"Bitter Sweet": A Child Case of Erythritol-Induced Anaphylaxis von Shirao, Kenichiro, Inoue, Masami, Tokuda, Reiko, Nagao, Mizuho, Yamaguchi, Masao, Okahata, Hiroyasu, Fujisawa, Takao

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The novel IFNGR1 mutation 774del4 produces a truncated form of interferon-γ receptor 1 and has a dominant-negative effect on interferon-γ signal transduction von Okada, Satoshi, Ishikawa, Nobutsune, Shirao, Ken’ichiro, Kawaguchi, Hiroshi, Tsumura, Miyuki, Ohno, Yoshinori, Yasunaga, Shin’ichiro, Ohtsubo, Motoaki, Takihara, Yoshihiro, Kobayashi, Masao

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Significance of ACADM mutations identified through newborn screening of MCAD deficiency in Japan von Hara, Keiichi, Tajima, Go, Okada, Satoshi, Tsumura, Miyuki, Kagawa, Reiko, Shirao, Kenichiro, Ohno, Yoshinori, Yasunaga, Shin'ichiro, Ohtsubo, Motoaki, Hata, Ikue, Sakura, Nobuo, Shigematsu, Yosuke, Takihara, Yoshihiro, Kobayashi, Masao

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Wheeze Recognition Algorithm for Remote Medical Care Device in Children: Validation Study von Habukawa, Chizu, Ohgami, Naoto, Arai, Takahiko, Makata, Haruyuki, Tomikawa, Morimitsu, Fujino, Tokihiko, Manabe, Tetsuharu, Ogihara, Yoshihito, Ohtani, Kiyotaka, Shirao, Kenichiro, Sugai, Kazuko, Asai, Kei, Sato, Tetsuya, Murakami, Katsumi

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Polycomb-group complex 1 acts as an E3 ubiquitin ligase for Geminin to sustain hematopoietic stem cell activity von Ohtsubo, Motoaki, Yasunaga, Shin'ichiro, Ohno, Yoshinori, Tsumura, Miyuki, Okada, Satoshi, Ishikawa, Nobutsune, Shirao, Kenichiro, Kikuchi, Akira, Nishitani, Hideo, Kobayashi, Masao, Takihara, Yoshihiro

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Optimal step-down approach for pediatric asthma controlled by salmeterol/fluticasone: A randomized, controlled trial (OSCAR study) von Akashi, Kenichi, Mezawa, Hidetoshi, Tabata, Yuichi, Atsuta, Jun, Tokuda, Reiko, Kawada, Yasusuke, Kitamura, Tetsuro, Murasugi, Hiroko, Ito, Hiroaki, Tabata, Masahiko, Shirao, Kenichiro, Sato, Satoshi, Nishimura, Hideko, Fujiwara, Masako, Masuda, Kei, Arakawa, Hirokazu, Adachi, Yuichi, Yoshihara, Shigemi, Fujisawa, Takao, Katsunuma, Toshio

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Development of a New Enzymatic Diagnosis Method for Very-long-chain Acyl-CoA Dehydrogenase Deficiency by Detecting 2-Hexadecenoyl-CoA Production and its Application in Tandem Mass... von Tajima, Go, Sakura, Nobuo, Shirao, Kenichiro, Okada, Satoshi, Tsumura, Miyuki, Nishimura, Yutaka, Ono, Hiroaki, Hasegawa, Yuki, Hata, Ikue, Naito, Etsuo, Yamaguchi, Seiji, Shigematsu, Yosuke, Kobayashi, Masao

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The novel IFNGR1 mutation 774del4 produces a truncated form of interferon-  receptor 1 and has a dominant-negative effect on interferon-  signal transduction von Okada, S., Ishikawa, N., Shirao, K., Kawaguchi, H., Tsumura, M., Ohno, Y., Yasunaga, S., Ohtsubo, M., Takihara, Y., Kobayashi, M.

