Progress in searching for the febrile seizure susceptibility genes von Nakayama, Junko

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Anesthetic management of super-elderly patients with remimazolam: a report of two cases von Nakayama, Junko, Ogihara, Tomomi, Yajima, Rui, Innami, Yasushi, Ouchi, Takashi

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Robot-assisted training using Hybrid Assistive Limb® for cerebral palsy von Matsuda, Mayumi, Iwasaki, Nobuaki, Mataki, Yuki, Mutsuzaki, Hirotaka, Yoshikawa, Kenichi, Takahashi, Kazushi, Enomoto, Keiko, Sano, Kumiko, Kubota, Aoi, Nakayama, Tomohiro, Nakayama, Junko, Ohguro, Haruka, Mizukami, Masafumi, Tomita, Kazuhide

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Longitudinal, prospective study of head impacts in male high school football players von McAlister, Kelsey L, Mack, Wendy J, Bir, Cynthia, Baron, David A, Som, Christine, Li, Karen, Chavarria-Garcia, Anthony, Sawardekar, Siddhant, Baron, David, Toth, Zachary, Allem, Courtney, Beatty, Nicholas, Nakayama, Junko, Kelln, Ryan, Zaslow, Tracy, Bansal, Ravi, Peterson, Bradley S

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Benefits of a Wearable Cyborg HAL (Hybrid Assistive Limb) in Patients with Childhood-Onset Motor Disabilities: A 1-Year Follow-Up Study von Kuroda, Mayumi Matsuda, Iwasaki, Nobuaki, Mutsuzaki, Hirotaka, Yoshikawa, Kenichi, Takahashi, Kazushi, Nakayama, Tomohiro, Nakayama, Junko, Takeuchi, Ryoko, Mataki, Yuki, Ohguro, Haruka, Tomita, Kazuhide

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Task-specific enhancement of hippocampus-dependent learning in mice deficient in monoacylglycerol lipase, the major hydrolyzing enzyme of the endocannabinoid 2-arachidonoylglycerol von Kishimoto, Yasushi, Cagniard, Barbara, Yamazaki, Maya, Nakayama, Junko, Sakimura, Kenji, Kirino, Yutaka, Kano, Masanobu

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Abnormal brain MRI signal in 18q-syndrome not due to dysmyelination von Tanaka, Ryuta, Iwasaki, Nobuaki, Hayashi, Masaharu, Nakayama, Junko, Ohto, Tatsuyuki, Takahashi, Miho, Numano, Tomokazu, Homma, Kazuhiro, Hamano, Kenzo, Sumazaki, Ryo

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A Japanese case of ichthyosis follicularis with atrichia and photophobia syndrome with an MBTPS2 mutation von Nakayama, Junko, Iwasaki, Nobuaki, Shin, Kenji, Sato, Hideo, Kamo, Mariko, Ohyama, Manabu, Noguchi, Emiko, Arinami, Tadao

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Molecular genetics of febrile seizures von Nakayama, Junko, Arinami, Tadao

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Inhibition of fatty achid amide hydrolase accelerates acquisition of cerebellum-dependent eyeblink conditioning von Nakayama, Junko, Oku, Ikuko, Kirino, Yutaka, Kishimoto, Yasushi

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Possible association between a haplotype of the GABA-A receptor alpha 1 subunit gene ( GABRA1) and mood disorders von Horiuchi, Yasue, Nakayama, Junko, Ishiguro, Hiroki, Ohtsuki, Tsuyuka, Detera-Wadleigh, Sevilla D, Toyota, Tomoko, Yamada, Kazuo, Nankai, Masahiro, Shibuya, Haruo, Yoshikawa, Takeo, Arinami, Tadao

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Voluntary-assisted Upper Limb Training for Severe Cerebral Palsy Using Robotics Devices and Neuromuscular Electrical Stimulation: Three Case Reports von Kuroda, Mayumi Matsuda, Iwasaki, Nobuaki, Yoshikawa, Kenichi, Takeuchi, Ryoko, Mataki, Yuki, Nakayama, Tomohiro, Nakayama, Junko, Ohguro, Haruka, Tokeji, Kayo, Mutsuzaki, Hirotaka

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Crosslinking of near responses in healthy young subjects von Asakawa, Ken, Tomioka, Maho, Nakayama, Junko, Hayama, Mayu, Hinata, Miki, Ishikawa, Hitoshi

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A Patient with Rett Syndrome Maintained Motor Function by Periodic Rehabilitation Therapy and Proactive Daily Activities von Imamura, Tsuyoshi, Nakayama, Tomohiro, Nakayama, Junko, Iwasaki, Nobuaki

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Monozygotic twins with de novo ZIC2 gene mutations discordant for the type of holoprosencephaly von Nakayama, Junko, Kinugasa, Hideyo, Ohto, Tatsuyuki, Tanaka, Ryuta, Nakayama, Tomohiro, Noguchi, Emiko, Arinami, Tadao, Iwasaki, Nobuaki

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Significant linkage to chromosome 22q for exploratory eye movement dysfunction in schizophrenia von Takahashi, Sakae, Ohtsuki, Tsuyuka, Yu, Shun-Ying, Tanabe, Ei-ichi, Yara, Kazuo, Kamioka, Masashi, Matsushima, Eisuke, Matsuura, Masato, Ishikawa, Koichi, Minowa, Yousuke, Noguchi, Emiko, Nakayama, Junko, Yamakawa-Kobayashi, Kimiko, Arinami, Tadao, Kojima, Takuya

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Failure to find causal mutations in the GABAA-receptor γ2 subunit (GABRG2) gene in Japanese febrile seizure patients von NAKAYAMA, Junko, HAMANO, Kenzo, NOGUCHI, Emiko, HORIUCHI, Yasue, IWASAKI, Nobuaki, OHTA, Masayasu, NAKAHARA, Satoko, NAOI, Takayuki, MATSUI, Akira, ARINAMI, Tadao

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Failure to find evidence for association between voltage-gated sodium channel gene SCN2A variants and febrile seizures in humans von Nakayama, Junko, Yamamoto, Nao, Hamano, Kenzo, Iwasaki, Nobuaki, Ohta, Masayasu, Nakahara, Satoko, Horigome, Yumi, Nakahara, Chieko, Noguchi, Emiko, Shiono, Junko, Shimakura, Yae, Yamakawa-Kobayashi, Kimiko, Matsui, Akira, Arinami, Tadao

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Family-based association study of the NOTCH4 gene in schizophrenia using Japanese and Chinese samples von Takahashi, Sakae, Cui, Yu-hu, Kojima, Takuya, Han, Yong-hua, Yu, Shun-ying, Tanabe, Eiici, Yara, Kazuo, Matsuura, Masato, Matsushima, Eisuyke, Nakayama, Junko, Arinami, Tadao, Shen, Yu-cun, Faraone, Stephen V, Tsuang, Ming T

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A novel homozygous mutation of GJC2 derived from maternal uniparental disomy in a female patient with Pelizaeus–Merzbacher-like disease von Shimojima, Keiko, Tanaka, Ryuta, Shimada, Shino, Sangu, Noriko, Nakayama, Junko, Iwasaki, Nobuaki, Yamamoto, Toshiyuki

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