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Brain & Development|October 27, 2025
Etiology-specific diagnosis of cytotoxic lesions of the corpus callosum (CLOCC) in a single-center pediatric cohort: diagnostic challenges and outcome characteristicsYavuz Ataş, Cenk Eraslan, Tuğce Ince, et al.Brain & Development|October 17, 2025
Associations between cerebrospinal fluid pressure levels, clinical features, and MRI abnormalities in pediatric idiopathic intracranial hypertension: A retrospective studyHasan Emral, Tülay Kamaşak, İlker Eyüboğlu, et al.Brain & Development|September 12, 2025
Examination of brain morphology and perinatal background factors associated with characteristics of early infantile spontaneous movementsNanae Kawano, Tomoki Maeda, Osamu Kobayashi, et al.Brain & Development|August 10, 2025
Cancers in an aging population with severe motor and intellectual disabilities: a single-center retrospective cohort studyHiroshi Terashima, Yoshiaki Saito, Nagahisa Takahashi, et al.Brain & Development|February 16, 2026
Clinical profiles of tuberous sclerosis complex: A regionally based surveyMisae Yamada, Jun Natsume, Yuki Maki, et al.Brain & Development|June 24, 2025
Hand-arm bimanual intensive therapy versus modified constraint-induced movement therapy in children with hemiparetic cerebral palsy: A randomized controlled trialPrateek Kumar Panda, Indar Kumar Sharawat, Diksha Gupta, et al.Brain & Development|March 31, 2025
COVID-19 infection and vaccination in children with Dravet syndrome or infantile epileptic spasms syndrome: An internet survey in JapanSusumu Ito, Aiko Nishikawa, Ruby Kuroiwa, et al.Brain & Development|March 31, 2025
A case of spinal muscular atrophy type 0 treated with nusinersen without progression of early-onset scoliosis - possibility of preventing scoliosis with a rehabilitation program focusing on postural managementTomokazu Kimizu, Saki Yokawa, Takuya Horibe, et al.Brain & Development|April 1, 2025
Brown-Vialetto-Van Laere syndrome patients with unusual phenotypes from Indian ethnicity: Functional analysis of clinical variants in SLC52A2 and SLC52A3 genesSanthalingam Gayathri, Manikka Kubendran Aravind, Vykuntaraju K Gowda, et al.Pageof 482