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Results by year

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

Year Number of Results
1965 1
1967 1
1968 1
1970 1
1972 2
1973 2
1974 1
1976 1
1977 1
1978 6
1979 3
1980 1
1981 2
1982 1
1983 5
1984 4
1985 11
1986 2
1987 4
1988 2
1989 4
1990 3
1991 1
1992 2
1993 2
1994 1
1995 2
1996 1
1997 2
1998 5
1999 6
2000 7
2001 7
2002 7
2003 6
2004 13
2005 5
2006 7
2007 8
2008 16
2009 6
2010 11
2011 8
2012 18
2013 9
2014 18
2015 17
2016 27
2017 27
2018 31
2019 18
2020 34
2021 29
2022 26
2023 2
Text availability
Article attribute
Article type
Publication date

Search Results

400 results
Results by year
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Page 1
MIRAGE Syndrome.
Tanase-Nakao K, Olson TS, Narumi S. Tanase-Nakao K, et al. Among authors: narumi s. 2020 Nov 25. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. 2020 Nov 25. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. PMID: 33237688 Free Books & Documents. Review.
Germline loss-of-function SAMD9 and SAMD9L alterations in adult myelodysplastic syndromes.
Nagata Y, Narumi S, Guan Y, Przychodzen BP, Hirsch CM, Makishima H, Shima H, Aly M, Pastor V, Kuzmanovic T, Radivoyevitch T, Adema V, Awada H, Yoshida K, Li S, Sole F, Hanna R, Jha BK, LaFramboise T, Ogawa S, Sekeres MA, Wlodarski MW, Cammenga J, Maciejewski JP. Nagata Y, et al. Among authors: narumi s. Blood. 2018 Nov 22;132(21):2309-2313. doi: 10.1182/blood-2017-05-787390. Epub 2018 Oct 15. Blood. 2018. PMID: 30322869 Free PMC article. No abstract available.
Discovery of MIRAGE syndrome.
Narumi S. Narumi S. Pediatr Int. 2022 Jan;64(1):e15283. doi: 10.1111/ped.15283. Pediatr Int. 2022. PMID: 35972063 Review.
TSH resistance revisited.
Narumi S, Hasegawa T. Narumi S, et al. 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.
[11Beta-hydroxylase deficiency].
Narumi S, Hasegawa T. Narumi S, et al. Nihon Rinsho. 2006 May 28;Suppl 1:699-701. Nihon Rinsho. 2006. PMID: 16776252 Review. Japanese. No abstract available.
Role of Liquid-Liquid Separation in Endocrine and Living Cells.
Akiba K, Katoh-Fukui Y, Yoshida K, Narumi S, Miyado M, Hasegawa Y, Fukami M. Akiba K, et al. Among authors: narumi s. J Endocr Soc. 2021 Jul 19;5(10):bvab126. doi: 10.1210/jendso/bvab126. eCollection 2021 Oct 1. J Endocr Soc. 2021. PMID: 34396024 Free PMC article. Review.
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: narumi s. 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: narumi s. 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.
400 results