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

Year Number of Results
1980 1
1981 4
1982 2
1983 1
1985 1
1987 1
1992 2
1993 2
1995 3
1997 2
1998 2
1999 6
2000 1
2002 1
2003 3
2004 1
2005 1
2006 5
2007 3
2008 1
2009 2
2010 1
2011 2
2012 1
2013 3
2014 1
2015 2
2016 1
2022 0
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Search Results

52 results
Results by year
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Page 1
High-throughput genomic analysis in Waldenström's macroglobulinemia.
Poulain S, Braggio E, Roumier C, Aijjou R, Broucqsault N, Galiègue-Zouitina S, Manier S, Soenen V, Nibourel O, Duthilleul P, Fonseca R, Leleu X. Poulain S, et al. Among authors: duthilleul p. Clin Lymphoma Myeloma Leuk. 2011 Feb;11(1):106-8. doi: 10.3816/CLML.2011.n.021. Clin Lymphoma Myeloma Leuk. 2011. PMID: 21454205 Review.
Serological markers in inflammatory bowel diseases.
Reumaux D, Sendid B, Poulain D, Duthilleul P, Dewit O, Colombel JF. Reumaux D, et al. Among authors: duthilleul p. Best Pract Res Clin Gastroenterol. 2003 Feb;17(1):19-35. doi: 10.1053/bega.2002.0347. Best Pract Res Clin Gastroenterol. 2003. PMID: 12617880 Review.
MYD88 L265P mutation in Waldenstrom macroglobulinemia.
Poulain S, Roumier C, Decambron A, Renneville A, Herbaux C, Bertrand E, Tricot S, Daudignon A, Galiègue-Zouitina S, Soenen V, Theisen O, Grardel N, Nibourel O, Roche-Lestienne C, Quesnel B, Duthilleul P, Preudhomme C, Leleu X. Poulain S, et al. Among authors: duthilleul p. Blood. 2013 May 30;121(22):4504-11. doi: 10.1182/blood-2012-06-436329. Epub 2013 Mar 26. Blood. 2013. PMID: 23532735 Free article.
Genomic Landscape of CXCR4 Mutations in Waldenström Macroglobulinemia.
Poulain S, Roumier C, Venet-Caillault A, Figeac M, Herbaux C, Marot G, Doye E, Bertrand E, Geffroy S, Lepretre F, Nibourel O, Decambron A, Boyle EM, Renneville A, Tricot S, Daudignon A, Quesnel B, Duthilleul P, Preudhomme C, Leleu X. Poulain S, et al. Among authors: duthilleul p. Clin Cancer Res. 2016 Mar 15;22(6):1480-8. doi: 10.1158/1078-0432.CCR-15-0646. Epub 2015 Oct 21. Clin Cancer Res. 2016. PMID: 26490317 Free article.
MYD88 L265P mutation contributes to the diagnosis of Bing Neel syndrome.
Poulain S, Boyle EM, Roumier C, Demarquette H, Wemeau M, Geffroy S, Herbaux C, Bertrand E, Hivert B, Terriou L, Verrier A, Pollet JP, Maurage CA, Onraed B, Morschhauser F, Quesnel B, Duthilleul P, Preudhomme C, Leleu X. Poulain S, et al. Among authors: duthilleul p. Br J Haematol. 2014 Nov;167(4):506-13. doi: 10.1111/bjh.13078. Epub 2014 Aug 27. Br J Haematol. 2014. PMID: 25160558 Clinical Trial.
52 results