Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Ikuo Yamamori"'
Publikováno v:
Endocrine Journal, Vol 71, Iss 10, Pp 1003-1011 (2024)
A 38-year-old Japanese woman with a history of abnormal thyroid function of non-autoimmune origin, pituitary endocrine tumor, and untreated diabetes mellitus was referred to our outpatient clinic when she became pregnant with twins. Physical findings
Externí odkaz:
https://doaj.org/article/0a406d7d575d42f0b372e88a0b44afb1
Autor:
Tatsuo Ishizuka, Yasuhiro Hakamata, Mashio Nakamura, Toshio Hayashi, Hiroshi Morita, Kazuhiko Nishigaki, Ikuo Yamamori, Hiroyuki Morita
Publikováno v:
Nihon Naika Gakkai Zasshi. 101:2342-2349
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::033ecdca52c3f59d45a228211662492c
https://doi.org/10.2169/naika.101.2342
https://doi.org/10.2169/naika.101.2342
Autor:
Yoshihiro Inamoto, Noriyuki Hirabayashi, Koichi Miyamura, Takaomi Sanda, Koji Shirai, Yoshihisa Kodera, Tamio Teramoto, Hideko Tsukamoto, Ikuo Yamamori
Publikováno v:
International Journal of Hematology. 82:362-366
A 55-year-old woman with Ph-negative acute lymphoblastic leukemia in primary induction failure received allogeneic peripheral blood stem cell transplantation from her HLA-compatible sister. Pseudohyponatremia developed due to extreme hypercholesterol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2733eead9a827d9ae0ba5735ec344f5
https://doi.org/10.1532/ijh97.05064
https://doi.org/10.1532/ijh97.05064
Autor:
Ikuo Yamamori, Tsuyoshi Yokoi, Mitsuo Yamaki, Yui Yamamoto, M. Suzuki, Takanobu Wakasugi, Ayaka Shibata, Noriaki Shimada, Hiroshi Yamazaki, Miki Nakajima
Publikováno v:
Drug Metabolism and Pharmacokinetics. 16:145-150
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfc06b27a610904d8463057f07ffca72
https://doi.org/10.2133/dmpk.16.145
https://doi.org/10.2133/dmpk.16.145
Autor:
Tetsuya Nagatani, Masako Yamauchi, Fumiko Yamakawa, Akihiro Hirakawa, Tsutomu Yamada, Yuko Yambe, Yutaka Oiso, Masazumi Fujii, Takashi Murase, Ikuo Yamamori, Toshihiko Wakabayashi, Hiroshi Arima
Publikováno v:
Endocrine journal. 61(2)
Central diabetes insipidus (CDI) is caused by deficiency of arginine vasopressin, an antidiuretic hormone. Patients with CDI manifest polyuria which is usually compensated for by increases in water intake. However, some patients are not able to sense
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e258c3aacca90294b6c23cf4bf9ab4d6
https://pubmed.ncbi.nlm.nih.gov/24212879
https://pubmed.ncbi.nlm.nih.gov/24212879
Autor:
Ikuo Yamamori, Yuichi Kumahara, Tsukasa Noguchi, Tokuo Nakajima, Junta Takamatsu, Yuichi Mori
Publikováno v:
Internal Medicine. 32:6-9
Complete thyroxine-binding globulin deficiency (TBG-CD) was uncovered in a subject receiving a comprehensive health examination. The subject had an abnormally high T3 resin uptake. A family study showed that the TBG abnormality had been inherited by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fcc4463d7dc7dd6a93d47cec15cfb56
https://doi.org/10.2169/internalmedicine.32.6
https://doi.org/10.2169/internalmedicine.32.6
Autor:
Yuichi Mori, Hisao Seo, Yoshiyuki Tani, Yoshitaka Miura, Yutaka Oiso, Ikuo Yamamori, Shuji Imamura
Publikováno v:
Endocrine Journal. 40:563-569
Thyroxine-binding globulin (TBG) is a major thyroid hormone transport protein in human serum. Its complete deficiency (TBG-CD) is one of inherited TBG abnormalities that transmit on X-chromosome. We previously reported a nucleotide deletion at codon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e262b52732c1adea7d41b74b0ac8f59
https://doi.org/10.1507/endocrj.40.563
https://doi.org/10.1507/endocrj.40.563
Autor:
Shinji Susa, Hideo Sasaki, Masao Kondo, Keiichi Yamatani, Takeo Kato, Ikuo Yamamori, Makoto Daimon
Publikováno v:
Journal of Human Genetics. 43:182-184
Hereditary coproporphyria (HCP) is an autosomal dominant disease characterized by a deficiency of coproporphyrinogen oxidase (CPO). Only 11 mutations of the gene have been reported to date as the mutations responsible for HCP. We report here a novel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a27ab7f06ee1d9bbed23bba0c231997f
https://doi.org/10.1007/s100380050065
https://doi.org/10.1007/s100380050065
Autor:
Takanobu Wakasugi, Ayaka Shibata, Ikuo Yamamori, Rawiwan Maniratanachote, Shogo Tokudome, Miki Nakajima, Shuichi Kaneko, Kanefusa Katoh, Tsuyoshi Yokoi, Takeshi Sawazaki
Publikováno v:
Toxicology. 216(1)
Troglitazone is a thiazolidinedione antidiabetic agent with insulin-sensitizing activities that was withdrawn from the market in 2000 due to its association with idiosyncratic hepatotoxicity. To address the suspected autoantibody production associate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d45313de0bbc4da921c852ba567e70d2
https://pubmed.ncbi.nlm.nih.gov/16115720
https://pubmed.ncbi.nlm.nih.gov/16115720