Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Dai Tanuma"'
Autor:
Teruo Jojima, Hidetaka Kurai, Dai Tanuma, Hayato Kajitani, Masato Kase, Yuiko Inoue, Shintaro Sakurai, Toshie Iijima, Takuya Tomaru, Isao Usui, Yoshimasa Aso
Publikováno v:
International Journal of Cardiology: Heart & Vasculature, Vol 41, Iss , Pp 101071- (2022)
Aims: To investigate synergistic effects of liver fibrosis evaluated by FibroScan and sarcopenia on endothelial function and arterial stiffness in patients with type 2 diabetes. Methods: This cross-sectional study evaluated liver fibrosis (LF) and sa
Externí odkaz:
https://doaj.org/article/2695e616ff0c468e812fe6f609a56b83
Autor:
Haruka Kishi, Teruo Jojima, Takahiko Kogai, Toshie Iijima, Eriko Ohira, Dai Tanuma, Sachiyo Konno, Kanako Kato, Atsumi Kezuka, Kazumi Akimoto, Junko Sakumoto, Akira Hishinuma, Takuya Tomaru, Noriko Makita, Isao Usui, Yoshimasa Aso
Publikováno v:
Clinical Case Reports, Vol 8, Iss 12, Pp 2619-2624 (2020)
Abstract Autosomal dominant hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome are typically diagnosed by manifestations of the three features with a positive family history. Our case carried a de novo variant in causative gene, GATA3,
Externí odkaz:
https://doaj.org/article/43c5c4f10fc74e1891a01b40795994bd
Autor:
Nanako Hirao, Toshie Iijima, Dai Tanuma, Eriko Ohira, Hidetaka Kurai, Toshimitsu Shinzawa, Masato Kase, Shintaro Sakurai, Takuya Tomaru, Teruo Jojima, Isao Usui, Yoshimasa Aso
Publikováno v:
Clinical Endocrinology. 97:841-848
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dce3fa9d5e955ae520aff04aa68ebab7
https://doi.org/10.1111/cen.14788
https://doi.org/10.1111/cen.14788
Autor:
Sachiyo Konno, Dai Tanuma, Eriko Ohira, Takahiko Kogai, Takuya Tomaru, Isao Usui, Teruo Jojima, Akira Hishinuma, Junko Sakumoto, Haruka Kishi, Kazumi Akimoto, Yoshimasa Aso, Atsumi Kezuka, Toshie Iijima, Noriko Makita, Kanako Kato
Publikováno v:
Clinical Case Reports, Vol 8, Iss 12, Pp 2619-2624 (2020)
Clinical Case Reports
Clinical Case Reports
Autosomal dominant hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome are typically diagnosed by manifestations of the three features with a positive family history. Our case carried a de novo variant in causative gene, GATA3, but prese
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08e17545ebfbbed64bca9bcb780ab639
https://doaj.org/article/43c5c4f10fc74e1891a01b40795994bd
https://doaj.org/article/43c5c4f10fc74e1891a01b40795994bd
Autor:
Nanako, Hirao, Toshie, Iijima, Dai, Tanuma, Eriko, Ohira, Hidetaka, Kurai, Toshimitsu, Shinzawa, Masato, Kase, Shintaro, Sakurai, Takuya, Tomaru, Teruo, Jojima, Isao, Usui, Yoshimasa, Aso
Publikováno v:
Clinical endocrinologyREFERENCES. 97(6)
We investigated longitudinal changes in circulating CD4sup+/supand CD8sup+/supT cells positive for programed cell death protein-1 (PD-1) and in other subsets of CD4sup+/supT cells in untreated hyperthyroid patients with Graves' disease after treatmen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b7bd26d239c67bd3380ebb1c7cf4bed1
https://pubmed.ncbi.nlm.nih.gov/35692119
https://pubmed.ncbi.nlm.nih.gov/35692119