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

Year Number of Results
1965 1
1969 1
1972 2
1973 1
1974 2
1976 3
1977 2
1978 1
1979 3
1980 1
1981 3
1984 2
1986 1
1987 1
1991 4
1992 3
1993 3
1994 3
1995 10
1996 2
1997 3
1998 7
1999 7
2000 10
2001 4
2002 3
2003 6
2004 6
2005 11
2006 22
2007 20
2008 22
2009 20
2010 19
2011 21
2012 19
2013 15
2014 20
2015 19
2016 23
2017 22
2018 35
2019 28
2020 20
2021 26
2022 25
Text availability
Article attribute
Article type
Publication date

Search Results

426 results
Results by year
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Page 1
Autosomal Dominant Nocturnal Frontal Lobe Epilepsy.
Kurahashi H, Hirose S. Kurahashi H, et al. 2002 May 16 [updated 2018 Mar 15]. 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. 2002 May 16 [updated 2018 Mar 15]. 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: 20301348 Free Books & Documents. Review.
Preimplantation genetic testing for aneuploidy: a comparison of live birth rates in patients with recurrent pregnancy loss due to embryonic aneuploidy or recurrent implantation failure.
Sato T, Sugiura-Ogasawara M, Ozawa F, Yamamoto T, Kato T, Kurahashi H, Kuroda T, Aoyama N, Kato K, Kobayashi R, Fukuda A, Utsunomiya T, Kuwahara A, Saito H, Takeshita T, Irahara M. Sato T, et al. Among authors: kurahashi h. Hum Reprod. 2019 Dec 1;34(12):2340-2348. doi: 10.1093/humrep/dez229. Hum Reprod. 2019. PMID: 31811307
Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy.
Bonora E, Chakrabarty S, Kellaris G, Tsutsumi M, Bianco F, Bergamini C, Ullah F, Isidori F, Liparulo I, Diquigiovanni C, Masin L, Rizzardi N, Cratere MG, Boschetti E, Papa V, Maresca A, Cenacchi G, Casadio R, Martelli P, Matera I, Ceccherini I, Fato R, Raiola G, Arrigo S, Signa S, Sementa AR, Severino M, Striano P, Fiorillo C, Goto T, Uchino S, Oyazato Y, Nakamura H, Mishra SK, Yeh YS, Kato T, Nozu K, Tanboon J, Morioka I, Nishino I, Toda T, Goto YI, Ohtake A, Kosaki K, Yamaguchi Y, Nonaka I, Iijima K, Mimaki M, Kurahashi H, Raams A, MacInnes A, Alders M, Engelen M, Linthorst G, de Koning T, den Dunnen W, Dijkstra G, van Spaendonck K, van Gent DC, Aronica EM, Picco P, Carelli V, Seri M, Katsanis N, Duijkers FAM, Taniguchi-Ikeda M, De Giorgio R. Bonora E, et al. Among authors: kurahashi h. Brain. 2021 Jun 22;144(5):1451-1466. doi: 10.1093/brain/awab056. Brain. 2021. PMID: 33855352 Free article.
Fukutin and alpha-dystroglycanopathies.
Toda T, Chiyonobu T, Xiong H, Tachikawa M, Kobayashi K, Manya H, Takeda S, Taniguchi M, Kurahashi H, Endo T. Toda T, et al. Among authors: kurahashi h. Acta Myol. 2005 Oct;24(2):60-3. Acta Myol. 2005. PMID: 16550916 Review.
HPeV3-associated acute encephalitis/encephalopathy among Japanese infants.
Abe Y, Ohno T, Matsumoto H, Daimon Y, Kurahashi H, Takayama R, Sakaguchi Y, Tanabe S, Tanaka F, Miyamoto Y, Kawano A, Yamanouchi H. Abe Y, et al. Among authors: kurahashi h. Brain Dev. 2021 Apr;43(4):528-537. doi: 10.1016/j.braindev.2020.12.010. Epub 2021 Jan 8. Brain Dev. 2021. PMID: 33423809
Clinical spectrum of SCN2A mutations.
Shi X, Yasumoto S, Kurahashi H, Nakagawa E, Fukasawa T, Uchiya S, Hirose S. Shi X, et al. Among authors: kurahashi h. Brain Dev. 2012 Aug;34(7):541-5. doi: 10.1016/j.braindev.2011.09.016. Epub 2011 Oct 24. Brain Dev. 2012. PMID: 22029951 Review.
Chromosomal translocations and palindromic AT-rich repeats.
Kato T, Kurahashi H, Emanuel BS. Kato T, et al. Among authors: kurahashi h. Curr Opin Genet Dev. 2012 Jun;22(3):221-8. doi: 10.1016/j.gde.2012.02.004. Epub 2012 Mar 6. Curr Opin Genet Dev. 2012. PMID: 22402448 Free PMC article. Review.
426 results