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Brain & Development|August 23, 2025
Gene therapy for Duchenne muscular dystrophyYuko Shimizu-MotohashiBrain & Development|August 26, 2025
Recognizing ataxia requiring intervention: a retrospective cohort study of poor prognostic factors in pediatric emergency department patientsTsuyoshi Aihara, Shunsuke Amagasa, Itaru Hayakawa, et al.Brain & Development|January 1, 1984
Arthrogryposis multiplex congenita in an infant with posterior agenesis of the corpus callosumT M Voorhies, R D Nass, V J VigoritaBrain & Development|August 25, 2016
A Japanese case of β-ureidopropionase deficiency with dysmorphic featuresTomoyuki Akiyama, Takashi Shibata, Harumi Yoshinaga, et al.Brain & Development|April 20, 2021
Morphometric analysis of spike-wave complexes (SWCs) causing myoclonic seizures in children with idiopathic myoclonic epilepsies - A positive SWC component correlates with myoclonic intensityHirokazu Oguni, Susumu Ito, Aiko Nishikawa, et al.Brain & Development|June 3, 2014
Menkes disease in Korea: ATP7A mutation and epilepsy phenotypeJin Sook Lee, Byung Chan Lim, Ki Joong Kim, et al.Brain & Development|January 1, 1986
Stroke in a patient with hemolytic-uremic syndrome with a good outcomeA Steinberg, M Ish-Horowitcz, O el-Peleg, et al.Brain & Development|January 1, 1986
Increased cadmium resistance of skin fibroblasts from Menkes disease patientsA Hayashi, M Sato, M Arima, et al.Brain & Development|January 25, 2026
A lipidation inhibitor rescues impaired neurite outgrowth caused by the CDC42 mutation associated with Takenouchi-Kosaki syndrome in Neuro2A cellsEtsuko Daimon, Yukinao Shibukawa, Natsuko Yamazaki, et al.Brain & Development|January 1, 1985
Short latency somatosensory evoked potentials to peroneal nerve stimulation in normal Japanese childrenT Hashimoto, M Tayama, K Fukuda, et al.Pageof 483