Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Satoru Sakihara"'
Autor:
Noriko Kimura, Yasuji Hirata, Nozomu Iwashiro, Hiroshi Kijima, Shinobu Takayasu, Satoshi Yamagata, Satoru Sakihara, Shinya Uchino, Masanori Ohara
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
BackgroundMultiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterized by the occurrence of multiple epithelial neuroendocrine tumors (NETs) and non-NETs in various organs. MEN1 encodes a 610-amino acid-long tumor suppre
Externí odkaz:
https://doaj.org/article/1ea0a8a8732c4ae0adbf27117c7bb8d9
Autor:
Satoshi Konno, Tomonori Satoh, Satoru Sakihara, Takako Takahashi, Masanori Munakata, Yuki Nemoto, Shigefumi Suzuki, Tomomi Hattori
Publikováno v:
Internal Medicine
Objective We aimed to examine the effects of isometric handgrip (IHG) training on home blood pressure (BP) levels in hypertensive Japanese patients undergoing treatment. Methods Fifty-three hypertensive patients (mean age, 61.7 years; 56.6% men) with
Autor:
Kazunori Kageyama, Ken Terui, Makoto Daimon, Satoru Sakihara, Aya Sugiyama, Shinobu Takayasu, Wataru Kameda
Publikováno v:
Endocrine journal. 65(10)
Thyrotropin (TSH)-producing adenomas are a rare cause of hyperthyroidism and are a type of functional pituitary adenoma. The diagnosis of TSH-producing adenoma is a challenging problem in clinical endocrinology. Since growth hormone-releasing peptide
Autor:
Akira Kurose, Masanori Hisaoka, Yuki Fujita, Sotai Kimura, Michiro Yanagisawa, Satoru Sakihara
Publikováno v:
Pathology International. 65:510-512
Publikováno v:
Endocrine Journal. 60:127-135
Adrenocorticotropic hormone (ACTH)-dependent Cushing's syndrome is caused by an ACTH-producing tumor, as is the case with Cushing's disease and ectopic ACTH syndrome (EAS). Diagnosis and differential diagnosis of Cushing's disease from EAS in ACTH-de
Autor:
Jingbo Huang, Athanasios Soskos, Safwan M. Murad, Bruce R. Krawisz, Steven H. Yale, Andrew C. Urquhart, Tae H. Lee, Abid Yaqub, James Norweck, Monjur Ahmed, Narayanan Kandasamy, Graham Lennox, Anand K. Annamalai, Gerald Maguire, Amanda I. Adler, Priscilla Mutharasan, Wendy Oatis, Hau Kwaan, Mark Molitch, Hagig Mazeh, Pasithorn A. Suwanabol, David F. Schneider, Rebecca S. Sippel, Sheela Subramanyam, Robert A. Kreisberg, Patrick B. O’Neal, Francis D. Moore Jr, Atul Gawande, Nancy L. Cho, Jacob Moalem, Daniel T. Ruan, Jennifer Y. Han, Leili Mirsadraei, Michael W. Yeh, Jeffrey D. Suh, William H. Yong, Marvin Bergsneider, Anthony P. Heaney, Yuki Kikuchi, Ryuichi Wada, Satoru Sakihara, Toshihiro Suda, Soroku Yagihashi
Publikováno v:
Endocrine Practice. 18:563-566
Autor:
Komaki Hanada, Minoru Yasujima, Satoru Sakihara, Toshihiro Suda, Kazunori Kageyama, Mihoko Kushibiki
Publikováno v:
Regulatory Peptides. 158:116-120
Growth hormone (GH)-releasing peptides (GHRPs) are synthetic peptides which induce strong GH release in both animals and humans. Among them, GHRP-2 is known to stimulate GH release by acting at both hypothalamic and pituitary sites, but also induces
Autor:
Ken Tomotsune, Toshihiro Suda, Kazunori Kageyama, Yuko Tsushima, Satoru Sakihara, Miyuki Yanagimachi
Publikováno v:
Internal Medicine. 48:607-610
Growth hormone (GH) deficiency is transient in most cases of adrenocorticotropin (ACTH) deficiency, while deficiency of both selective ACTH and GH in adults, as in the present case, is rare among hypopituitarism cases. In this patient, one year after
Autor:
Ken Terui, Kazunori Kageyama, Hironobu Sasano, Chikara Ohyama, Shinobu Takayasu, Toshihiro Suda, Shingo Hatakeyama, Satoru Sakihara, Takeshi Nigawara
Publikováno v:
Internal Medicine. 48:235-240
A 68-year-old woman was referred for characterization of a left adrenal incidentaloma. Endocrinological examinations indicated subclinical Cushing's syndrome, whereas the large volume (10 cm in diameter) and heterogeneous configuration of the tumor r
Autor:
Shinobu Takayasu, Takeshi Usui, Satoru Sakihara, Hironobu Sasano, Toshihiro Suda, Takeshi Nigawara, Masayuki Kawahara, Kazunori Kageyama, Chikara Ohyama, Atsushi Imai
Publikováno v:
Endocrine Journal. 55:291-297
Nonclassical form of 21-hydroxylase deficiency (NC 21OHD) as a frequent variant on the milder end of the disease spectrum has been widely acknowledged, but its potential contribution to adrenocortical tumorigenesis has not been fully elucidated. We r