Two children with lymphocytic hypophysitis presenting with positive anti-rabphilin-3A antibody
Murai, An, Shinojima, Naoki, Ikuta, Genki, Ozono, Kazutaka, Ueda, Yutaka, Mabe, Hiroyo, Nakamura, Kenji, Iwata, Naoko, Fujisawa, Haruki, Nagamatsu, Fusa, Komatsu, Nagisa, Uekawa, Ken, Nishikawa, Shigeyuki, Nakamura, Kimitoshi, Mikami, Yoshiki, Suzuki, Atsushi, Sugimura, Yoshihisa, Mukasa, Akitake
Published in Endocrine Journal (01.01.2023)
Published in Endocrine Journal (01.01.2023)
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The Pharmacological Characteristics of Molecular-Based Inherited Salt-Losing Tubulopathies
Nozu, Kandai, Iijima, Kazumoto, Kanda, Kyoko, Nakanishi, Koichi, Yoshikawa, Norishige, Satomura, Kenichi, Kaito, Hiroshi, Hashimura, Yuya, Ninchoji, Takeshi, Komatsu, Hiroshi, Kamei, Koichi, Miyashita, Ritsuko, Kugo, Masaaki, Ohashi, Hiroshi, Yamazaki, Hajime, Mabe, Hiroyo, Otsubo, Asa, Igarashi, Takashi, Matsuo, Masafumi
Published in The journal of clinical endocrinology and metabolism (01.12.2010)
Published in The journal of clinical endocrinology and metabolism (01.12.2010)
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HRAS mutants identified in Costello syndrome patients can induce cellular senescence: possible implications for the pathogenesis of Costello syndrome
Niihori, Tetsuya, Aoki, Yoko, Okamoto, Nobuhiko, Kurosawa, Kenji, Ohashi, Hirofumi, Mizuno, Seiji, Kawame, Hiroshi, Inazawa, Johji, Ohura, Toshihiro, Arai, Hiroshi, Nabatame, Shin, Kikuchi, Kiyoshi, Kuroki, Yoshikazu, Miura, Masaru, Tanaka, Toju, Ohtake, Akira, Omori, Isaku, Ihara, Kenji, Mabe, Hiroyo, Watanabe, Kyoko, Niijima, Shinichi, Okano, Erika, Numabe, Hironao, Matsubara, Yoichi
Published in Journal of human genetics (01.10.2011)
Published in Journal of human genetics (01.10.2011)
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Systematic molecular analyses of SHOX in Japanese patients with idiopathic short stature and Leri-Weill dyschondrosteosis
Shima, Hirohito, Tanaka, Toshiaki, Kamimaki, Tsutomu, Dateki, Sumito, Muroya, Koji, Horikawa, Reiko, Kanno, Junko, Adachi, Masanori, Naiki, Yasuhiro, Tanaka, Hiroyuki, Mabe, Hiroyo, Yagasaki, Hideaki, Kure, Shigeo, Matsubara, Yoichi, Tajima, Toshihiro, Kashimada, Kenichi, Ishii, Tomohiro, Asakura, Yumi, Fujiwara, Ikuma, Soneda, Shun, Nagasaki, Keisuke, Hamajima, Takashi, Kanzaki, Susumu, Jinno, Tomoko, Ogata, Tsutomu, Fukami, Maki
Published in Journal of human genetics (01.07.2016)
Published in Journal of human genetics (01.07.2016)
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Journal Article
Epidemiology of anorexia nervosa in Japanese adolescents
Hotta, Mari, Horikawa, Reiko, Mabe, Hiroyo, Yokoyama, Shin, Sugiyama, Eiko, Yonekawa, Tadato, Nakazato, Masamitsu, Okamoto, Yuri, Ohara, Chisato, Ogawa, Yoshihiro
Published in BioPsychoSocial medicine (14.08.2015)
Published in BioPsychoSocial medicine (14.08.2015)
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NEUROD1‐deficient diabetes ( MODY6 ): Identification of the first cases in Japanese and the clinical features
Horikawa, Yukio, Enya, Mayumi, Mabe, Hiroyo, Fukushima, Kei, Takubo, Noriyuki, Ohashi, Masaaki, Ikeda, Fuki, Hashimoto, Ken‐ichi, Watada, Hirotaka, Takeda, Jun
Published in Pediatric diabetes (01.03.2018)
