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Brain & Development|August 8, 2015
Fetal hydrocephalus and neonatal stroke as the first presentation of protein C deficiencyMasako Ichiyama, Shouichi Ohga, Masayuki Ochiai, et al.Brain & Development|October 8, 2015
Novel missense mutation in CLN8 in late infantile neuronal ceroid lipofuscinosis: The first report of a CLN8 mutation in JapanYu Katata, Mitsugu Uematsu, Hiroki Sato, et al.Brain & Development|October 12, 2015
Pre-school development and behavior screening with a consecutive support programs for 5-year-olds reduces the rate of school refusalSeigo Korematsu, Tomoyuki Takano, Tatsuro IzumiBrain & Development|July 22, 2017
Epileptic apnea in a patient with inherited glycosylphosphatidylinositol anchor deficiency and PIGT mutationsKosuke Kohashi, Akihiko Ishiyama, Shota Yuasa, et al.Brain & Development|July 22, 2017
KCNQ2 encephalopathy: A case due to a de novo deletionCarlotta Spagnoli, Grazia Gabriella Salerno, Alessandro Iodice, et al.Brain & Development|July 31, 2017
A novel mutation of WDR62 gene associated with severe phenotype including infantile spasm, microcephaly, and intellectual disabilityRosaria Nardello, Antonina Fontana, Vincenzo Antona, et al.Brain & Development|January 1, 1986
Behavioral and neurochemical changes in pups prenatally exposed to methamphetamineM Sato, Y FujiwaraBrain & Development|September 20, 2015
Loss-of-function mutations of STXBP1 in patients with epileptic encephalopathyToshiyuki Yamamoto, Keiko Shimojima, Tamami Yano, et al.Brain & Development|December 3, 2014
Infantile tauopathies: Hemimegalencephaly; tuberous sclerosis complex; focal cortical dysplasia 2; gangliogliomaHarvey B Sarnat, Laura Flores-SarnatBrain & Development|November 14, 2015
Clinical presentation, gene analysis and outcomes in young patients with early-treated combined methylmalonic acidemia and homocysteinemia (cblC type) in Shandong province, ChinaBingjuan Han, Zhiyang Cao, Liping Tian, et al.Pageof 483