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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 19
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392 results
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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; 1993–2022. 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; 1993–2022. 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.
SAMD9 mutations cause a novel multisystem disorder, MIRAGE syndrome, and are associated with loss of chromosome 7.
Narumi S, Amano N, Ishii T, Katsumata N, Muroya K, Adachi M, Toyoshima K, Tanaka Y, Fukuzawa R, Miyako K, Kinjo S, Ohga S, Ihara K, Inoue H, Kinjo T, Hara T, Kohno M, Yamada S, Urano H, Kitagawa Y, Tsugawa K, Higa A, Miyawaki M, Okutani T, Kizaki Z, Hamada H, Kihara M, Shiga K, Yamaguchi T, Kenmochi M, Kitajima H, Fukami M, Shimizu A, Kudoh J, Shibata S, Okano H, Miyake N, Matsumoto N, Hasegawa T. Narumi S, et al. Nat Genet. 2016 Jul;48(7):792-7. doi: 10.1038/ng.3569. Epub 2016 May 16. Nat Genet. 2016. PMID: 27182967
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.
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.
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.
Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients.
Inoue T, Nakamura A, Iwahashi-Odano M, Tanase-Nakao K, Matsubara K, Nishioka J, Maruo Y, Hasegawa Y, Suzumura H, Sato S, Kobayashi Y, Murakami N, Nakabayashi K, Yamazawa K, Fuke T, Narumi S, Oka A, Ogata T, Fukami M, Kagami M. Inoue T, et al. Among authors: narumi s. Clin Epigenetics. 2020 Jun 16;12(1):86. doi: 10.1186/s13148-020-00865-x. Clin Epigenetics. 2020. PMID: 32546215 Free PMC article.
[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.
392 results