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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Genetic analysis of PRRT2 for benign infantile epilepsy, infantile convulsions with choreoathetosis syndrome, and benign convulsions with mild gastroenteritis von Ishii, Atsushi, Yasumoto, Sawa, Ihara, Yukiko, Inoue, Takahito, Fujita, Takako, Nakamura, Noriko, Ohfu, Masaharu, Yamashita, Yushiro, Takatsuka, Hideo, Taga, Toshiaki, Miyata, Rie, Ito, Masahiro, Tsuchiya, Hiroshi, Matsuoka, Taro, Kitao, Tetsuya, Murakami, Kiyotaka, Lee, Wang-Tso, Kaneko, Sunao, Hirose, Shinichi

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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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P2-118. Clinical electroencephalographic study in ten cases with Posterior Reversible Encephalopathy Syndrome (PRES) von Ohfu, Masaharu, Matsuoka, Tsuyoshi, Hiyane, Masato

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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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A Case of Mild Encephalopathy with a Reversible Splenial Lesion Associated with G5P[6]Rotavirus Infection von Komoto, Satoshi, Taniguchi, Koki, Matsuoka, Tsuyoshi, Ohfu, Masaharu, Akeda, Hideki, Matsuoka, Takashi, Yodoshi, Toshifumi, Sugai, Misaki, Hiyane, Masato

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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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Whole genomic analysis of a porcine-like human G5P[6] rotavirus strain isolated from a child with diarrhoea and encephalopathy in Japan von Komoto, Satoshi, Maeno, Yoshimasa, Tomita, Mayuko, Matsuoka, Tsuyoshi, Ohfu, Masaharu, Yodoshi, Toshifumi, Akeda, Hideki, Taniguchi, Koki

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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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Microchromosomal deletions involving SCNIA and adjacent genes in severe myoclonic epilepsy in infancy von WANG, Ji-Wen, KURAHASHI, Hirokazu, FUJII, Tatsuya, ITO, Masatoshi, OKUNO, Takehiko, SHIRASAKA, Yukiyoshi, NATSUME, Jun, HASEGAWA, Aki, KONAGAYA, Akihiko, KANEKO, Sunao, HIROSE, Shinichi, ISHII, Atsushi, KOJIMA, Toshio, OHFU, Masaharu, INOUE, Takahito, OGAWA, Atsushi, YASUMOTO, Sawa, OGUNI, Hirokazu, KURE, Shigeo

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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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Normal Development of the Pituitary Gland: Assessment with Three-dimensional MR Volumetry von Takano, Koichi, Utsunomiya, Hidetsuna, Ono, Hiroyuki, Ohfu, Masaharu, Okazaki, Masatoshi

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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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Favorable Seizure Outcome in Kabuki Make-up Syndrome Associated With Epilepsy von Ogawa, Atsushi, Yasumoto, Sawa, Tomoda, Yasuko, Ohfu, Masaharu, Mitsudome, Akihisa, Kuroki, Yoshikazu

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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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A Case of Encephalitis due to Mycoplasma pneurnoniae: Detection of Specific DNA from Cerebrospinal Fluid and Elevation of Interleukin-6 von INOUE, Shuichiro, OHFU, Masaharu, MOROOKA, Tatsuya, TSURU, Noboru, MITSUDOME, Akihisa, NARITA, Mitsuo

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