Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Rei Hirose"'
Autor:
Jaeduk Yoshimura Noh, Kosuke Inoue, Nami Suzuki, Ai Yoshihara, Miho Fukushita, Masako Matsumoto, Hideyuki Imai, Shigenori Hiruma, Masahiro Ichikawa, Masakazu Koshibu, Akiko Sankoda, Rei Hirose, Natsuko Watanabe, Kiminori Sugino, Koichi Ito
Publikováno v:
Endocrine Journal, Vol 71, Iss 7, Pp 695-703 (2024)
Agranulocytosis is a serious adverse effect of methimazole (MMI) and propylthiouracil (PTU), and although there have been reports suggesting a dose-dependent incidence in relation to both drugs, the evidence has not been conclusive. The objective of
Externí odkaz:
https://doaj.org/article/2c9df66a660949b9b940fac9ff8396e4
Autor:
Yuko Kiyohara, Rei Hirose, Hiroshi Kawamata, Kazuki Nakai, Akane Hirataka, Jun Saito, Yuya Tsurutani
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-5 (2023)
Fibromuscular dysplasia can cause renovascular hypertension. Since fibromuscular dysplasia may be underdiagnosed, precise diagnosis and management are crucial, especially for young women. A 20-year-old woman with hypertension and hypokalemia was refe
Externí odkaz:
https://doaj.org/article/d48093c7587a45d7add14e6bc0de7768
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-5 (2023)
A 42-year-old female patient was referred to our hospital with hypertension and hypokalemia and was diagnosed with primary aldosteronism. Dynamic contrast-enhanced computed tomography images revealed a 13-mm nodule on the lateral segment of the left
Externí odkaz:
https://doaj.org/article/9365b3d096334df8ad5f2e3a5d80ff04
Autor:
Rei Hirose, Yuya Tsurutani, Chiho Sugisawa, Kosuke Inoue, Sachiko Suematsu, Maki Nagata, Naoki Hasegawa, Yukio Kakuta, Masato Yonamine, Kazuhiro Takekoshi, Noriko Kimura, Jun Saito, Tetsuo Nishikawa
Publikováno v:
Journal of Medical Case Reports, Vol 15, Iss 1, Pp 1-8 (2021)
Abstract Background Pheochromocytoma and paraganglioma caused by succinate dehydrogenase gene mutations is called hereditary pheochromocytoma/paraganglioma syndrome. In particular, succinate dehydrogenase subunit B mutations are important because the
Externí odkaz:
https://doaj.org/article/b88ab9f5b455418e9d574877194a7475
Autor:
Haremaru Kubo, Yuya Tsurutani, Kosuke Inoue, Kazuki Watanabe, Yuto Yamazaki, Takashi Sunouchi, Yoshitomo Hoshino, Rei Hirose, Sho Katsuragawa, Hiromitsu Tannai, Yukiko Shibahara, Yukio Kakuta, Seishi Matsui, Jun Saito, Masao Omura, Hironobu Sasano, Tetsuo Nishikawa
Publikováno v:
PLoS ONE, Vol 17, Iss 4, p e0267732 (2022)
Primary aldosteronism (PA) usually accompanies suppressed plasma renin activity (PRA) through a negative feedback mechanism. While some cases of PA with unsuppressed PRA were reported, there have been no studies about the characteristics of PA with u
Externí odkaz:
https://doaj.org/article/cb6b2541ded04138b995959c602fca4b
Autor:
Haremaru Kubo, Yuya Tsurutani, Takashi Sunouchi, Yoshitomo Hoshino, Rei Hirose, Sho Katsuragawa, Noriko Kimura, Jun Saito, Tetsuo Nishikawa
Publikováno v:
Journal of Clinical Medicine, Vol 11, Iss 15, p 4624 (2022)
Pheochromocytoma (PCC) is rare catecholamine-producing endocrine tumor that metastasizes in approximately 10% of cases. As a functional imaging of PCC, 123I-metaiodobenzylguanidine (MIBG) scintigraphy was established, and some cases of PCC exhibit ne
Externí odkaz:
https://doaj.org/article/c86b83c5bf5d4e12b8741492fbec4091
Publikováno v:
Internal Medicine; 2024, Vol. 63 Issue 10, p1405-1413, 9p
Autor:
Takuhei, Hitsuwari, Yuya, Tsurutani, Takahiro, Yamane, Takashi, Sunouchi, Hirofumi, Horikoshi, Rei, Hirose, Yoshitomo, Hoshino, Satoshi, Watanabe, Sho, Katsuragawa, Jun, Saitou
Publikováno v:
Internal Medicine. 61:3069-3075
Thyrotoxicosis and sodium-glucose transport protein 2 inhibitors (SGLT2is) are associated with the induction of euglycemic diabetic ketoacidosis (euDKA). We herein report two cases of euDKA in patients with diabetes mellitus wherein both thyrotoxicos
Publikováno v:
The Tohoku Journal of Experimental Medicine. 257:337-345
Autor:
Kazuhiro Takekoshi, Tetsuo Nishikawa, Naoki Hasegawa, Jun Saito, Masato Yonamine, Noriko Kimura, Kosuke Inoue, Chiho Sugisawa, Rei Hirose, Yukio Kakuta, Sachiko Suematsu, Yuya Tsurutani, Maki Nagata
Publikováno v:
Journal of Medical Case Reports, Vol 15, Iss 1, Pp 1-8 (2021)
Journal of Medical Case Reports
Journal of Medical Case Reports
Background Pheochromocytoma and paraganglioma caused by succinate dehydrogenase gene mutations is called hereditary pheochromocytoma/paraganglioma syndrome. In particular, succinate dehydrogenase subunit B mutations are important because they are str