Mutation in the STXBP1 Gene Associated with Early Onset West Syndrome: A Case Report and Literature Review

por Takeda, Kanako, Miyamoto, Yusaku, Yamamoto, Hisako, Iwasaki, Toshiyuki, Sumitomo, Noriko, Takeshita, Eri, Ishii, Atsushi, Hirose, Shinichi, Shimizu, Naoki
Publicado 2022

ATP1A3 variants and slowly progressive cerebellar ataxia without paroxysmal or episodic symptoms in children

por Sasaki, Masayuki, Sumitomo, Noriko, Shimizu‐Motohashi, Yuko, Takeshita, Eri, Kurosawa, Kenji, Kosaki, Kenjiro, Iwama, Kazuhiro, Mizuguchi, Takeshi, Matsumoto, Naomichi
Publicado 2020

Low EEG Gamma Entropy and Glucose Hypometabolism After Corpus Callosotomy Predicts Seizure Outcome After Subsequent Surgery

por Kosugi, Kenzo, Iijima, Keiya, Yokosako, Suguru, Takayama, Yutaro, Kimura, Yuiko, Kaneko, Yuu, Sumitomo, Noriko, Saito, Takashi, Nakagawa, Eiji, Sato, Noriko, Iwasaki, Masaki
Publicado 2022

Corpus callosotomy in pediatric patients with non-lesional epileptic encephalopathy with electrical status epilepticus during sleep

por Yokosako, Suguru, Muraoka, Norihiro, Watanabe, Shiena, Kosugi, Kenzo, Takayama, Yutaro, Iijima, Keiya, Kimura, Yuiko, Kaneko, Yu, Sumitomo, Noriko, Saito, Takashi, Nakagawa, Eiji, Iwasaki, Masaki
Publicado 2021

Novel TK2 mutations as a cause of delayed muscle maturation in mtDNA depletion syndrome

por Termglinchan, Thanes, Hisamatsu, Seito, Ohmori, Junko, Suzumura, Hiroshi, Sumitomo, Noriko, Imataka, George, Arisaka, Osamu, Murakami, Nobuyuki, Minami, Narihiro, Akihiko, Ishiyama, Sasaki, Masayuki, Goto, Yuichi, Noguchi, Satoru, Nonaka, Ikuya, Mitsuhashi, Satomi, Nishino, Ichizo
Publicado 2016