Showing results (81-90 of 100) with videos related to
Sort By:
Pageof 10
Orphanet Journal of Rare Diseases|January 7, 2021
Acute encephalopathy in children with tuberous sclerosis complexShingo Numoto, Hirokazu Kurahashi, Atsushi Sato, et al.Journal of Neurosurgery. Pediatrics|July 31, 2023
Disconnection surgery to cure or palliate medically intractable epileptic spasms: a retrospective studySaya Koh, Takehiro Uda, Noritsugu Kunihiro, et al.Brain Sciences|February 27, 2026
Lower Interhemispheric Coherence in Adults with Surgically Treated Severe Generalized Epilepsy than in Patients Without Epilepsy: A Scalp EEG StudyShugo Nishijima, Takehiro Uda, Vich Yindeedej, et al.Acta Neuropathologica|May 7, 2008
Aristaless-related homeobox gene disruption leads to abnormal distribution of GABAergic interneurons in human neocortex: evidence based on a case of X-linked lissencephaly with abnormal genitalia (XLAG)Shin Okazaki, Maki Ohsawa, Ichiro Kuki, et al.Journal of Human Genetics|January 23, 2015
Detecting copy-number variations in whole-exome sequencing data using the eXome Hidden Markov Model: an 'exome-first' approachSatoko Miyatake, Eriko Koshimizu, Atsushi Fujita, et al.Brain & Development|September 1, 2016
Quinidine therapy for West syndrome with KCNTI mutation: A case reportMasataka Fukuoka, Ichiro Kuki, Hisashi Kawawaki, et al.Journal of Neurosurgery. Pediatrics|February 26, 2021
Phase-amplitude coupling of interictal fast activities modulated by slow waves on scalp EEG and its correlation with seizure outcomes of disconnection surgery in children with intractable nonlesional epileptic spasmsTakehiro Uda, Ichiro Kuki, Takeshi Inoue, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 21, 2024
Evidence-based diagnostic prediction score for pediatric NMDA receptor encephalitisShimpei Matsuda, Takayuki Mori, Mariko Kasai, et al.Annals of Clinical and Translational Neurology|February 23, 2021
gAChR antibodies in children and adolescents with acquired autoimmune dysautonomia in JapanMakoto Yamakawa, Mari Watari, Ken-Ichi Torii, et al.Brain & Development|July 29, 2019
Thermolabile polymorphism of carnitine palmitoyltransferase 2: A genetic risk factor of overall acute encephalopathyAkiko Shibata, Mariko Kasai, Ai Hoshino, et al.Pageof 10