Earthquake disaster footage and its effects on children: Request to the media to help protect children von Osawa, Makiko

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CUX2 deficiency causes facilitation of excitatory synaptic transmission onto hippocampus and increased seizure susceptibility to kainate von 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

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Mouse with Nav1.1 haploinsufficiency, a model for Dravet syndrome, exhibits lowered sociability and learning impairment von Ito, Susumu, Ogiwara, Ikuo, Yamada, Kazuyuki, Miyamoto, Hiroyuki, Hensch, Takao K., Osawa, Makiko, Yamakawa, Kazuhiro

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Epilepsy associated with Graves’ disease: Report of two cases von Nagaki, Shigeru, Osawa, Makiko, Nagata, Satoru

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Outcome of vagus nerve stimulation for drug‐resistant epilepsy: the first three years of a prospective Japanese registry von Kawai, Kensuke, Tanaka, Tatsuya, Baba, Hiroshi, Bunker, Mark, Ikeda, Akio, Inoue, Yushi, Kameyama, Shigeki, Kaneko, Sunao, Kato, Amami, Nozawa, Taneyoshi, Maruoka, Eiji, Osawa, Makiko, Otsuki, Taisuke, Tsuji, Sadatoshi, Watanabe, Eiju, Yamamoto, Takamichi

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A case of Turner’s syndrome with Graves’ disease and primary hyperparathyroidism von Nagaki, Shigeru, Tachikawa, Emiko, Kodama, Hitomi, Obara, Takao, Osawa, Makiko, Nagata, Satoru

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Turner syndrome with idiopathic thrombocytopenic purpura in childhood von Nagaki, Shigeru, Miwa, Kumiko, Tsunematsu, Yukiko, Osawa, Makiko, Nagata, Satoru

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Deep-intronic variant of fukutin is the most prevalent point mutation of Fukuyama congenital muscular dystrophy in Japan von Kobayashi, Kazuhiro, Kato, Reiko, Kondo-Iida, Eri, Taniguchi-Ikeda, Mariko, Osawa, Makiko, Saito, Kayoko, Toda, Tatsushi

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Ketogenic diet therapy can improve ACTH-resistant West syndrome in Japan von Hirano, Yoshiko, Oguni, Hirokazu, Shiota, Mutuko, Nishikawa, Aiko, Osawa, Makiko

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Antisense PMO found in dystrophic dog model was effective in cells from exon 7-deleted DMD patient von Saito, Takashi, Nakamura, Akinori, Aoki, Yoshitsugu, Yokota, Toshifumi, Okada, Takashi, Osawa, Makiko, Takeda, Shin'ichi

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Retrospective multiinstitutional study of the prevalence of early death in Dravet syndrome von Sakauchi, Masako, Oguni, Hirokazu, Kato, Ikuko, Osawa, Makiko, Hirose, Shinichi, Kaneko, Sunao, Takahashi, Yukitoshi, Takayama, Rumiko, Fujiwara, Tateki

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Yukio Fukuyama, MD (1928–2014) von Osawa, Makiko, MD, PhD

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Mortality in Dravet syndrome: Search for risk factors in Japanese patients von Sakauchi, Masako, Oguni, Hirokazu, Kato, Ikuko, Osawa, Makiko, Hirose, Shinichi, Kaneko, Sunao, Takahashi, Yukitoshi, Takayama, Rumiko, Fujiwara, Tateki

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Arginase deficiency with parotid gland swelling and hyperamylasemia: A case report von Kuyama, Noboru, Nagaki, Shigeru, Miyamoto, Akie, Etou, Kaoru, Maruyama, Hiroshi, Osawa, Makiko

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A short form of gross motor function measure for Fukuyama congenital muscular dystrophy von Sato, Takatoshi, Adachi, Michiru, Matsuo, Aya, Zushi, Masaya, Goto, Keisuke, Hirose, Megumi, Ishiguro, Kumiko, Shichiji, Minobu, Murakami, Terumi, Ikai, Tetsuo, Osawa, Makiko, Kondo, Izumi, Nagata, Satoru, Ishigaki, Keiko

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Study of epileptic drop attacks in symptomatic epilepsy of early childhood – Differences from those in myoclonic-astatic epilepsy von Itoh, Yasushi, Oguni, Hirokazu, Hirano, Yoshiko, Osawa, Makiko

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CDKL5 alterations lead to early epileptic encephalopathy in both genders von Liang, Jao‐Shwann, Shimojima, Keiko, Takayama, Rumiko, Natsume, Jun, Shichiji, Minobu, Hirasawa, Kyoko, Imai, Kaoru, Okanishi, Tohru, Mizuno, Seiji, Okumura, Akihisa, Sugawara, Midori, Ito, Tomoshiro, Ikeda, Hiroko, Takahashi, Yukitoshi, Oguni, Hirokazu, Imai, Katsumi, Osawa, Makiko, Yamamoto, Toshiyuki

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The gross motor function measure is valid for Fukuyama congenital muscular dystrophy von Sato, Takatoshi, Adachi, Michiru, Nakamura, Kaho, Zushi, Masaya, Goto, Keisuke, Murakami, Terumi, Ishiguro, Kumiko, Shichiji, Minobu, Saito, Kayoko, Ukai, Tetsuo, Osawa, Makiko, Kondo, Izumi, Nagata, Satoru, Ishigaki, Keiko

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Renal dysfunction is rare in Fukuyama congenital muscular dystrophy von Ishigaki, Keiko, Kato, Ikuko, Murakami, Terumi, Sato, Takatoshi, Shichiji, Minobu, Ishiguro, Kumiko, Ishizuka, Kiyonobu, Funatsuka, Makoto, Saito, Kayoko, Osawa, Makiko, Nagata, Satoru

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Characteristic findings of skeletal muscle MRI in caveolinopathies von Ishiguro, Kumiko, Nakayama, Takahiro, Yoshioka, Masaru, Murakami, Terumi, Kajino, Sachiko, Shichiji, Minobu, Sato, Takatoshi, Hino-Fukuyo, Naomi, Kuru, Satoshi, Osawa, Makiko, Nagata, Satoru, Okubo, Mariko, Murakami, Nobuyuki, Hayashi, Yukiko K, Nishino, Ichizo, Ishigaki, Keiko

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