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Brain & Development|April 14, 2025
Synaptic disturbance in neurodevelopmental disorders: Perspectives from fragile X and Rett syndromesRuixiang Li, Mai Anzai, Akiko Shibata, et al.Pediatrics International : Official Journal of the Japan Pediatric Society|December 17, 2018
Prolonged mild disturbance of consciousness and acute encephalopathyKeita Kanamori, Hiroshi Terashima, Mai Anzai, et al.Brain & Development|May 12, 2016
First Japanese variant of late infantile neuronal ceroid lipofuscinosis caused by novel CLN6 mutationsRyo Sato, Takehiko Inui, Wakaba Endo, et al.Pediatrics International : Official Journal of the Japan Pediatric Society|September 1, 2016
Patchy white matter hyperintensity in ring chromosome 18 syndromeMai Anzai, Natsuko Arai-Ichinoi, Yusuke Takezawa, et al.Brain & Development|October 3, 2015
Outcome of hemiplegic cerebral palsy born at term depends on its etiologyYukihiro Kitai, Kazuhiro Haginoya, Satori Hirai, et al.Journal of Human Genetics|February 3, 2017
A novel mutation in the proteolytic domain of LONP1 causes atypical CODAS syndromeTakehiko Inui, Mai Anzai, Yusuke Takezawa, et al.Brain & Development|May 29, 2017
A patient with Muenke syndrome manifesting migrating neonatal seizuresYukimune Okubo, Taro Kitamura, Mai Anzai, et al.Journal of the Neurological Sciences|March 6, 2016
FDG-PET study of patients with Leigh syndromeKauzhiro Haginoya, Tomohiro Kaneta, Noriko Togashi, et al.Journal of Human Genetics|March 8, 2019
Leucine-485 deletion variant of BRAF may exhibit the severe end of the clinical spectrum of CFC syndromeSato Suzuki-Muromoto, Takuya Miyabayashi, Koki Nagai, et al.Annals of Clinical and Translational Neurology|May 16, 2018
Genomic analysis identifies masqueraders of full-term cerebral palsyYusuke Takezawa, Atsuo Kikuchi, Kazuhiro Haginoya, et al.Pageof 1