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Epilepsy & Behavior : E&B|August 8, 2020
Evaluation of interobserver variability in application of the new neonatal seizure classification proposed by the ILAE Task ForceTetsuo Kubota, Hiroyuki Kidokoro, Sho Narahara, et al.
Rinsho Shinkeigaku = Clinical Neurology|August 5, 2014
[Beneficial effects of 3,4-diaminopyridine in a 26-year-old woman with DOK7 congenital myasthenic syndrome who was originally diagnosed with facioscapulohumeral dystrophy]Atsuko Nishikawa, Madoka Mori-Yoshimura, Tomoko Okamoto, et al.
Annals of Clinical and Translational Neurology|March 9, 2023
Impaired gating of γ- and ε-AChR respectively causes Escobar syndrome and fast-channel myastheniaXin-Ming Shen, Tomohiko Nakata, Seiji Mizuno, et al.
Brain & Development|July 22, 2008
Callosal lesions and delirious behavior during febrile illnessAkihisa Okumura, Fumio Hayakawa, Toru Kato, et al.
IEEE Journal of Biomedical and Health Informatics|December 22, 2025
Prediction of Long-term Prognosis in Infantile Epileptic Spasms Syndrome of Unknown Etiology based on Hypsarrhythmia by Self-Attention AutoencoderRyosuke Suzui, Jun Natsume, Masahiro Kawaguchi, et al.
Journal of Infection and Chemotherapy : Official Journal of the Japan Society of Chemotherapy|February 6, 2016
Recurrent bacteremia with different strains of Streptococcus pyogenes in an immunocompromised childTakuya Hattori, Masaaki Minami, Kotaro Narita, et al.
No to Hattatsu = Brain and Development|December 18, 2012
[Clinical features of congenital myasthenic syndrome in Japan]Kaori Irahara, Hirofumi Komaki, Ryoko Honda, et al.
Brain & Development|December 16, 2019
Novel biallelic FA2H mutations in a Japanese boy with fatty acid hydroxylase-associated neurodegenerationMasahiro Kawaguchi, Takayuki Sassa, Hiroyuki Kidokoro, et al.
Brain & Development|August 1, 2024
Epileptic foci and networks in children with epilepsy after acute encephalopathy with biphasic seizures and late reduced diffusionTakamasa Mitsumatsu, Yuji Ito, Yuki Maki, et al.
Human Mutation|April 5, 2013
Mutations in the C-terminal domain of ColQ in endplate acetylcholinesterase deficiency compromise ColQ-MuSK interactionTomohiko Nakata, Mikako Ito, Yoshiteru Azuma, et al.
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