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

Year Number of Results
1970 1
1978 2
1983 1
1984 2
1988 3
1989 1
1990 1
1991 3
1996 2
1997 3
1998 1
1999 3
2000 4
2002 2
2003 1
2005 4
2006 2
2007 3
2008 1
2009 2
2010 4
2011 1
2012 3
2013 3
2014 3
2015 1
2016 1
2017 1
2018 1
2022 0
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58 results
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Page 1
Hairy cell leukemia-variant without typical morphology and with near-tetraploid DNA content.
Azoulay D, Sonkin V, Akria L, Rozano Gorelick A, Trakhtenbrot L, Hershkovitz D, Shaoul E, Rozen S, Dementiev E, Cohen HI, Suriu C, Braester A. Azoulay D, et al. Among authors: sonkin v. Cytometry B Clin Cytom. 2018 Jan;94(1):169-171. doi: 10.1002/cyto.b.21503. Epub 2017 Feb 6. Cytometry B Clin Cytom. 2018. PMID: 27997757 Free article. No abstract available.
A founder mutation in Vps37A causes autosomal recessive complex hereditary spastic paraparesis.
Zivony-Elboum Y, Westbroek W, Kfir N, Savitzki D, Shoval Y, Bloom A, Rod R, Khayat M, Gross B, Samri W, Cohen H, Sonkin V, Freidman T, Geiger D, Fattal-Valevski A, Anikster Y, Waters AM, Kleta R, Falik-Zaccai TC. Zivony-Elboum Y, et al. Among authors: sonkin v. J Med Genet. 2012 Jul;49(7):462-72. doi: 10.1136/jmedgenet-2012-100742. Epub 2012 Jun 20. J Med Genet. 2012. PMID: 22717650
Growth variation, final height and secular trend. Proceedings of the 17th Aschauer Soiree, 7th November 2009.
Hermanussen M, Godina E, Rühli FJ, Blaha P, Boldsen JL, van Buuren S, MacIntyre M, Assmann C, Ghosh A, de Stefano GF, Sonkin VD, Tresguerres JA, Meigen C, Scheffler C, Geiger C, Lieberman LS. Hermanussen M, et al. Among authors: sonkin vd. Homo. 2010 Aug;61(4):277-84. doi: 10.1016/j.jchb.2010.06.001. Epub 2010 Jul 13. Homo. 2010. PMID: 20630526 Free article.
58 results