Published in Pediatric diabetes (01.03.2018)
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Journal Article
Learning and memorization impairment in childhood chronic fatigue syndrome manifesting as school phobia in Japan
Miike, Teruhisa, Tomoda, Akemi, Jhodoi, Takako, Iwatani, Noritaka, Mabe, Hiroyo
Published in Brain & development (Tokyo. 1979) (01.10.2004)
Published in Brain & development (Tokyo. 1979) (01.10.2004)
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Book Review
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Advantages and limitations of estrogen replacement therapy on hypogonadal survivors of childhood cancer
Nakamura, Miwa, Ohba, Takashi, Sasaki, Rumi, Saito, Fumitaka, Yamaguchi, Munekage, Motohara, Takeshi, Mabe, Hiroyo, Lu, Xi, Katabuchi, Hidetaka, Kondoh, Eiji
Published in International journal of clinical oncology (01.11.2023)
Published in International journal of clinical oncology (01.11.2023)
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Journal Article
NEUROD1‐deficient diabetes (MODY6): Identification of the first cases in Japanese and the clinical features
Horikawa, Yukio, Enya, Mayumi, Mabe, Hiroyo, Fukushima, Kei, Takubo, Noriyuki, Ohashi, Masaaki, Ikeda, Fuki, Hashimoto, Ken‐ichi, Watada, Hirotaka, Takeda, Jun
Published in Pediatric diabetes (01.03.2018)
Published in Pediatric diabetes (01.03.2018)
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Genotype–phenotype analysis, and assessment of the importance of the zinc-binding site in PHEX in Japanese patients with X-linked hypophosphatemic rickets using 3D structure modeling
Ishihara, Yasuki, Ohata, Yasuhisa, Takeyari, Shinji, Kitaoka, Taichi, Fujiwara, Makoto, Nakano, Yukako, Yamamoto, Kenichi, Yamada, Chieko, Yamamoto, Katsusuke, Michigami, Toshimi, Mabe, Hiroyo, Yamaguchi, Takeshi, Matsui, Katsuyuki, Tamada, Izumi, Namba, Noriyuki, Yamamoto, Akiko, Etoh, Junya, Kawaguchi, Azusa, Kosugi, Rieko, Ozono, Keiichi, Kubota, Takuo
Published in Bone (New York, N.Y.) (01.12.2021)
Published in Bone (New York, N.Y.) (01.12.2021)
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Long-term outcomes of multidisciplinary treatment combining surgery and stereotactic radiotherapy with Novalis for craniopharyngioma
Shinojima, Naoki, Yano, Shigetoshi, Uchida, Daichi, Mizukami, Naohisa, Mabe, Hiroyo, Kawashima, Junji, Igata, Motoyuki, Kondo, Tatsuya, Uetani, Hiroyuki, Yamamoto, Takahiro, Uekawa, Ken, Hide, Takuichiro, Mikami, Yoshiki, Hirai, Toshinori, Mukasa, Akitake
Published in Journal of clinical neuroscience (01.02.2024)
Published in Journal of clinical neuroscience (01.02.2024)
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MLL2 and KDM6A mutations in patients with Kabuki syndrome
Miyake, Noriko, Koshimizu, Eriko, Okamoto, Nobuhiko, Mizuno, Seiji, Ogata, Tsutomu, Nagai, Toshiro, Kosho, Tomoki, Ohashi, Hirofumi, Kato, Mitsuhiro, Sasaki, Goro, Mabe, Hiroyo, Watanabe, Yoriko, Yoshino, Makoto, Matsuishi, Toyojiro, Takanashi, Jun-Ichi, Shotelersuk, Vorasuk, Tekin, Mustafa, Ochi, Nobuhiko, Kubota, Masaya, Ito, Naoko, Ihara, Kenji, Hara, Toshiro, Tonoki, Hidefumi, Ohta, Tohru, Saito, Kayoko, Matsuo, Mari, Urano, Mari, Enokizono, Takashi, Sato, Astushi, Tanaka, Hiroyuki, Ogawa, Atsushi, Fujita, Takako, Hiraki, Yoko, Kitanaka, Sachiko, Matsubara, Yoichi, Makita, Toshio, Taguri, Masataka, Nakashima, Mitsuko, Tsurusaki, Yoshinori, Saitsu, Hirotomo, Yoshiura, Ko-Ichiro, Matsumoto, Naomichi, Niikawa, Norio
