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Brain & Development|September 20, 2016
A novel homozygous HOXB1 mutation in a Turkish family with hereditary congenital facial paresisYavuz Sahin, Olcay Güngör, Akif Ayaz, et al.Brain & Development|September 26, 2016
Muscle development in healthy children evaluated by bioelectrical impedance analysisTomoka Uchiyama, Takahiro Nakayama, Satoshi KuruBrain & Development|April 26, 2017
The effect of dietary supplements on clinical aspects of autism spectrum disorder: A systematic review of the literatureMaria Gogou, George KoliosBrain & Development|March 2, 2010
Three-year-old child with meroacrania - neurological signsCarolina Araújo Rodrigues Funayama, Luzia Iara Pfeifer, Ester Silveira Ramos, et al.Brain & Development|September 27, 2016
Determination of restless legs syndrome prevalence in children aged 13-16years in the provincial center of KayseriHuseyin Per, Neslihan Gunay, Sevda Ismailogullari, et al.Brain & Development|June 21, 2017
Novel FKRP mutations in a Japanese MDC1C sibship clinically diagnosed with Fukuyama congenital muscular dystrophyMieko Yoshioka, Kazuhiro Kobayashi, Tatsushi TodaBrain & Development|May 13, 2017
The characteristics of salivary pepsin in patients with severe motor and intellectual disabilitiesNaoki Hashizume, Suguru Fukahori, Kimio Asagiri, et al.Brain & Development|June 12, 2017
Relationships between long-term observations of motor milestones and genotype analysis results in childhood-onset Japanese spinal muscular atrophy patientsKaori Kaneko, Reiko Arakawa, Mari Urano, et al.Brain & Development|October 24, 2009
Epileptic encephalopathy in children possibly related to immune-mediated pathogenesisNicola Specchio, Lucia Fusco, Dianela Claps, et al.Brain & Development|October 27, 2009
Behavioral improvement after transplantation of neural precursors derived from embryonic stem cells into the globally ischemic brain of adolescent ratsHoon-Chul Kang, Dae-Sung Kim, Ji Young Kim, et al.Pageof 482