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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 2
2011 3
2012 4
2013 1
2014 1
2015 2
2016 1
2017 2
2018 2
2019 1
2020 1
2021 3
2022 1
2023 1
2024 1

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23 results

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Page 1
Prospective Multicenter Registry-Based Study on Thyroid Storm: The Guidelines for the Management from Japan are Useful.
Furukawa Y, Tanaka K, Isozaki O, Suzuki A, Iburi T, Tsuboi K, Iguchi M, Kanamoto N, Minamitani K, Wakino S, Satoh T, Teramukai S, Kimura E, Miyake Y, Akamizu T. Furukawa Y, et al. Among authors: minamitani k. J Clin Endocrinol Metab. 2024 Mar 8:dgae124. doi: 10.1210/clinem/dgae124. Online ahead of print. J Clin Endocrinol Metab. 2024. PMID: 38454797
Guidelines for Newborn Screening of Congenital Hypothyroidism (2021 Revision).
Nagasaki K, Minamitani K, Nakamura A, Kobayashi H, Numakura C, Itoh M, Mushimoto Y, Fujikura K, Fukushi M, Tajima T. Nagasaki K, et al. Among authors: minamitani k. Clin Pediatr Endocrinol. 2023;32(1):26-51. doi: 10.1297/cpe.2022-0063. Epub 2022 Dec 4. Clin Pediatr Endocrinol. 2023. PMID: 36761493 Free PMC article.
Erythematous Plaques in a Child with Sweet Syndrome.
Aoki T, Yamashita Y, Minamitani K, Ota S, Hayakawa K. Aoki T, et al. Among authors: minamitani k. J Pediatr. 2016 Sep;176:210-210.e1. doi: 10.1016/j.jpeds.2016.05.055. Epub 2016 Jun 16. J Pediatr. 2016. PMID: 27318383 No abstract available.
Guidelines for the treatment of childhood-onset Graves' disease in Japan, 2016.
Committee on Pharmaceutical Affairs, Japanese Society for Pediatric Endocrinology, and the Pediatric Thyroid Disease Committee, Japan Thyroid Association (Taskforce for the Revision of the Guidelines for the Treatment of Childhood-Onset Graves’ Disease); Minamitani K, Sato H, Ohye H, Harada S, Arisaka O. Committee on Pharmaceutical Affairs, Japanese Society for Pediatric Endocrinology, and the Pediatric Thyroid Disease Committee, Japan Thyroid Association (Taskforce for the Revision of the Guidelines for the Treatment of Childhood-Onset Graves’ Disease), et al. Among authors: minamitani k. Clin Pediatr Endocrinol. 2017;26(2):29-62. doi: 10.1297/cpe.26.29. Epub 2017 Apr 22. Clin Pediatr Endocrinol. 2017. PMID: 28458457 Free PMC article.
Clinical characteristics of septo-optic dysplasia accompanied by congenital central hypothyroidism in Japan.
Nagasaki K, Kubota T, Kobayashi H, Sawada H, Numakura C, Harada S, Takasawa K, Minamitani K, Ishii T, Okada S, Kamasaki H, Sugihara S, Adachi M, Tajima T. Nagasaki K, et al. Among authors: minamitani k. Clin Pediatr Endocrinol. 2017;26(4):207-213. doi: 10.1297/cpe.26.207. Epub 2017 Sep 28. Clin Pediatr Endocrinol. 2017. PMID: 29026269 Free PMC article.
Guidelines for diagnosis and treatment of 21-hydroxylase deficiency (2014 revision).
Mass Screening Committee; Japanese Society for Pediatric Endocrinology; Japanese Society for Mass Screening; Ishii T, Anzo M, Adachi M, Onigata K, Kusuda S, Nagasaki K, Harada S, Horikawa R, Minagawa M, Minamitani K, Mizuno H, Yamakami Y, Fukushi M, Tajima T. Mass Screening Committee, et al. Among authors: minamitani k. Clin Pediatr Endocrinol. 2015 Jul;24(3):77-105. doi: 10.1297/cpe.24.77. Epub 2015 Jul 18. Clin Pediatr Endocrinol. 2015. PMID: 26594092 Free PMC article.
23 results