Published in American journal of medical genetics. Part A (01.09.2013)
Published in American journal of medical genetics. Part A (01.09.2013)
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Growth Hormone Injection Log Analysis with Electronic Injection Device for Qualifying Adherence to Low-Irritant Formulation and Exploring Influential Factors on Adherence
Takasawa, Kei, Mabe, Hiroyo, Nagamatsu, Fusa, Amano, Naoko, Miyakawa, Yuichi, Sutani, Akito, Kagawa, Reiko, Okada, Satoshi, Tanahashi, Yusuke, Suzuki, Shigeru, Hiroshima, Shota, Nagasaki, Keisuke, Dateki, Sumito, Takishima, Shigeru, Takahashi, Ikuko, Kashimada, Kenichi
Published in Patient preference and adherence (31.08.2023)
Published in Patient preference and adherence (31.08.2023)
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Glucoregulatory disorders in school refusal students
Iwatani, Noritaka, Miike, Teruhisa, Kai, Yumiko, Kodama, Mihoko, Mabe, Hiroyo, Tomoda, Akemi, Fukuda, Keiko, Jyodoi, Takako
Published in Clinical endocrinology (Oxford) (01.09.1997)
Published in Clinical endocrinology (Oxford) (01.09.1997)
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Present status of prophylactic thyroidectomy in pediatric multiple endocrine neoplasia 2: a nationwide survey in Japan 1997–2017
Matsushita, Rie, Nagasaki, Keisuke, Ayabe, Tadayuki, Miyoshi, Yoko, Kinjo, Saori, Haruna, Hidenori, Ihara, Kenji, Hasegawa, Tomonobu, Ida, Shinobu, Ozono, Keiichi, Minamitani, Kanshi
Published in Journal of Pediatric Endocrinology & Metabolism (26.06.2019)
Published in Journal of Pediatric Endocrinology & Metabolism (26.06.2019)
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Growth Hormone Advances Spermatogenesis in Premature Rats Treated with Gonadotropin-Releasing Hormone Agonist
OHYAMA, KENJI, IWATANI, NORITAKA, NAKAGOMI, YOSHIKO, OHTA, MASANORI, SHIMURA, YOSHIE, SANO, TOMOKI, SATO, KAZUMASA, OHNO, RIKA, MABE, HIROYO, ISHIKAWA, HIROMICHI, NAKAZAWA, SHINPEI
Published in Endocrine Journal (1999)
Published in Endocrine Journal (1999)
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Further delineation of the phenotype of chromosome 14q13 deletions: (positional) involvement of FOXG1 appears the main determinant of phenotype severity, with no evidence for a holoprosencephaly locus
Santen, Gijs W E, Sun, Yu, Gijsbers, Antoinet C J, Carré, Aurore, Holvoet, Maureen, Haeringen, Arie van, Lesnik Oberstein, Saskia A J, Tomoda, Akemi, Mabe, Hiroyo, Polak, Michel, Devriendt, Koenraad, Ruivenkamp, Claudia A L, Bijlsma, Emilia K
Published in Journal of medical genetics (01.06.2012)
Published in Journal of medical genetics (01.06.2012)
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A case of Turner syndrome complicated with brain infarction
Terasaki, Tadashi, Hashimoto, Yoichiro, Miyashita, Fumio, Kozaki, Yanosuke, Naganuma, Masaki, Uchino, Makoto, Mabe, Hiroyo
Published in Rinshō shinkeigaku (01.02.2002)
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Published in Rinshō shinkeigaku (01.02.2002)
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