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

Year Number of Results
1961 1
1965 1
1969 4
1971 7
1972 1
1974 3
1983 2
1986 1
1987 1
1988 1
1990 3
1991 2
1992 6
1993 5
1994 1
1996 1
1997 1
1998 2
2000 4
2001 3
2002 4
2003 5
2004 5
2005 2
2006 4
2007 10
2008 4
2009 6
2010 8
2011 6
2012 15
2013 18
2014 14
2015 13
2016 18
2017 21
2018 21
2019 13
2020 10
2021 20
2022 27
2023 13

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270 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: hashiguchi a. Brain. 2016 Dec;139(Pt 12):3170-3186. doi: 10.1093/brain/aww249. Epub 2016 Oct 25. Brain. 2016. PMID: 27797808 Free PMC article.
Long-read sequencing identifies GGC repeat expansions in NOTCH2NLC associated with neuronal intranuclear inclusion disease.
Sone J, Mitsuhashi S, Fujita A, Mizuguchi T, Hamanaka K, Mori K, Koike H, Hashiguchi A, Takashima H, Sugiyama H, Kohno Y, Takiyama Y, Maeda K, Doi H, Koyano S, Takeuchi H, Kawamoto M, Kohara N, Ando T, Ieda T, Kita Y, Kokubun N, Tsuboi Y, Katoh K, Kino Y, Katsuno M, Iwasaki Y, Yoshida M, Tanaka F, Suzuki IK, Frith MC, Matsumoto N, Sobue G. Sone J, et al. Among authors: hashiguchi a. Nat Genet. 2019 Aug;51(8):1215-1221. doi: 10.1038/s41588-019-0459-y. Epub 2019 Jul 22. Nat Genet. 2019. PMID: 31332381
A Novel PRPS1 Mutation in a Japanese Patient with CMTX5.
Shirakawa S, Murakami T, Hashiguchi A, Takashima H, Hasegawa H, Ichida K, Sunada Y. Shirakawa S, et al. Among authors: hashiguchi a. Intern Med. 2022 Jun 1;61(11):1749-1751. doi: 10.2169/internalmedicine.8029-21. Epub 2021 Nov 20. Intern Med. 2022. PMID: 34803094 Free PMC article.
A grading system that predicts the risk of dialysis induction in IgA nephropathy patients based on the combination of the clinical and histological severity.
Okonogi H, Kawamura T, Joh K, Koike K, Miyazaki Y, Ogura M, Tsuboi N, Hirano K, Matsushima M, Yokoo T, Horikoshi S, Suzuki Y, Yasuda T, Shirai S, Shibata T, Hattori M, Akioka Y, Katafuchi R, Hashiguchi A, Hisano S, Shimizu A, Kimura K, Maruyama S, Matsuo S, Tomino Y; Special IgA Nephropathy Study Group. Okonogi H, et al. Among authors: hashiguchi a. Clin Exp Nephrol. 2019 Jan;23(1):16-25. doi: 10.1007/s10157-018-1657-0. Epub 2018 Oct 26. Clin Exp Nephrol. 2019. PMID: 30367317 Free PMC article. Review.
Minimal Change Disease Associated With Durvalumab.
Toda MG, Fujii K, Kato A, Yoshifuji A, Komatsu M, Amino Y, Kitazono S, Hashiguchi A, Ryuzaki M. Toda MG, et al. Among authors: hashiguchi a. Kidney Int Rep. 2021 Sep 1;6(10):2733-2734. doi: 10.1016/j.ekir.2021.08.021. eCollection 2021 Oct. Kidney Int Rep. 2021. PMID: 34622115 Free PMC article. No abstract available.
[Paraneoplastic myositis].
Hashiguchi A, Higuchi I. Hashiguchi A, et al. Nihon Rinsho. 2015 Sep;73 Suppl 7:788-92. Nihon Rinsho. 2015. PMID: 26480795 Japanese. No abstract available.
Fabry disease associated with multiple myeloma: a case report.
Adachi K, Tokuyama H, Oshima Y, Itoh T, Hashiguchi A, Yamakawa H, Togawa T, Sakuraba H, Wakino S, Itoh H. Adachi K, et al. Among authors: hashiguchi a. CEN Case Rep. 2022 Feb;11(1):146-153. doi: 10.1007/s13730-021-00613-x. Epub 2021 Sep 16. CEN Case Rep. 2022. PMID: 34529243 Free PMC article.
270 results