Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Yukako Yamamoto"'
Autor:
Yukako Yamamoto, Takeshi Togawa, Osamu Sekine, Yuki Ozamoto, Junko Fuse, Choka Azuma, Jun Ito-Kobayashi, Yasumitsu Oe, Akeo Hagiwara, Masaki Kobayashi, Tadahiro Kitamura, Masanori Iwanishi, Akira Shimatsu, Atsunori Kashiwagi
Publikováno v:
Endocrine Journal, Vol 70, Iss 12, Pp 1141-1157 (2023)
To determine the normalization of postprandial blood glucose (PG) and triglyceride (TG) excursions in 30 morbidly obese patients with or without diabetes mellitus (DM) 1-year after they underwent a laparoscopic sleeve gastrectomy (LSG) vs. their pre-
Externí odkaz:
https://doaj.org/article/4f01e7c907f94ea690a13c97ccf31a53
Autor:
Masaki Kobayashi, Nobuhiro Maruyama, Yukako Yamamoto, Takeshi Togawa, Takanori Ida, Morikatsu Yoshida, Mikiya Miyazato, Masahisa Kitada, Yoshitaka Hayashi, Atsunori Kashiwagi, Tadahiro Kitamura
Publikováno v:
Journal of Diabetes Investigation, Vol 14, Iss 5, Pp 648-658 (2023)
Abstract Aims/Introduction Glucagon, a peptide hormone produced from proglucagon, is involved in the pathophysiology of diabetes. Plasma glucagon levels are currently measured by sandwich enzyme‐linked immunosorbent assay (ELISA), but the currently
Externí odkaz:
https://doaj.org/article/eb79ea82f73f49fda8578206521f0f74
Autor:
Yukako, Yamamoto, Yuki, Ozamoto, Masaki, Kobayashi, Yuji, Tezuka, Choka, Azuma, Osamu, Sekine, Jun, Ito-Kobayashi, Miki, Washiyama, Yasumitsu, Oe, Masanori, Iwanishi, Takeshi, Togawa, Akeo, Hagiwara, Tadahiro, Kitamura, Akira, Shimatsu, Atsunori, Kashiwagi
Publikováno v:
Endocrine Journal. 69:689-703
A new meal tolerance test (MTT) using a 75 g glucose- and high fat-containing meal was applied to classify glucose intolerance in morbidly obese patients. According to the MTT data, the concordance rate of diagnosis was 82.5% compared to the 75 g ora
Autor:
Jun Ito-Kobayashi, Miki Washiyama, Yuji Tezuka, Shingo Kikugawa, Yukako Yamamoto, Masanori Iwanishi, Toru Kusakabe, Choka Azuma
Publikováno v:
Internal Medicine
Mysterin, which was recently shown to play an important role in maintaining cellular fat storage, has been identified to be the susceptibility gene for moyamoya disease (MMD). We encountered some female Japanese patients with partial lipodystrophy an
Autor:
Yuji Tezuka, Jun Ito-Kobayashi, Ikuhisa Nakanishi, Choka Azuma, Miyuki Furuta, Miki Washiyama, Yukako Yamamoto, Osamu Sekine, Akiko Hirano, Hanada Yukako, Ariga Misaki, Atsunori Kashiwagi, Masao Kanamori, Akira Shimatsu, Masanori Iwanishi
Publikováno v:
Diabetes Therapy
Introduction Various types of skin lesions with pruritus have been reported in participants of Asian clinical trials on sodium-glucose cotransporter-2 (SGLT2) inhibitors. The aim of this study was to determine whether the diuretic effect of a SGLT2 i
Autor:
Jun Ito-Kobayashi, Choka Azuma, Yuji Tezuka, Mayumi Morimoto, Masanori Iwanishi, Toru Kusakabe, Ken Ebihara, Yukako Yamamoto, Miki Washiyama
Publikováno v:
Diabetes Research and Clinical Practice. 152:79-87
Aims The present report aimed to clarify the clinical characteristics in a girl at the age of 12 and her mother with partial lipodystrophy and Type A insulin resistance syndrome. Methods We examined fat distribution in the patients using dual-energy
[Biomarkers of Leukemia ~Description of the Practical Use and Operation in the Clinical Laboratory~]
Autor:
Yoko, Kajiura, Yukako, Yamamoto, Kanae, Okada, Hikaru, Hattori, Hiroyuki, Matsumoto, Mayuko, Kishimoto, Tadashi, Matsushita
Publikováno v:
Rinsho byori. The Japanese journal of clinical pathology. 65(1)
Genetic testing of hematological malignancy is-.indispensable to categorize and diagnose leukemia. The quantitation of fusion gene mRNA built up by chromosomal translocation including BCR-ABL1 (major, minor), RUNX1-RUNX1T1, and PML-RARA and detection
Autor:
Naohiro Kanayama, Isamu Sugiura, Kazuo Kagami, Yuka Nomura, Takayuki Iwaki, Junki Takamatsu, Tetsuhito Kojima, Hidehiko Saito, Takayuki Nakayama, Takao Kobayashi, Tadashi Mastushita, Yukako Yamamoto
Publikováno v:
Seminars in Thrombosis and Hemostasis. 27:155-160
The molecular basis for the hereditary type I protein S (PS) deficiency was investigated. DNA sequence analysis of 12 patients with PS deficiency in Japan identified four point mutations and three of them were novel. Nonsense mutations found in two u
Publikováno v:
Journal of Diabetes Investigation. 2023 Supplement 1, Vol. 14 Issue 1, p5-221. 217p.
Autor:
Kobayashi, Masaki1 (AUTHOR), Maruyama, Nobuhiro2 (AUTHOR), Yamamoto, Yukako3 (AUTHOR), Togawa, Takeshi4 (AUTHOR), Ida, Takanori5 (AUTHOR), Yoshida, Morikatsu6 (AUTHOR), Miyazato, Mikiya6 (AUTHOR), Kitada, Masahisa7 (AUTHOR), Hayashi, Yoshitaka8 (AUTHOR), Kashiwagi, Atsunori3 (AUTHOR), Kitamura, Tadahiro1 (AUTHOR) kitamura@gunma-u.ac.jp
Publikováno v:
Journal of Diabetes Investigation. May2023, Vol. 14 Issue 5, p648-658. 11p.