Zobrazeno 1 - 10
of 1 523
pro vyhledávání: '"R. Shima"'
Autor:
Atsushi Tanaka, Michio Shimabukuro, Noritaka Machii, Hiroki Teragawa, Yosuke Okada, Kosuke R. Shima, Toshinari Takamura, Isao Taguchi, Itaru Hisauchi, Shigeru Toyoda, Yasushi Matsuzawa, Hirofumi Tomiyama, Minako Yamaoka‐Tojo, Shinichiro Ueda, Yukihito Higashi, Koichi Node
Publikováno v:
Journal of Diabetes Investigation, Vol 11, Iss 6, Pp 1551-1563 (2020)
Abstract Aims/Introduction Recent clinical trials on sodium–glucose cotransporter 2 inhibitors showed improved outcomes in patients with type 2 diabetes at a high risk of cardiovascular events. However, the underlying effects on endothelial functio
Externí odkaz:
https://doaj.org/article/b4a23468947b43a3af27927cc69d5925
Autor:
Atsushi Tanaka, Michio Shimabukuro, Yosuke Okada, Isao Taguchi, Minako Yamaoka-Tojo, Hirofumi Tomiyama, Hiroki Teragawa, Seigo Sugiyama, Hisako Yoshida, Yasunori Sato, Atsushi Kawaguchi, Yumi Ikehara, Noritaka Machii, Tatsuya Maruhashi, Kosuke R. Shima, Toshinari Takamura, Yasushi Matsuzawa, Kazuo Kimura, Masashi Sakuma, Jun-ichi Oyama, Teruo Inoue, Yukihito Higashi, Shinichiro Ueda, Koichi Node, On Behalf of the EMBLEM Trial Investigators
Publikováno v:
Cardiovascular Diabetology, Vol 16, Iss 1, Pp 1-12 (2017)
Abstract Background Type 2 diabetes mellitus (T2DM) is characterized by systemic metabolic abnormalities and the development of micro- and macrovascular complications, resulting in a shortened life expectancy. A recent cardiovascular (CV) safety tria
Externí odkaz:
https://doaj.org/article/03047384b5c34598bbc3090a5fe2a771
Autor:
Yakov Roizin, Yossi Rosenwaks, Zoe Mutsafi, Klimentiy Shimanovich, Victor Kairys, R. Shima-Edelstein
Publikováno v:
IEEE Transactions on Electron Devices. 68:5695-5700
This article reports on the high-temperature (HT) operation (25 °C–400 °C) and temperature sensing mechanism of a depletion-mode AlGaN/GaN metal–insulator–semiconductor (MIS) high-electron-mobility transistor (depletion mode (D-mode) AlGaN/Ga
Autor:
Yasushi Matsuzawa, Shigeru Toyoda, Shinichiro Ueda, Noritaka Machii, Kosuke R. Shima, Isao Taguchi, Hirofumi Tomiyama, Koichi Node, Hiroki Teragawa, Itaru Hisauchi, Toshinari Takamura, Minako Yamaoka-Tojo, Atsushi Tanaka, Yosuke Okada, Michio Shimabukuro, Yukihito Higashi
Publikováno v:
Journal of Diabetes Investigation
Journal of Diabetes Investigation, Vol 11, Iss 6, Pp 1551-1563 (2020)
Journal of Diabetes Investigation, Vol 11, Iss 6, Pp 1551-1563 (2020)
Aims/Introduction Recent clinical trials on sodium–glucose cotransporter 2 inhibitors showed improved outcomes in patients with type 2 diabetes at a high risk of cardiovascular events. However, the underlying effects on endothelial function remain
Akademický článek
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Publikováno v:
IOP Conference Series: Earth and Environmental Science. 1079:012024
This paper describes the mechanism of extraordinary transient stress that occurs during start-up of a Francis turbine by investigating the detailed analysis with measured stress of prototype runner and transient response calculation. According to the
Autor:
Toshio Kahara, Hitomi Wakakuri, Juri Takatsuji, Iori Motoo, Kosuke R. Shima, Kazuhide Ishikura, Rika Usuda, Yatsugi Noda
Publikováno v:
Case Reports in Endocrinology, Vol 2012 (2012)
A 71-year-old man with diabetes mellitus visited our hospital with complaints of anorexia and weight loss (12 kg/3 months). He had megaloblastic anemia, cobalamin level was low, and autoantibody to intrinsic factor was positive. He was treated with i
Externí odkaz:
https://doaj.org/article/9a9a82544f414f03ad957a89047e9fba
Autor:
Rika Usuda, Toshinari Takamura, Kosuke R. Shima, Takeshi Futatani, Hiroshi Akahori, Tohru Yorifuji, Shuichi Kaneko
Publikováno v:
Endocrine Journal. 65:1055-1059
Gain-of-function ATP-binding cassette subfamily C member 8 (ABCC8) mutations are known to cause neonatal diabetes mellitus and maturity-onset diabetes in the young. However, the intrafamilial heterogeneous nature of diabetes caused by the ABCC8 mutat
Publikováno v:
Human Genome Variation, Vol 6, Iss 1, Pp 1-3 (2019)
Human Genome Variation
Human Genome Variation
X-linked hypophosphatemic rickets (XLH) is the most common form of hereditary rickets. Here, we present a case of XLH associated with a novel mutation in a phosphate-regulating gene with homologies to endopeptidases on the X chromosome (PHEX). PCR-di
Akademický článek
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