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Epilepsia|June 6, 2019
Hippocampal diffusion abnormality after febrile status epilepticus is related to subsequent epilepsySetsuri Yokoi, Hiroyuki Kidokoro, Hiroyuki Yamamoto, et al.
American Journal of Medical Genetics. Part A|November 21, 2012
Clinical and radiological features of Japanese patients with a severe phenotype due to CASK mutationsJun-ichi Takanashi, Nobuhiko Okamoto, Yuto Yamamoto, et al.
Epilepsy & Behavior : E&B|April 10, 2021
Risks of ACTH therapy for West syndrome following BCG vaccinationYuki Maki, Jun Natsume, Ikumi Hori, et al.
Neurology. Genetics|December 17, 2025
Identification of Intronic Variants in NDUFA3 as a Cause of Leigh Syndrome by Whole Genome Sequencing and RNA SequencingKohta Nakamura, Yoshihito Kishita, Ayumu Sugiura, et al.
Journal of the Peripheral Nervous System : JPNS|June 30, 2017
Clinical and genetic diversities of Charcot-Marie-Tooth disease with MFN2 mutations in a large case studyMasahiro Ando, Akihiro Hashiguchi, Yuji Okamoto, et al.
Brain : a Journal of Neurology|September 27, 2018
De novo PHACTR1 mutations in West syndrome and their pathophysiological effectsNanako Hamada, Shunsuke Ogaya, Mitsuko Nakashima, et al.
Developmental Medicine and Child Neurology|October 31, 2014
Clinical and genetic investigation of 17 Japanese patients with hyperekplexiaJun Mine, Takeshi Taketani, Kazushi Yoshida, 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.
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