topçu, Şiar Dursun, et al.Brain & Development|October 20, 2012
14-3-3 proteins, particularly of the epsilon isoform, are detectable in cerebrospinal fluids of cerebellar diseases in childrenKatsunori Fujii, Hideki Uchikawa, Yuzo Tanabe, et al.Pageof 482