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Brain & Development|July 22, 2014
A novel PLP1 frameshift mutation causing a milder form of Pelizaeus-Merzbacher diseaseTakashi Shiihara, Mio Watanabe, Kengo Moriyama, et al.Brain & Development|July 22, 2014
EEG activation by neuropsychological tasks in idiopathic generalized epilepsy of adolescenceGiedrė Gelžinienė, Milda Endzinienė, Giedrė JurkevičienėBrain & Development|July 24, 2014
Effect of early intervention on premature infants' general movementsLiang Ma, Bingshang Yang, Lingdan Meng, et al.Brain & Development|January 1, 1986
Auditory brain stem responses(ABR) in developmentally retarded infants and childrenY Mochizuki, H Ohkubo, A Yoshida, et al.Brain & Development|November 5, 2013
Novel SETX variants in a patient with ataxia, neuropathy, and oculomotor apraxia are associated with normal sensitivity to oxidative DNA damaging agentsChiara Vantaggiato, Orazio Cantoni, Andrea Guidarelli, et al.Brain & Development|August 28, 2013
Differences between periventricular hemorrhagic infarction and periventricular leukomalaciaTakeshi Tsuji, Akihisa Okumura, Hiroyuki Kidokoro, et al.Brain & Development|August 21, 2013
Metabolic encephalopathy in beta-ketothiolase deficiency: the first report from IndiaRadha Rama Devi Akella, Yuka Aoyama, Chihiro Mori, et al.Brain & Development|August 24, 2013
Carnitine palmitoyltransferase 2 gene polymorphism is a genetic risk factor for sudden unexpected death in infancyTakuma Yamamoto, Hidekazu Tanaka, Yuko Emoto, et al.Brain & Development|January 1, 1990
Prognosis for seizure control in infantile spasms preceded by other seizuresA Velez, O Dulac, P PlouinBrain & Development|January 1, 1990
Sexual dimorphism of the human corpus callosum studied by magnetic resonance imaging: fact, fallacy and statistical confidenceA D Elster, D A DiPersio, D M MoodyPageof 482