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

Year Number of Results
1965 1
1968 1
1969 2
1974 1
1975 4
1978 1
1981 1
1982 1
1983 2
1985 3
1986 5
1987 8
1988 6
1989 8
1990 5
1991 6
1992 7
1993 9
1994 7
1995 11
1996 3
1997 8
1998 12
1999 13
2000 10
2001 6
2003 1
2008 1
2010 1
2011 2
2012 4
2013 9
2014 11
2015 5
2016 7
2017 8
2018 6
2019 10
2020 14
2021 9
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Publication date

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216 results
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Page 1
Clinicopathological features of adult-onset neuronal intranuclear inclusion disease.
Sone J, Mori K, Inagaki T, Katsumata R, Takagi S, Yokoi S, Araki K, Kato T, Nakamura T, Koike H, Takashima H, Hashiguchi A, Kohno Y, Kurashige T, Kuriyama M, Takiyama Y, Tsuchiya M, Kitagawa N, Kawamoto M, Yoshimura H, Suto Y, Nakayasu H, Uehara N, Sugiyama H, Takahashi M, Kokubun N, Konno T, Katsuno M, Tanaka F, Iwasaki Y, Yoshida M, Sobue G. Sone J, et al. Among authors: kurashige t. Brain. 2016 Dec;139(Pt 12):3170-3186. doi: 10.1093/brain/aww249. Epub 2016 Oct 25. Brain. 2016. PMID: 27797808 Free PMC article.
[Smallpox].
Kurashige T, Morisawa Y, Fujieda M. Kurashige T, et al. Ryoikibetsu Shokogun Shirizu. 1999;(24 Pt 2):141-4. Ryoikibetsu Shokogun Shirizu. 1999. PMID: 10201160 Review. Japanese. No abstract available.
Mitochondrial localization of PABPN1 in oculopharyngeal muscular dystrophy.
Doki T, Yamashita S, Wei FY, Hara K, Yamamoto T, Zhang Z, Zhang X, Tawara N, Hino H, Uyama E, Kurashige T, Maruyama H, Tomizawa K, Ando Y. Doki T, et al. Among authors: kurashige t. Lab Invest. 2019 Nov;99(11):1728-1740. doi: 10.1038/s41374-019-0243-8. Epub 2019 Mar 20. Lab Invest. 2019. PMID: 30894671
Optineurin defects cause TDP43-pathology with autophagic vacuolar formation.
Kurashige T, Kuramochi M, Ohsawa R, Yamashita Y, Shioi G, Morino H, Kamada M, Ayaki T, Ito H, Sotomaru Y, Maruyama H, Kawakami H. Kurashige T, et al. Neurobiol Dis. 2021 Jan;148:105215. doi: 10.1016/j.nbd.2020.105215. Epub 2020 Dec 6. Neurobiol Dis. 2021. PMID: 33296728 Free article.
A mutant MATR3 mouse model to explain multisystem proteinopathy.
Zhang X, Yamashita S, Hara K, Doki T, Tawara N, Ikeda T, Misumi Y, Zhang Z, Matsuo Y, Nagai M, Kurashige T, Maruyama H, Ando Y. Zhang X, et al. Among authors: kurashige t. J Pathol. 2019 Oct;249(2):182-192. doi: 10.1002/path.5289. Epub 2019 Jun 18. J Pathol. 2019. PMID: 31056746
Biallelic mutation of HSD17B4 induces middle age-onset spinocerebellar ataxia.
Matsuda Y, Morino H, Miyamoto R, Kurashige T, Kume K, Mizuno N, Kanaya Y, Tada Y, Ohsawa R, Yokota K, Shimozawa N, Maruyama H, Kawakami H. Matsuda Y, et al. Among authors: kurashige t. Neurol Genet. 2020 Jan 16;6(1):e396. doi: 10.1212/NXG.0000000000000396. eCollection 2020 Feb. Neurol Genet. 2020. PMID: 32042923 Free PMC article.
216 results
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