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

Year Number of Results
1972 1
1994 3
1995 1
1996 3
1997 1
1998 3
1999 1
2000 3
2001 4
2002 5
2003 1
2004 1
2005 3
2006 2
2007 2
2008 2
2009 4
2010 3
2011 6
2012 8
2013 12
2014 13
2015 11
2016 20
2017 14
2018 12
2019 11
2020 17
2021 22
2022 24
2023 13
2024 6

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198 results

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Page 1
[Congenital thrombocytopenia].
Sasahara Y. Sasahara Y. Rinsho Ketsueki. 2021;62(8):1319-1326. doi: 10.11406/rinketsu.62.1319. Rinsho Ketsueki. 2021. PMID: 34497222 Japanese.
Twenty-Year Change in Severity and Outcome of Ischemic and Hemorrhagic Strokes.
Toyoda K, Yoshimura S, Nakai M, Koga M, Sasahara Y, Sonoda K, Kamiyama K, Yazawa Y, Kawada S, Sasaki M, Terasaki T, Miwa K, Koge J, Ishigami A, Wada S, Iwanaga Y, Miyamoto Y, Minematsu K, Kobayashi S; Japan Stroke Data Bank Investigators. Toyoda K, et al. Among authors: sasahara y. JAMA Neurol. 2022 Jan 1;79(1):61-69. doi: 10.1001/jamaneurol.2021.4346. JAMA Neurol. 2022. PMID: 34870689 Free PMC article.
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: sasahara y. 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.
Phenotypic heterogeneity in individuals with MECOM variants in 2 families.
Niihori T, Tanoshima R, Sasahara Y, Sato A, Irie M, Saito-Nanjo Y, Funayama R, Shirota M, Abe T, Okuyama Y, Ishii N, Nakayama K, Kure S, Imaizumi M, Aoki Y. Niihori T, et al. Among authors: sasahara y. Blood Adv. 2022 Sep 27;6(18):5257-5261. doi: 10.1182/bloodadvances.2020003812. Blood Adv. 2022. PMID: 35020829 Free PMC article. No abstract available.
Characteristic phenotypes of ADH5/ALDH2 deficiency during childhood.
Matsumoto M, Oyake M, Itonaga T, Maeda M, Suenobu S, Sato D, Sasahara Y, Mishima H, Yoshiura KI, Ihara K. Matsumoto M, et al. Among authors: sasahara y. Eur J Med Genet. 2024 Apr 15;69:104939. doi: 10.1016/j.ejmg.2024.104939. Online ahead of print. Eur J Med Genet. 2024. PMID: 38614309 Free article.
Clofarabine monotherapy in two patients with refractory Langerhans cell histiocytosis.
Irie M, Nakano T, Katayama S, Suzuki T, Moriya K, Watanabe Y, Suzuki N, Saitoh-Nanjyo Y, Onuma M, Rikiishi T, Niizuma H, Sasahara Y, Kure S. Irie M, et al. Among authors: sasahara y. Cancer Rep (Hoboken). 2022 Aug;5(8):e1579. doi: 10.1002/cnr2.1579. Epub 2021 Nov 1. Cancer Rep (Hoboken). 2022. PMID: 34725963 Free PMC article.
198 results