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Brain & Development|May 3, 2005
Modification of AMPA receptor properties following environmental enrichmentFumie Naka, Naoko Narita, Nobuo Okado, et al.Brain & Development|May 3, 2005
Clinical presentation, EEG studies, and novel mutations in two cases of GLUT1 deficiency syndrome in JapanYasushi Ito, Elena Gertsen, Hirokazu Oguni, et al.Brain & Development|August 27, 2005
Classic Rett syndrome in a boy with R133C mutation of MECP2Tatsuo Masuyama, Muneaki Matsuo, Jin J Jing, et al.Brain & Development|August 27, 2005
Prenatal stroke in a neonate heterozygous for factor V Leiden mutationAlfonso Verdu, María R Cazorla, Juan C Moreno, et al.Brain & Development|August 27, 2005
Longitudinal MR findings in a patient with hemimegalencephaly associated with tuberous sclerosisHiroshi Sakuma, Ohsuke Iwata, Masayuki SasakiBrain & Development|September 20, 2005
Mutational scanning of potassium, sodium and chloride ion channels in malignant migrating partial seizures in infancyGiangennaro Coppola, Pierangelo Veggiotti, Emanuele Miraglia Del Giudice, et al.Brain & Development|September 20, 2005
A case of massive gastric necrosis in a young girl with Rett SyndromeEmanuele Baldassarre, Giorgio Capuano, Gabriele Valenti, et al.Brain & Development|April 6, 2006
Adenoviral mediated MyoD gene transfer into fibroblasts: myogenic disease diagnosisIsao Fujii, Makoto Matsukura, Makoto Ikezawa, et al.Brain & Development|August 1, 2006
Hemiconvulsion-hemiplegia-epilepsy syndrome: early magnetic resonance imaging findings and neuroradiological follow-upI Toldo, M Calderone, C Boniver, et al.Pageof 483