Mutations of Neuronal Voltage‐gated Na+ Channel α1 Subunit Gene SCN1A in Core Severe Myoclonic Epilepsy in Infancy (SMEI) and in Borderline SMEI (SMEB) von Fukuma, Goryu, Oguni, Hirokazu, Shirasaka, Yukiyoshi, Watanabe, Kazuyoshi, Miyajima, Tasuku, Yasumoto, Sawa, Ohfu, Masaharu, Inoue, Takahito, Watanachai, Aruchalean, Kira, Ryutaro, Matsuo, Muneaki, Muranaka, Hideki, Sofue, Fumiko, Zhang, Bo, Kaneko, Sunao, Mitsudome, Akihisa, Hirose, Shinichi

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PCDH19 -related female-limited epilepsy: Further details regarding early clinical features and therapeutic efficacy von Higurashi, Norimichi, Nakamura, Mai, Sugai, Misaki, Ohfu, Masaharu, Sakauchi, Masako, Sugawara, Yuji, Nakamura, Kazuyuki, Kato, Mitsuhiro, Usui, Daisuke, Mogami, Yukiko, Fujiwara, Yumi, Ito, Tomoshiro, Ikeda, Hiroko, Imai, Katsumi, Takahashi, Yukitoshi, Nukui, Megumi, Inoue, Takeshi, Okazaki, Shin, Kirino, Tomoko, Tomonoh, Yuko, Inoue, Takahito, Takano, Kyoko, Shimakawa, Shuichi, Hirose, Shinichi

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Microchromosomal deletions involving SCN1A and adjacent genes in severe myoclonic epilepsy in infancy von Wang, Ji‐wen, Kurahashi, Hirokazu, Ishii, Atsushi, Kojima, Toshio, Ohfu, Masaharu, Inoue, Takahito, Ogawa, Atsushi, Yasumoto, Sawa, Oguni, Hirokazu, Kure, Shigeo, Fujii, Tatsuya, Ito, Masatoshi, Okuno, Takehiko, Shirasaka, Yukiyoshi, Natsume, Jun, Hasegawa, Aki, Konagaya, Akihiko, Kaneko, Sunao, Hirose, Shinichi

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Clinical spectrum of SCN2A mutations expanding to Ohtahara syndrome von Nakamura, Kazuyuki, Kato, Mitsuhiro, Osaka, Hitoshi, Yamashita, Sumimasa, Nakagawa, Eiji, Haginoya, Kazuhiro, Tohyama, Jun, Okuda, Mitsuko, Wada, Takahito, Shimakawa, Shuichi, Imai, Katsumi, Takeshita, Saoko, Ishiwata, Hisako, Lev, Dorit, Lerman-Sagie, Tally, Cervantes-Barragán, David E., Villarroel, Camilo E., Ohfu, Masaharu, Writzl, Karin, Gnidovec Stražišar, Barbara, Hirabayashi, Shinichi, Chitayat, David, Myles Reid, Diane, Nishiyama, Kiyomi, Kodera, Hirofumi, Nakashima, Mitsuko, Tsurusaki, Yoshinori, Miyake, Noriko, Hayasaka, Kiyoshi, Matsumoto, Naomichi, Saitsu, Hirotomo

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Appearance of focal cortical dysplasia on serial MRI after maturation of myelination von Yoshida, Fumiaki, Morioka, Takato, Hashiguchi, Kimiaki, Miyagi, Yasushi, Nagata, Shinji, Yamaguchi, Yui, Ohfu, Masaharu, Sasaki, Tomio

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Immediate suppression of seizure clusters by corticosteroids in PCDH19 female epilepsy von Higurashi, Norimichi, Takahashi, Yukitoshi, Kashimada, Ayako, Sugawara, Yuji, Sakuma, Hiroshi, Tomonoh, Yuko, Inoue, Takahito, Hoshina, Megumi, Satomi, Ruri, Ohfu, Masaharu, Itomi, Kazuya, Takano, Kyoko, Kirino, Tomoko, Hirose, Shinichi

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Rapid and sensitive detection of urinary 4-hydroxybutyric acid and its related compounds by gas chromatography–mass spectrometry in a patient with succinic semialdehyde dehydrogena... von Shinka, Toshihiro, Inoue, Yoshito, Ohse, Morimasa, Ito, Akira, Ohfu, Masaharu, Hirose, Shinichi, Kuhara, Tomiko

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Mutations of neuronal voltage-gated Na+ channel alpha 1 subunit gene SCN1A in core severe myoclonic epilepsy in infancy (SMEI) and in borderline SMEI (SMEB) von Fukuma, Goryu, Oguni, Hirokazu, Shirasaka, Yukiyoshi, Watanabe, Kazuyoshi, Miyajima, Tasuku, Yasumoto, Sawa, Ohfu, Masaharu, Inoue, Takahito, Watanachai, Aruchalean, Kira, Ryutaro, Matsuo, Muneaki, Muranaka, Hideki, Sofue, Fumiko, Zhang, Bo, Kaneko, Sunao, Mitsudome, Akihisa, Hirose, Shinichi

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The effectiveness of clonazepam on the rolandic discharges von Mitsudome, Akihisa, Ohfu, Masaharu, Yasumoto, Sawa, Ogawa, Atsushi, Hirosea, Shinichi, Ogata, Hiroko, Yamada, Thoru

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Application of rapid random stimulation (RRS) to visual evoked potentials in children von Fujikawa, Maiko, Ohfu, Masaharu, Fujikawa, Sadatoshi, Chen, Tsau-Tsen, Mitsudome, Akihisa

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Diagnosis of epilepsy using an implantable loop recorder in a child with long-QT syndrome type 3 von Takahashi, Kazuhiro, Miyake, Akira, Otsuka, Yoshimitsu, Ohfu, Masaharu, Ganaha, Hitoshi

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PS-39-5 High amplitude somatosensory evoked potentials in children with midline spikes on EEG von Ohfu, Masaharu, Mitsudome, Akihisa

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