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

Year Number of Results
2002 1
2003 2
2005 1
2006 2
2009 2
2010 3
2011 11
2012 7
2013 11
2014 12
2015 9
2016 12
2017 7
2018 12
2019 8
2020 11
2021 9
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102 results
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Showing results for sarig o[au]
Your search for Sanig O[au] retrieved no results
Variant PADI3 in Central Centrifugal Cicatricial Alopecia.
Malki L, Sarig O, Romano MT, Méchin MC, Peled A, Pavlovsky M, Warshauer E, Samuelov L, Uwakwe L, Briskin V, Mohamad J, Gat A, Isakov O, Rabinowitz T, Shomron N, Adir N, Simon M, McMichael A, Dlova NC, Betz RC, Sprecher E. Malki L, et al. Among authors: sarig o. N Engl J Med. 2019 Feb 28;380(9):833-841. doi: 10.1056/NEJMoa1816614. Epub 2019 Feb 13. N Engl J Med. 2019. PMID: 30763140
The Genetics of Pemphigus Vulgaris.
Vodo D, Sarig O, Sprecher E. Vodo D, et al. Among authors: sarig o. Front Med (Lausanne). 2018 Aug 14;5:226. doi: 10.3389/fmed.2018.00226. eCollection 2018. Front Med (Lausanne). 2018. PMID: 30155467 Free PMC article. Review.
Kaplan Y, Sarig O, Rabinowitz T, Mohamad J, Shomron N, Sprecher E, Goldberg I. Kaplan Y, et al. Among authors: sarig o. Harefuah. 2020 Jan;159(1):25-28. Harefuah. 2020. PMID: 31930803 Hebrew.
Molecular epidemiology of pachyonychia congenita in the Israeli population.
Pavlovsky M, Peled A, Samuelov L, Malki L, Malovitski K, Assaf S, Mohamad J, Meijers O, Eskin-Schwartz M, Sarig O, Sprecher E. Pavlovsky M, et al. Among authors: sarig o. Clin Exp Dermatol. 2021 Jun;46(4):663-668. doi: 10.1111/ced.14509. Epub 2020 Dec 20. Clin Exp Dermatol. 2021. PMID: 33190296
Loss-of-Function Variants in SERPINA12 Underlie Autosomal Recessive Palmoplantar Keratoderma.
Mohamad J, Sarig O, Malki L, Rabinowitz T, Assaf S, Malovitski K, Shkury E, Mayer T, Vodo D, Peled A, Daniely D, Pavlovsky M, Shomron N, Samuelov L, Sprecher E. Mohamad J, et al. Among authors: sarig o. J Invest Dermatol. 2020 Nov;140(11):2178-2187. doi: 10.1016/j.jid.2020.02.030. Epub 2020 Apr 2. J Invest Dermatol. 2020. PMID: 32247861
[Dupuytren's disease].
Sarig O, Hass A, Weizenbluth M, Oron A. Sarig O, et al. Harefuah. 2014 Jan;153(1):19-21, 65. Harefuah. 2014. PMID: 24605402 Review. Hebrew.
Loss-of-function variants in C3ORF52 result in localized autosomal recessive hypotrichosis.
Malki L, Sarig O, Cesarato N, Mohamad J, Canter T, Assaf S, Pavlovsky M, Vodo D, Anis Y, Bihari O, Malovitski K, Gat A, Thiele H, White BEP, Samuelov L, Nanda A, Paller AS, Betz RC, Sprecher E. Malki L, et al. Among authors: sarig o. Genet Med. 2020 Jul;22(7):1227-1234. doi: 10.1038/s41436-020-0794-5. Epub 2020 Apr 27. Genet Med. 2020. PMID: 32336749 Free PMC article.
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