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Brain & Development|December 22, 2015
Clinical and allelic heterogeneity in a pediatric cohort of 11 patients carrying MFN2 mutationChloé Di Meglio, Nathalie Bonello-Palot, Christophe Boulay, et al.Brain & Development|December 22, 2015
Surgical versus medical treatment for children with epileptic encephalopathy in infancy and early childhood: Results of an international multicenter cohort study in Far-East Asia (the FACE study)Taisuke Otsuki, Heung-Dong Kim, Guoming Luan, et al.Brain & Development|January 23, 2016
Successful treatment of migrating partial seizures in Wolf-Hirschhorn syndrome with bromideAyako Itakura, Yoshiaki Saito, Yoko Nishimura, et al.Brain & Development|May 15, 2016
Clinical and genetic analysis of two Chinese infants with Mabry syndromeJiao Xue, Hui Li, Yuehua Zhang, et al.Brain & Development|May 18, 2016
A novel gene mutation in PANK2 in a patient with severe jaw-opening dystoniaZuhal Yapici, Nihan Hande Akcakaya, Pinar Tekturk, et al.Brain & Development|March 24, 2016
Stem cells therapy in cerebral palsy: A systematic reviewAgnieszka Kułak-Bejda, Piotr Kułak, Grzegorz Bejda, et al.Brain & Development|February 13, 2016
Temple syndrome: A patient with maternal hetero-UPD14, mixed iso- and hetero-disomy detected by SNP microarray typing of patient-father duosEun-Hye Shin, Eunhae Cho, Cha Gon LeeBrain & Development|February 13, 2016
Electroclinical phenotype in Rubinstein-Taybi syndromeAntonella Giacobbe, Paola Francesca Ajmone, Donatella Milani, et al.Brain & Development|May 12, 2016
Reversible cerebral vasoconstriction syndrome manifesting as focal seizures without a thunderclap headache: A pediatric case reportShuji Kuga, Hironori Goto, Kazuo Okanari, et al.Brain & Development|January 1, 1989
Immunohistochemical dystrophin reaction in synaptic regionsT Miike, M Miyatake, J Zhao, et al.Pageof 478