Zobrazeno 1 - 10
of 105
pro vyhledávání: '"Goro Sasaki"'
Autor:
Kyohei Furusawa, Rumi Hachiya, Hironori Shibata, Noboru Uchida, Goro Sasaki, Hiroyuki Fukushima, Tomohiro Ishii, Tomonobu Hasegawa
Publikováno v:
Clinical Pediatric Endocrinology; Jan2024, Vol. 33 Issue 1, p35-38, 4p
Autor:
Yuki Abe, Tatsuhiko Urakami, Junichi Suzuki, Satoshi Morita, Mariko Araki, Michiyo Mizota, Goro Sasaki, Jun Mori, Toshi Tatematsu, Yusuke Mine, Kei Yoshida, Toru Kikuchi
Publikováno v:
Endocrine Journal.
Autor:
Kenichiro Hata, Yoko Tanaka, Kazuhiro Ogata, Shuji Takada, Keisuke Nagasaki, Goro Sasaki, Masaaki Shiina, Tsutomu Ogata, Miho Terao, Mami Miyado, Maki Fukami, Hirotomo Saitsu, Youhei Masunaga, Yoichi Matsubara, Kazuhiko Nakabayashi
Publikováno v:
Journal of the American Society of Nephrology. 30:877-889
Background The stimulatory G-protein α -subunit encoded by GNAS exons 1–13 ( GNAS -Gs α ) mediates signal transduction of multiple G protein–coupled receptors, including arginine vasopressin receptor 2 (AVPR2). Various germline-derived loss-of-
Autor:
Keiko Homma, Seiji Sato, Naoaki Hori, Tomohiro Ishii, Tomonobu Hasegawa, Naoko Amano, Goro Sasaki
Publikováno v:
Endocrine Journal. 66:837-842
Steroid 5α-reductase type 2 deficiency (5αRD2) is a congenital disorder of sex development caused by impairment of conversion from testosterone (T) to 5α-dihydrotestosterone (DHT). DHT deficiency leads to various degrees of undervirilized external
Autor:
Satoshi Narumi, Keiko Homma, Tomonobu Hasegawa, Kazuhide Imai, Mie Hayashi, Tomohiro Ishii, Naoko Amano, Toshirou Nakamura, Masaki Takagi, Rumi Hachiya, Goro Sasaki
Publikováno v:
European Journal of Endocrinology. 177:187-194
Context Most patients with pediatric-onset primary adrenal insufficiency (PAI), such as 21-hydroxylase deficiency, can be diagnosed by measuring the urine or serum levels of steroid metabolites. However, the etiology is often difficult to determine i
Autor:
Tatsuhiko Urakami, Nobuo Matsuura, Kenji Ihara, Tsutomu Ogata, Kisho Kobayashi, Adolescent Diabetes, Shun Soneda, Naoto Shimura, T. Mori, S. Teno, Koji Takemoto, Tokuo Mukai, Kanshi Minamitani, Tomoyuki Kawamura, Toshikazu Takahashi, Toru Kikuchi, Shin Amemiya, Nobuyuki Kikuchi, Keiichi Hanaki, Shigetaka Sugihara, Tadayuki Ayabe, Susumu Kanzaki, Yasuhiro Igarashi, Noriyuki Takubo, Reiko Horikawa, Zenro Kizaki, Takahiro Mochizuki, Rika Kizu, Ryuzo Takaya, Goro Sasaki, Kitaro Kosaka, T. Fujisawa, Ichiro Yokota, Seiichi Matsuo, Yoshihito Kasahara, Kohji Tsubouchi, Maki Fukami, Akemi Koike, Hiroshi Mochizuki, Aki Nishii
Publikováno v:
Diabetic Medicine. 33:1717-1722
Aims The aim of this study was to clarify the significance of previously reported susceptibility variants in the development of autoimmune Type 1 diabetes in non-white children. Tested variants included rs2290400, which has been linked to Type 1 diab
Autor:
Haruo Mizuno, Tatsuhiko Urakami, Shin Amemiya, Kazuteru Kitsuda, Motohide Goto, Toru Kikuchi, Yuki Abe, Shigetaka Sugihara, Kohji Tsubouchi, Yukiyo Yamamoto, Goro Sasaki
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 32(1)
BackgroundTreatment for type 1 diabetes mellitus (T1DM) has greatly changed by the general use of insulin analogs and continuous subcutaneous insulin infusion (CSII). To investigate whether these advances have been translated into continued improveme
Autor:
Satoshi Narumi, Nobutake Matsuo, Makoto Anzo, Shinya Tamai, Naoaki Hori, Tsutomu Kamimaki, Tomohiro Ishii, Tsutomu Ogata, Mikako Inokuchi, Hironori Shibata, Seiji Sato, Naoko Amano, Goro Sasaki, Tomonobu Hasegawa
Publikováno v:
Hormone Research in Paediatrics. 84:305-310
Background/Aim: To evaluate the accuracy of the human chorionic gonadotropin (hCG) stimulation test in children with micropenis in predicting later Leydig cell function. Methods: We conducted a retrospective investigation of testosterone response to
Autor:
Hidefumi Tonoki, Mitsuhiro Kato, Atsushi Ogawa, Jun-ichi Takanashi, Toshiro Nagai, Takashi Enokizono, Nobuhiko Okamoto, Sachiko Kitanaka, Naoko Ito, Eriko Koshimizu, Mustafa Tekin, Naomichi Matsumoto, Takako Fujita, Kayoko Saito, Nobuhiko Ochi, Toshio Makita, Astushi Sato, Ko Ichiro Yoshiura, Hiroyuki Tanaka, Masataka Taguri, Makoto Yoshino, Yoko Hiraki, Yoichi Matsubara, Hirotomo Saitsu, Tomoki Kosho, Mari Urano, Seiji Mizuno, Norio Niikawa, Kenji Ihara, Hirofumi Ohashi, Yoshinori Tsurusaki, Mitsuko Nakashima, Noriko Miyake, Yoriko Watanabe, Mari Matsuo, Toshiro Hara, Hiroyo Mabe, Toyojiro Matsuishi, Vorasuk Shotelersuk, Masaya Kubota, Goro Sasaki, Tsutomu Ogata, Tohru Ohta
Publikováno v:
American Journal of Medical Genetics Part A. 161:2234-2243
Kabuki syndrome is a congenital anomaly syndrome characterized by developmental delay, intellectual disability, specific facial features including long palpebral fissures and ectropion of the lateral third of the lower eyelids, prominent digit pads,
Autor:
Goro Sasaki
Publikováno v:
Material Cycles and Waste Management Research. 28:327-328