Wheeze Recognition Algorithm for Remote Medical Care Device in Children: Validation Study
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
Published in JMIR pediatrics and parenting (17.06.2021)
Published in JMIR pediatrics and parenting (17.06.2021)
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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
Okada, Satoshi, Ishikawa, Nobutsune, Shirao, Ken’ichiro, Kawaguchi, Hiroshi, Tsumura, Miyuki, Ohno, Yoshinori, Yasunaga, Shin’ichiro, Ohtsubo, Motoaki, Takihara, Yoshihiro, Kobayashi, Masao
Published in Journal of medical genetics (01.08.2007)
Published in Journal of medical genetics (01.08.2007)
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Significance of ACADM mutations identified through newborn screening of MCAD deficiency in Japan
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
Published in Molecular genetics and metabolism (01.05.2016)
Published in Molecular genetics and metabolism (01.05.2016)
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Polycomb-group complex 1 acts as an E3 ubiquitin ligase for Geminin to sustain hematopoietic stem cell activity
Ohtsubo, Motoaki, Yasunaga, Shin'ichiro, Ohno, Yoshinori, Tsumura, Miyuki, Okada, Satoshi, Ishikawa, Nobutsune, Shirao, Kenichiro, Kikuchi, Akira, Nishitani, Hideo, Kobayashi, Masao, Takihara, Yoshihiro
Published in Proceedings of the National Academy of Sciences - PNAS (29.07.2008)
Published in Proceedings of the National Academy of Sciences - PNAS (29.07.2008)
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Optimal step-down approach for pediatric asthma controlled by salmeterol/fluticasone: A randomized, controlled trial (OSCAR study)
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
Published in Allergology International (01.07.2016)
Published in Allergology International (01.07.2016)
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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 Spectrometry-based Selective Screening and Newborn Screening in Japan
TAJIMA, Go, SAKURA, Nobuo, YAMAGUCHI, Seiji, SHIGEMATSU, Yosuke, KOBAYASHI, Masao, SHIRAO, Kenichiro, OKADA, Satoshi, TSUMURA, Miyuki, NISHIMURA, Yutaka, ONO, Hiroaki, HASEGAWA, Yuki, HATA, Ikue, NAITO, Etsuo
Published in Pediatric research (01.12.2008)
Published in Pediatric research (01.12.2008)
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Validation of the Wheeze Recognition Algorithm for Remote Medical Care Device in Children: Validation Study
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
Published in JMIR pediatrics and parenting (16.04.2021)
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Published in JMIR pediatrics and parenting (16.04.2021)
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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
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
Published in Human genetics (01.06.2010)
Published in Human genetics (01.06.2010)
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Cardiac infiltration in early-onset sarcoidosis associated with a novel heterozygous mutation, G481D, in CARD15
Okada, Satoshi, Konishi, Nakao, Tsumura, Miyuki, Shirao, Kenichiro, Yasunaga, Shin’ichiro, Sakai, Hidemasa, Nishikomori, Ryuta, Takihara, Yoshihiro, Kobayashi, Masao
Published in Rheumatology (Oxford, England) (01.06.2009)
Published in Rheumatology (Oxford, England) (01.06.2009)
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Novel Heterozygous Mutation 572insA in TACI Identified in a Patient with Selective IgA Deficiency
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
Published in Blood (16.11.2008)
Published in Blood (16.11.2008)
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Association of Neurodevelopmental Abnormalities Is a Common Clinical Character in Japanese Patients with Severe Congenital Neutropenia Due to HAX1 Deficiency
Okada, Satoshi, Ishikawa, Nobutsune, Shirao, Kenichiro, Tsumura, Miyuki, Satoh, Takashi, Ohno, Yoshinori, Yasunaga, Shin'ichiro, Ohtsubo, Motoaki, Takihara, Yoshihiro, Kobayashi, Masao
Published in Blood (16.11.2007)
Published in Blood (16.11.2007)
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"Bitter sweet": a child case of erythritol-induced anaphylaxis
Shirao, Kenichiro, Inoue, Masami, Tokuda, Reiko, Nagao, Mizuho, Yamaguchi, Masao, Okahata, Hiroyasu, Fujisawa, Takao
Published in Allergology international : official journal of the Japanese Society of Allergology (01.06.2013)
Published in Allergology international : official journal of the Japanese Society of Allergology (01.06.2013)
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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
Okada, S., Ishikawa, N., Shirao, K., Kawaguchi, H., Tsumura, M., Ohno, Y., Yasunaga, S., Ohtsubo, M., Takihara, Y., Kobayashi, M.
Published in Journal of medical genetics (16.03.2007)
Published in Journal of medical genetics (16.03.2007)
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Journal Article
Cardiac infiltration in early-onset sarcoidosis associated with a novel heterozygous mutation, G481D, in CARD15
Okada, Satoshi, Konishi, Nakao, Tsumura, Miyuki, Shirao, Kenichiro, Yasunaga, Shin'ichiro, Sakai, Hidemasa, Nishikomori, Ryuta, Takihara, Yoshihiro, Kobayashi, Masao
Published in Rheumatology (Oxford, England) (01.06.2009)
Published in Rheumatology (Oxford, England) (01.06.2009)
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