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Validation of the Wheeze Recognition Algorithm for Remote Medical Care Device in Children: Validation Study von Chizu, Habukawa, Ohgami, Naoto, Arai, Takahiko, Makata, Haruyuki, Tomikawa, Morimitsu, Fujino, Tokihiko, Manabe, Tetsuharu, Ogihara, Yoshihito, Ohtani, Kiyotaka, Shirao, Kenichiro, Sugai, Kazuko, Asai, Kei, Sato, Tetsuya, Murakami, Katsumi

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Molecular pathogenesis of a novel mutation, G108D, in short-chain acyl-CoA dehydrogenase identified in subjects with short-chain acyl-CoA dehydrogenase deficiency von Shirao, Kenichiro, Okada, Satoshi, Tajima, Go, Tsumura, Miyuki, Hara, Keiichi, Yasunaga, Shin'ichiro, Ohtsubo, Motoaki, Hata, Ikue, Sakura, Nobuo, Shigematsu, Yosuke, Takihara, Yoshihiro, Kobayashi, Masao

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Cardiac infiltration in early-onset sarcoidosis associated with a novel heterozygous mutation, G481D, in CARD15 von Okada, Satoshi, Konishi, Nakao, Tsumura, Miyuki, Shirao, Kenichiro, Yasunaga, Shin’ichiro, Sakai, Hidemasa, Nishikomori, Ryuta, Takihara, Yoshihiro, Kobayashi, Masao

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Novel Heterozygous Mutation 572insA in TACI Identified in a Patient with Selective IgA Deficiency von Okada, Satoshi, Kajiume, Teruyuki, Tsumura, Miyuki, Shirao, Kenichiro, Ohno, Yoshinori, Yasunaga, Shin'ichiro, Ohtsubo, Motoaki, Sira, Mostafa Mofamed, Kanegane, Hirokazu, Miyawaki, Toshio, Takihara, Yoshihiro, Kobayashi, Masao

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Association of Neurodevelopmental Abnormalities Is a Common Clinical Character in Japanese Patients with Severe Congenital Neutropenia Due to HAX1 Deficiency von Okada, Satoshi, Ishikawa, Nobutsune, Shirao, Kenichiro, Tsumura, Miyuki, Satoh, Takashi, Ohno, Yoshinori, Yasunaga, Shin'ichiro, Ohtsubo, Motoaki, Takihara, Yoshihiro, Kobayashi, Masao

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Surveys of pediatric asthma patients using Japanese Pediatric Asthma Control Program (JPAC) in Hiroshima area in 2008 and 2012 von Okahata, Hiroyasu, Okano, Rika, Ono, Atsushi, Kato, Yasuhiro, Kawaguchi, Hiroshi, Kitamura, Tetsuro, Sasaki, Nobutaka, Shirao, Kenichiro, Sugihara, Yuzo, Tsuji, Tetsuro, Fujitaka, Michiko, Yasui, Kozo, Ikeda, Masanori, Arita, Masahiko

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JP2869708B von SHIRAO KENICHIRO

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BOX TYPE NOISE FILTER von SHIRAO KENICHIRO

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"Bitter sweet": a child case of erythritol-induced anaphylaxis von Shirao, Kenichiro, Inoue, Masami, Tokuda, Reiko, Nagao, Mizuho, Yamaguchi, Masao, Okahata, Hiroyasu, Fujisawa, Takao

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Cardiac infiltration in early-onset sarcoidosis associated with a novel heterozygous mutation, G481D, in CARD15 von Okada, Satoshi, Konishi, Nakao, Tsumura, Miyuki, Shirao, Kenichiro, Yasunaga, Shin'ichiro, Sakai, Hidemasa, Nishikomori, Ryuta, Takihara, Yoshihiro, Kobayashi, Masao

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Progressive enrichment of arc magmas caused by the subduction of seamounts under Nishinoshima volcano, Izu–Bonin Arc, Japan von Sano, Takashi, Shirao, Motomaro, Tani, Kenichiro, Tsutsumi, Yukiyasu, Kiyokawa, Shoichi, Fujii, Toshitsugu

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