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Epilepsia|December 15, 2024
Girdin deficiency causes developmental and epileptic encephalopathy with hippocampal sclerosis and interneuronopathyMachiko Iida, Motoki Tanaka, Tsuyoshi Takagi, et al.Journal of Human Genetics|January 13, 2017
PARS2 and NARS2 mutations in infantile-onset neurodegenerative disorderTakeshi Mizuguchi, Mitsuko Nakashima, Mitsuhiro Kato, et al.Scientific Reports|October 21, 2024
Identifying pathogenic variants in rare pediatric neurological diseases using exome sequencingKazuyuki Komatsu, Mitsuhiro Kato, Kazuo Kubota, et al.Brain & Development|April 2, 2016
The effects of co-medications on lamotrigine clearance in Japanese children with epilepsyTomoya Takeuchi, Jun Natsume, Hiroyuki Kidokoro, et al.Science Advances|November 5, 2025
Landscape-wide cosmogram built by the early community of Aguada Fénix in southeastern MesoamericaTakeshi Inomata, Daniela Triadan, Verónica A Vázquez López, et al.Epilepsia Open|June 7, 2021
Efficacy of long-term adrenocorticotropic hormone therapy for West syndrome: A retrospective multicenter case seriesShimpei Baba, Tohru Okanishi, Yoichiro Homma, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 28, 2022
Genetic and clinical landscape of childhood cerebellar hypoplasia and atrophyMasamune Sakamoto, Kazuhiro Iwama, Masayuki Sasaki, et al.Pageof 4