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

Year Number of Results
1987 2
1988 3
1989 4
1990 8
1991 8
1992 7
1993 8
1994 8
1995 11
1996 4
1997 6
1998 6
1999 9
2000 8
2001 9
2002 9
2003 8
2004 12
2005 16
2006 18
2007 15
2008 17
2009 14
2010 19
2011 16
2012 16
2013 26
2014 22
2015 29
2016 29
2017 34
2018 60
2019 57
2020 46
2021 63
2022 46
2023 53
2024 19

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649 results

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Page 1
Updated guidelines for chronic active Epstein-Barr virus disease.
Kawada JI, Ito Y, Ohshima K, Yamada M, Kataoka S, Muramatsu H, Sawada A, Wada T, Imadome KI, Arai A, Iwatsuki K, Ohga S, Kimura H; Committee for Guidelines for the Management of Chronic Active EBV Disease, Related Disorders (the MHLW Research Team in Japan). Kawada JI, et al. Among authors: ohga s. Int J Hematol. 2023 Nov;118(5):568-576. doi: 10.1007/s12185-023-03660-5. Epub 2023 Sep 20. Int J Hematol. 2023. PMID: 37728704 Free PMC article. Review.
Human RELA dominant-negative mutations underlie type I interferonopathy with autoinflammation and autoimmunity.
Moriya K, Nakano T, Honda Y, Tsumura M, Ogishi M, Sonoda M, Nishitani-Isa M, Uchida T, Hbibi M, Mizoguchi Y, Ishimura M, Izawa K, Asano T, Kakuta F, Abukawa D, Rinchai D, Zhang P, Kambe N, Bousfiha A, Yasumi T, Boisson B, Puel A, Casanova JL, Nishikomori R, Ohga S, Okada S, Sasahara Y, Kure S. Moriya K, et al. Among authors: ohga s. J Exp Med. 2023 Sep 4;220(9):e20212276. doi: 10.1084/jem.20212276. Epub 2023 Jun 5. J Exp Med. 2023. PMID: 37273177 Free PMC article.
β-d-Gulose.
Ishii T, Ohga S, Fukada K, Morimoto K, Sakane G. Ishii T, et al. Among authors: ohga s. Acta Crystallogr Sect E Struct Rep Online. 2014 Apr 16;70(Pt 5):o569. doi: 10.1107/S1600536814008046. eCollection 2014 May 1. Acta Crystallogr Sect E Struct Rep Online. 2014. PMID: 24860374 Free PMC article.
Molecular diagnosis of 405 individuals with autism spectrum disorder.
Miyake N, Tsurusaki Y, Fukai R, Kushima I, Okamoto N, Ohashi K, Nakamura K, Hashimoto R, Hiraki Y, Son S, Kato M, Sakai Y, Osaka H, Deguchi K, Matsuishi T, Takeshita S, Fattal-Valevski A, Ekhilevitch N, Tohyama J, Yap P, Keng WT, Kobayashi H, Takubo K, Okada T, Saitoh S, Yasuda Y, Murai T, Nakamura K, Ohga S, Matsumoto A, Inoue K, Saikusa T, Hershkovitz T, Kobayashi Y, Morikawa M, Ito A, Hara T, Uno Y, Seiwa C, Ishizuka K, Shirahata E, Fujita A, Koshimizu E, Miyatake S, Takata A, Mizuguchi T, Ozaki N, Matsumoto N. Miyake N, et al. Among authors: ohga s. Eur J Hum Genet. 2023 Mar 27. doi: 10.1038/s41431-023-01335-7. Online ahead of print. Eur J Hum Genet. 2023. PMID: 36973392
[Diabetic nephropathy].
Ohga S, Shikata K, Makino H. Ohga S, et al. Nihon Rinsho. 2005 Mar;63 Suppl 3:155-60. Nihon Rinsho. 2005. PMID: 15813061 Free article. Review. Japanese. No abstract available.
De novo ATP1A3 variants cause polymicrogyria.
Miyatake S, Kato M, Kumamoto T, Hirose T, Koshimizu E, Matsui T, Takeuchi H, Doi H, Hamada K, Nakashima M, Sasaki K, Yamashita A, Takata A, Hamanaka K, Satoh M, Miyama T, Sonoda Y, Sasazuki M, Torisu H, Hara T, Sakai Y, Noguchi Y, Miura M, Nishimura Y, Nakamura K, Asai H, Hinokuma N, Miya F, Tsunoda T, Togawa M, Ikeda Y, Kimura N, Amemiya K, Horino A, Fukuoka M, Ikeda H, Merhav G, Ekhilevitch N, Miura M, Mizuguchi T, Miyake N, Suzuki A, Ohga S, Saitsu H, Takahashi H, Tanaka F, Ogata K, Ohtaka-Maruyama C, Matsumoto N. Miyatake S, et al. Among authors: ohga s. Sci Adv. 2021 Mar 24;7(13):eabd2368. doi: 10.1126/sciadv.abd2368. Print 2021 Mar. Sci Adv. 2021. PMID: 33762331 Free PMC article.
649 results