Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Keinosuke Fujita"'
Publikováno v:
聖隷クリストファー大学看護学部紀要 = Bulletin School of Nursing Seirei Christopher University. 27:55-63
その他
Miscellaneous
本研究の目的は、学童期から青年期のターナー症候群（Turner syndrome、以下、TS とする）の女児と家族に対して、TS とTS 女児のQOL に関する意識の実態調査を実施
Miscellaneous
本研究の目的は、学童期から青年期のターナー症候群（Turner syndrome、以下、TS とする）の女児と家族に対して、TS とTS 女児のQOL に関する意識の実態調査を実施
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=jairo_______::28614f2ef1399b3e80a796a3622520b3
http://id.nii.ac.jp/1090/00001837/
http://id.nii.ac.jp/1090/00001837/
Publikováno v:
聖隷クリストファー大学看護学部紀要 = Bulletin School of Nursing Seirei Christopher University. 26:31-39
その他
Miscellaneous
【目的】小児看護における小児のQOL の概念の特徴を把握し、QOL の本質をとらえた尺度の開発への適応可能性について検討する。 【方法】 Rodgers（2000）の提唱す
Miscellaneous
【目的】小児看護における小児のQOL の概念の特徴を把握し、QOL の本質をとらえた尺度の開発への適応可能性について検討する。 【方法】 Rodgers（2000）の提唱す
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=jairo_______::da6bc253f4e4b187aae27d8c2238c7ac
http://id.nii.ac.jp/1090/00001715/
http://id.nii.ac.jp/1090/00001715/
Publikováno v:
聖隷クリストファー大学看護学部紀要 = Bulletin School of Nursing Seirei Christopher University. 26:41-49
その他
Miscellaneous
本研究は、ターナー症候群（Turner syndrome）の子ども（以下、TS 女児とする）の家族が抱く、子どもの成長・発達と成長・発達に関連した女児に対するQOL への思
Miscellaneous
本研究は、ターナー症候群（Turner syndrome）の子ども（以下、TS 女児とする）の家族が抱く、子どもの成長・発達と成長・発達に関連した女児に対するQOL への思
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=jairo_______::47cd7bdc722117b4b5c81bd21e0a47c4
http://id.nii.ac.jp/1090/00001716/
http://id.nii.ac.jp/1090/00001716/
Autor:
Akitoshi Tsuruhara, Takashi Hamazaki, Satsuki Nishigaki, Keinosuke Fujita, Toshiko Yoshida, Hiroshi Inada, Takuji Imamura, Haruo Shintaku
Publikováno v:
Endocrine journal. 64(5)
Turner syndrome results from the entire or partial loss of the second X chromosome, and is associated with a number of medical problems. Affected women require long-term medical follow-up. This study investigated the status of medical follow-up focus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5a5757fe0b0acbee8369614fbeb6a8c
https://pubmed.ncbi.nlm.nih.gov/28331102
https://pubmed.ncbi.nlm.nih.gov/28331102
Autor:
Tomonobu Hasegawa, Toshiaki Tanaka, Kunihiko Hanew, Keinosuke Fujita, Susumu Yokoya, Reiko Horikawa
Publikováno v:
Endocrine journal. 63(5)
In this study, the prevalence of obesity and complications of lifestyle-related diseases, such as diabetes mellitus, hypertension, dyslipidemia and liver dysfunction, as well as the relationship with karyotypes, were investigated in 492 patients with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1910c9a4af983cc1bc1ebaf27ff0761
https://pubmed.ncbi.nlm.nih.gov/26877182
https://pubmed.ncbi.nlm.nih.gov/26877182
Autor:
Masashi Shiomi, Kana Hosoki, Satsuki Nishigaki, Norio Niikawa, Shinji Saitoh, Keinosuke Fujita, Tohru Ohta
Publikováno v:
Pediatrics International. 54:e22-e25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f05af3a2d7224612de99e9f8cba4ac1c
https://doi.org/10.1111/j.1442-200x.2011.03550.x
https://doi.org/10.1111/j.1442-200x.2011.03550.x
Autor:
Kenji Ohyama, Toru Yorifuji, Hitoshi Kohno, Katsuhiko Tachibana, Hiroaki Takahashi, Susumu Kanzaki, Kenji Fujieda, Reiko Horikawa, Hiroyuki Tanaka, Susumu Yokoya, Toshiaki Tanaka, Keiichi Ozono, Yutaka Igarashi, Yoshikazu Nishi, Hisao Osada, Tomonobu Hasegawa, Kazumichi Onigata, Masamichi Ogawa, Keinosuke Fujita, Toshihiro Tajima, Yoshiki Seino
Publikováno v:
Clinical Pediatric Endocrinology
Background: Patients with Turner syndrome (TS) are prone to having metabolic abnormalities, such as obesity, dyslipidemia, hypertension, hyperinsulinemia and type 2 diabetes mellitus, resulting in increased risks of developing atherosclerotic disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc2f9e63a5534f04eca3dbb35f89bb36
https://doi.org/10.1297/cpe.21.29
https://doi.org/10.1297/cpe.21.29
Autor:
Yukihiro Hasegawa, Takakuni Tanizawa, Susumu Yokoya, Akira Teramoto, Akira Shimatsu, Toshiaki Tanaka, Yoshikazu Nishi, Kunihiko Hanew, Reiko Horikawa, Toshiro Nagai, Katsuhiko Tachibana, Keinosuke Fujita, Kenji Fujieda, Hiroaki Tanaka
Publikováno v:
Clinical Pediatric Endocrinology
Growth hormone (GH) therapy was approved in 1999 for only GH-deficient Turner syndrome (TS) in Japan. It was subsequently approved for all cases of TS regardless of GH secretory status since 1999. The dose of GH is 1.0 u (0.35 mg)/kg/wk at present, b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66d3a4064bada02c992b52f72af59b77
https://doi.org/10.1297/cpe.19.63
https://doi.org/10.1297/cpe.19.63
Autor:
Tsutomu Ogata, Koji Muroya, Keinosuke Fujita, Mitsuo Itakura, Maki Fukami, Takahiro Mochizuki, Manami Iso
Publikováno v:
Endocrine Journal. 57:171-174
We report on a Japanese girl with HDR (hypoparathyroidism, sensorineural deafness, and renal dysplasia) syndrome who developed diabetes mellitus (DM) at three years of age (blood glucose 713 mg/dL, HbA(1c) 8.0%) in the absence of anti-glutamic acid d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::959abd4f58b39848ebc15c9da317a1d1
https://doi.org/10.1507/endocrj.k09e-313
https://doi.org/10.1507/endocrj.k09e-313
Autor:
Masamichi Ogawa, Toshihiro Tajima, Yoshikazu Nishi, Yoshiki Seino, Hisao Osada, Kenji Ohyama, Tomonobu Hasegawa, Reiko Horikawa, Tohru Yorifuji, Keinosuke Fujita, Keiichi Ozono, Katsuhiko Tachibana, Susumu Kanzaki, Hiroaki Takahashi, Hiroyuki Tanaka, Hitoshi Kohno, Kazumichi Onigata, Susumu Yokoya, Toshiaki Tanaka, Yutaka Igarashi
Publikováno v:
Clinical Pediatric Endocrinology
The Growject® database on human GH treatment in Turner syndrome was analyzed in the Turner Syndrome Research Collaboration, and the relationships of the frequencies of spontaneous breast development and spontaneous menarche with karyotype and GH tre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fe61c900c919bc4ef7906e5e7fc528d
https://pubmed.ncbi.nlm.nih.gov/26568657
https://pubmed.ncbi.nlm.nih.gov/26568657