Comparative characterization of PCDH19 missense and truncating variants in PCDH19-related epilepsy
Shibata, Mami, Ishii, Atsushi, Goto, Ayako, Hirose, Shinichi
Published in Journal of human genetics (01.06.2021)
Published in Journal of human genetics (01.06.2021)
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Neuroanatomical considerations for optimizing thalamic deep brain stimulation in Tourette syndrome
Morishita, Takashi, Sakai, Yuki, Iida, Hitoshi, Yoshimura, Saki, Ishii, Atsushi, Fujioka, Shinsuke, Tanaka, Saori C, Inoue, Tooru
Published in Journal of neurosurgery (01.01.2022)
Published in Journal of neurosurgery (01.01.2022)
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Epidemiological changes of acute encephalopathy in Japan based on national surveillance for 2014–2017
Kasai, Mariko, Shibata, Akiko, Hoshino, Ai, Maegaki, Yoshihiro, Yamanouchi, Hideo, Takanashi, Jun-ichi, Yamagata, Takanori, Sakuma, Hiroshi, Okumura, Akihisa, Nagase, Hiroaki, Ishii, Atsushi, Goto, Tomohide, Oka, Akira, Mizuguchi, Masashi
Published in Brain & development (Tokyo. 1979) (01.08.2020)
Published in Brain & development (Tokyo. 1979) (01.08.2020)
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Application of induced pluripotent stem cells in epilepsy
Hirose, Shinichi, Tanaka, Yasuyoshi, Shibata, Mami, Kimura, Yuichi, Ishikawa, Mitsuru, Higurashi, Norimichi, Yamamoto, Toshiyuki, Ichise, Eisuke, Chiyonobu, Tomohiro, Ishii, Atsushi
Published in Molecular and cellular neuroscience (01.10.2020)
Published in Molecular and cellular neuroscience (01.10.2020)
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CUX2 deficiency causes facilitation of excitatory synaptic transmission onto hippocampus and increased seizure susceptibility to kainate
Suzuki, Toshimitsu, Tatsukawa, Tetsuya, Sudo, Genki, Delandre, Caroline, Pai, Yun Jin, Miyamoto, Hiroyuki, Raveau, Matthieu, Shimohata, Atsushi, Ohmori, Iori, Hamano, Shin-Ichiro, Haginoya, Kazuhiro, Uematsu, Mitsugu, Takahashi, Yukitoshi, Morimoto, Masafumi, Fujimoto, Shinji, Osaka, Hitoshi, Oguni, Hirokazu, Osawa, Makiko, Ishii, Atsushi, Hirose, Shinichi, Kaneko, Sunao, Inoue, Yushi, Moore, Adrian Walton, Yamakawa, Kazuhiro
Published in Scientific reports (17.05.2022)
Published in Scientific reports (17.05.2022)
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SCN8A encephalopathy: Research progress and prospects
Meisler, Miriam H., Helman, Guy, Hammer, Michael F., Fureman, Brandy E., Gaillard, William D., Goldin, Alan L., Hirose, Shinichi, Ishii, Atsushi, Kroner, Barbara L., Lossin, Christoph, Mefford, Heather C., Parent, Jack M., Patel, Manoj, Schreiber, John, Stewart, Randall, Whittemore, Vicky, Wilcox, Karen, Wagnon, Jacy L, Pearl, Phillip L., Vanderver, Adeline, Scheffer, Ingrid E.
Published in Epilepsia (Copenhagen) (01.07.2016)
Published in Epilepsia (Copenhagen) (01.07.2016)
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New directions in earth system governance research
Burch, Sarah, Gupta, Aarti, Inoue, Cristina Y.A., Kalfagianni, Agni, Persson, Åsa, Gerlak, Andrea K., Ishii, Atsushi, Patterson, James, Pickering, Jonathan, Scobie, Michelle, Van der Heijden, Jeroen, Vervoort, Joost, Adler, Carolina, Bloomfield, Michael, Djalante, Riyanti, Dryzek, John, Galaz, Victor, Gordon, Christopher, Harmon, Renée, Jinnah, Sikina, Kim, Rakhyun E., Olsson, Lennart, Van Leeuwen, Judith, Ramasar, Vasna, Wapner, Paul, Zondervan, Ruben
Published in Earth system governance (01.01.2019)
Published in Earth system governance (01.01.2019)
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Identification of ATP1A3 mutations by exome sequencing as the cause of alternating hemiplegia of childhood in Japanese patients
Ishii, Atsushi, Saito, Yoshiaki, Mitsui, Jun, Ishiura, Hiroyuki, Yoshimura, Jun, Arai, Hidee, Yamashita, Sumimasa, Kimura, Sadami, Oguni, Hirokazu, Morishita, Shinichi, Tsuji, Shoji, Sasaki, Masayuki, Hirose, Shinichi
Published in PloS one (08.02.2013)
Published in PloS one (08.02.2013)
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Copy number variation analysis in 83 children with early-onset developmental and epileptic encephalopathy after targeted resequencing of a 109-epilepsy gene panel
Hirabayashi, Kyoko, Uehara, Daniela Tiaki, Abe, Hidetoshi, Ishii, Atsushi, Moriyama, Keiji, Hirose, Shinichi, Inazawa, Johji
Published in Journal of human genetics (01.11.2019)
Published in Journal of human genetics (01.11.2019)
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