Researchers Database
KATOU KANAKO
Affiliation： Department of Endocrinology and Metabolism | |||
Last Updated :2026/04/21
Research achievements
Published Papers
- 133, 10-12, Nov. 2017
- 18(8), 743-751, Jun. 2017
- 8(2), 445-449, Apr. 2017
- 41(3), 211-220, Oct. 2014
- 162(5), 309-316, Nov. 2013
- Serum high-molecular-weight adiponectin and response to dapagliflozin in patients with type 2 diabetes and non-alcoholic fatty liver disease., Aso Yoshimasa;Sagara Masaaki;Niitani Takafumi;Kato Kanako;Iijima Toshie;Tomaru Takuya;Jojima Teruo;Usui Isao, Journal of investigative medicine : the official publication of the American Federation for Clinical Research, 69(7), 1324-1329, 20 May 2021
- Serum levels of soluble dipeptidyl peptidase-4 in type 2 diabetes are associated with severity of liver fibrosis evaluated by transient elastography (FibroScan) and the FAST (FibroScan-AST) score, a novel index of non-alcoholic steatohepatitis with significant fibrosis., Sagara Masaaki;Iijima Toshie;Kase Masato;Kato Kanako;Sakurai Shintaro;Tomaru Takuya;Jojima Teruo;Usui Isao;Aso Yoshimasa, Journal of diabetes and its complications, 35(5), 107885, 06 Feb. 2021
- Empagliflozin increases plasma levels of citrulline, histidine, and α-aminobutyric acid in patients with type 2 diabetes: effects of a sodium-glucose co-transporter 2 inhibitor on the plasma amino acid profile., Jojima Teruo;Sakurai Shintaro;Kishi Haruka;Kato Kananko;Iijima Toshie;Tomaru Takuya;Usui Isao;Aso Yoshimasa, Expert opinion on pharmacotherapy, 25(7), 937-944, 04 Jun. 2024
Original paper
- Diabetes with GLP-1R polymorphism (rs3765467) accompanied by myotonic dystrophy: A case of myotonic dystrophy with p.R131Q polymorphism at the glucagon-like peptide-1 receptor (rs3765467) resulting in marked effects of its agonist, dulaglutide., Kato Kanako;Jojima Teruo;Kogai Takahiko;Tanuma Dai;Niitani Takafumi;Sakurai Shintaro;Iijima Toshie;Tomaru Takuya;Usui Isao;Aso Yoshimasa, The American journal of the medical sciences, 369(1), 126-130, 08 Jul. 2024
Review paper
- Genetic alteration of ARMC5 in a patient diagnosed with meningioma and primary macronodular adrenal hyperplasia: a case report., Jojima Teruo;Kogai Takahiko;Iijima Toshie;Kato Kanako;Sagara Masaaki;Kezuka Atsumi;Kase Masato;Sakurai Shintaro;Akimoto Kazumi;Sakumoto Junko;Namatame Takashi;Ueki Keisuke;Hishinuma Akira;Kamai Takao;Usui Isao;Aso Yoshimasa, European journal of endocrinology, 183(6), K7-K12, Dec. 2020
- A case of hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome with a novel frameshift variant in GATA3, p.W10Cfs40, lacks kidney malformation., Kishi Haruka;Jojima Teruo;Kogai Takahiko;Iijima Toshie;Ohira Eriko;Tanuma Dai;Konno Sachiyo;Kato Kanako;Kezuka Atsumi;Akimoto Kazumi;Sakumoto Junko;Hishinuma Akira;Tomaru Takuya;Makita Noriko;Usui Isao;Aso Yoshimasa, Clinical case reports, 8(12), 2619-2624, Dec. 2020
Case report
- Evaluation of thumbnail clipping as a specimen for retrospectively assessing average production of testosterone., Higashi Tatsuya;Aso Saki;Horisaki Hiroaki;Ito Takenori;Tanaka Sakurako;Nishimoto-Kusunose Shoichi;Ogawa Shoujiro;Kato Kazuhiko;Ide Hisamitsu, Clinica chimica acta; international journal of clinical chemistry, 538, 157-163, 20 Nov. 2022
Unclear