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

Year Number of Results
1998 2
1999 4
2000 4
2001 5
2002 3
2004 1
2005 4
2006 3
2007 2
2008 5
2009 6
2010 2
2011 3
2012 4
2013 5
2014 4
2015 5
2016 6
2017 6
2018 7
2019 4
2020 7
2021 3
2024 0

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Similar articles for PMID: 19178939

83 results

Results by year

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Page 1
Novel presentation of Omenn syndrome in association with aniridia.
Sheehan WJ, Delmonte OM, Miller DT, Roberts AE, Bonilla FA, Morra M, Giliani S, Pai SY, Notarangelo LD, Oettgen HC. Sheehan WJ, et al. J Allergy Clin Immunol. 2009 Apr;123(4):966-9. doi: 10.1016/j.jaci.2008.12.007. J Allergy Clin Immunol. 2009. PMID: 19178939 Free PMC article.
Omenn syndrome with mutation in RAG1 gene.
Jaouad IC, Ouldim K, Ali Ou Alla S, Kriouile Y, Villa A, Sefiani A. Jaouad IC, et al. Indian J Pediatr. 2008 Sep;75(9):944-6. doi: 10.1007/s12098-008-0197-0. Epub 2008 Nov 15. Indian J Pediatr. 2008. PMID: 19011808
[Omenn Syndrome and DNA recombination defects].
Yachie A. Yachie A. Nihon Rinsho Meneki Gakkai Kaishi. 2017;40(3):179-189. doi: 10.2177/jsci.40.179. Nihon Rinsho Meneki Gakkai Kaishi. 2017. PMID: 28747605 Free article. Review. Japanese.
Omenn syndrome due to mutation of the RAG2 gene.
Ktiouet S, Bertrand Y, Rival-Tringali AL, Kanitakis J, Malcus C, Poitevin F, Picard C, Claudy A, Faure M. Ktiouet S, et al. J Eur Acad Dermatol Venereol. 2009 Dec;23(12):1449-51. doi: 10.1111/j.1468-3083.2009.03232.x. Epub 2009 Mar 12. J Eur Acad Dermatol Venereol. 2009. PMID: 19470080 No abstract available.
Analysis of mutations and recombination activity in RAG-deficient patients.
Asai E, Wada T, Sakakibara Y, Toga A, Toma T, Shimizu T, Nampoothiri S, Imai K, Nonoyama S, Morio T, Muramatsu H, Kamachi Y, Ohara O, Yachie A. Asai E, et al. Clin Immunol. 2011 Feb;138(2):172-7. doi: 10.1016/j.clim.2010.11.005. Epub 2010 Dec 4. Clin Immunol. 2011. PMID: 21131235
83 results