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Brain & Development|November 3, 2010
Serial MRI changes in a patient with infantile Alexander disease and prolonged survivalTakashi Shiihara, Toru Yoneda, Ikuko Mizuta, et al.Brain & Development|November 30, 2010
Pathology, clinical features and treatments of congenital copper metabolic disorders--focus on neurologic aspectsHiroko Kodama, Chie Fujisawa, Wattanaporn BhadhprasitBrain & Development|January 1, 1990
Molecular analysis of the Rett syndrome using cDNA synapsin I as a probeA Ferlini, L Ansaloni, C Nobile, et al.Brain & Development|October 19, 2010
Restless Leg Syndrome in ADHD children: levetiracetam as a reasonable therapeutic optionAntonella Gagliano, Irene Aricò, Tiziana Calarese, et al.Brain & Development|November 16, 2010
Rud syndrome with focal cortical dysplasia: a case reportSara Marconi, Gaetano Cantalupo, Federica Marliani, et al.Brain & Development|March 16, 2013
Clinical analysis of catastrophic epilepsy in infancy and early childhood: results of the Far-East Asia Catastrophic Epilepsy (FACE) study groupHirokazu Oguni, Taisuke Otsuki, Katsuhiro Kobayashi, et al.Brain & Development|February 7, 2013
Magnetoencephalography localizing spike sources of atypical benign partial epilepsyHideaki Shiraishi, Kazuhiro Haginoya, Eiji Nakagawa, et al.Brain & Development|March 5, 2013
Effect of a blackout in pediatric patients with home medical devices during the 2011 eastern Japan earthquakeTojo Nakayama, Soichiro Tanaka, Mitsugu Uematsu, et al.Brain & Development|April 16, 2013
MELAS phenotype associated with m.3302A>G mutation in mitochondrial tRNA(Leu(UUR)) geneMasahide Goto, Hirofumi Komaki, Takashi Saito, et al.Brain & Development|April 17, 2013
Impaired function of the auditory brainstem in term neonates with hyperbilirubinemiaZe D Jiang, Andrew R WilkinsonPageof 483