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

Year Number of Results
2002 7
2003 8
2004 15
2005 6
2006 15
2007 9
2008 6
2009 7
2010 9
2011 11
2012 21
2013 24
2014 27
2015 20
2016 24
2017 23
2018 26
2019 16
2020 21
2021 20
2022 33
2023 16
2024 24

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343 results

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Page 1
TSH resistance revisited.
Narumi S, Hasegawa T. Narumi S, et al. Among authors: hasegawa t. Endocr J. 2015;62(5):393-8. doi: 10.1507/endocrj.EJ15-0131. Epub 2015 Mar 21. Endocr J. 2015. PMID: 25797365 Free article. Review.
Japan Endocrine Society clinical practice guideline for the diagnosis and management of primary aldosteronism 2021.
Naruse M, Katabami T, Shibata H, Sone M, Takahashi K, Tanabe A, Izawa S, Ichijo T, Otsuki M, Omura M, Ogawa Y, Oki Y, Kurihara I, Kobayashi H, Sakamoto R, Satoh F, Takeda Y, Tanaka T, Tamura K, Tsuiki M, Hashimoto S, Hasegawa T, Yoshimoto T, Yoneda T, Yamamoto K, Rakugi H, Wada N, Saiki A, Ohno Y, Haze T. Naruse M, et al. Among authors: hasegawa t. Endocr J. 2022 Apr 28;69(4):327-359. doi: 10.1507/endocrj.EJ21-0508. Epub 2022 Apr 12. Endocr J. 2022. PMID: 35418526 Free article.
[11Beta-hydroxylase deficiency].
Narumi S, Hasegawa T. Narumi S, et al. Among authors: hasegawa t. Nihon Rinsho. 2006 May 28;Suppl 1:699-701. Nihon Rinsho. 2006. PMID: 16776252 Review. Japanese. No abstract available.
[Deprivation dwarfism].
Inokuchi M, Hasegawa T. Inokuchi M, et al. Among authors: hasegawa t. Nihon Rinsho. 2006 May 28;Suppl 1:102-4. Nihon Rinsho. 2006. PMID: 16776104 Review. Japanese. No abstract available.
Cartilage-hair hypoplasia with T-cell dysfunction.
Tomomasa D, Sato T, Hasegawa T, Morio T, Kanegane H. Tomomasa D, et al. Among authors: hasegawa t. Pediatr Int. 2022 Jan;64(1):e15080. doi: 10.1111/ped.15080. Pediatr Int. 2022. PMID: 35278261 No abstract available.
Functional variants in a TTTG microsatellite on 15q26.1 cause familial nonautoimmune thyroid abnormalities.
Narumi S, Nagasaki K, Kiriya M, Uehara E, Akiba K, Tanase-Nakao K, Shimura K, Abe K, Sugisawa C, Ishii T, Miyako K, Hasegawa Y, Maruo Y, Muroya K, Watanabe N, Nishihara E, Ito Y, Kogai T, Kameyama K, Nakabayashi K, Hata K, Fukami M, Shima H, Kikuchi A, Takayama J, Tamiya G, Hasegawa T. Narumi S, et al. Among authors: hasegawa t. Nat Genet. 2024 May;56(5):869-876. doi: 10.1038/s41588-024-01735-5. Epub 2024 May 7. Nat Genet. 2024. PMID: 38714868 Free PMC article.
Whole-exome analysis of 177 pediatric patients with undiagnosed diseases.
Narita K, Muramatsu H, Narumi S, Nakamura Y, Okuno Y, Suzuki K, Hamada M, Yamaguchi N, Suzuki A, Nishio Y, Shiraki A, Yamamori A, Tsumura Y, Sawamura F, Kawaguchi M, Wakamatsu M, Kataoka S, Kato K, Asada H, Kubota T, Muramatsu Y, Kidokoro H, Natsume J, Mizuno S, Nakata T, Inagaki H, Ishihara N, Yonekawa T, Okumura A, Ogi T, Kojima S, Kaname T, Hasegawa T, Saitoh S, Takahashi Y. Narita K, et al. Among authors: hasegawa t. Sci Rep. 2022 Aug 26;12(1):14589. doi: 10.1038/s41598-022-14161-6. Sci Rep. 2022. PMID: 36028527 Free PMC article.
Ruvalcaba syndrome revisited.
Adachi M, Muroya K, Asakura Y, Kurosawa K, Nishimura G, Narumi S, Hasegawa T. Adachi M, et al. Among authors: hasegawa t. Am J Med Genet A. 2010 Jul;152A(7):1854-7. doi: 10.1002/ajmg.a.33429. Am J Med Genet A. 2010. PMID: 20583188 No abstract available.
Destructive thyroiditis without autoantibodies in an infant.
Ichikawa Y, Sato T, Ichihashi Y, Ishii T, Hasegawa T. Ichikawa Y, et al. Among authors: hasegawa t. Pediatr Int. 2022 Jan;64(1):e14709. doi: 10.1111/ped.14709. Epub 2021 Oct 3. Pediatr Int. 2022. PMID: 34605112 No abstract available.
343 results