Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Miki Washiyama"'
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:
Shinichi Shiona, Shoichiro Kanda, Shuichi Ito, Ryoko Harada, Satoshi Tazoe, Motoshi Hattori, Shinichiro Ohara, Shogo Minamikawa, Naoya Morisada, Kenji Ishikura, Tomohiko Yamamura, Yukiko Mori, Daisuke Aotani, Mayumi Enseki, Hiroyo Kourakata, Katsuaki Kasahara, Miki Washiyama, China Nagano, Kazumoto Iijima, Kandai Nozu, Nana Sakakibara, Yoshinori Araki, Koichi Kamei, Takeshi Yamada, Kenichiro Miura, Ryojiro Tanaka, Akane Seo, Chieko Matsumura, Keisuke Sugimoto
Publikováno v:
Clinical and Experimental Nephrology. 23(9):1119-1129
Background Hepatocyte nuclear factor 1β(HNF1B), located on chromosome 17q12, causes renal cysts and diabetes syndrome (RCAD). Moreover, various phenotypes related to congenital anomalies of the kidney and urinary tract (CAKUT) or Bartter-like electr
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
Publikováno v:
Internal medicine (Tokyo, Japan). 57(16)
Objective Our aim was to examine the clinical characteristics and phenotype of lipodystrophy of six diabetic Japanese women with partial lipodystrophy (PL) who received a genetic analysis at a diabetic outpatient clinic. Methods We screened for PL us