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

Year Number of Results
1993 1
1994 1
1995 1
1996 4
1997 1
1998 3
2001 2
2003 1
2004 2
2005 2
2006 1
2007 3
2009 4
2011 3
2012 1
2013 4
2014 4
2015 3
2016 2
2017 2
2018 2
2019 2
2022 0
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Search Results

43 results
Results by year
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Page 1
Aggressive angiomyxoma.
Gay F, Champigneulle J, Tortuyaux JM, Cuny T, Régent D, Laurent-Croisé V. Gay F, et al. Among authors: champigneulle j. Diagn Interv Imaging. 2013 Jun;94(6):657-61. doi: 10.1016/j.diii.2013.01.009. Epub 2013 Feb 26. Diagn Interv Imaging. 2013. PMID: 23453353 Free article. No abstract available.
[Formaldehyde fixation in the third millennium].
Plénat F, Antunes L, Haller T, Piet-Ounnoughene M, Klein-Monhoven N, Champigneulle J, Chenal P, Bland V, Garcia-Pimenta F, Labouyrie E. Plénat F, et al. Among authors: champigneulle j. Ann Pathol. 2001 Feb;21(1):29-47. Ann Pathol. 2001. PMID: 11223558 Review. French.
Clear cell rhabdomyosarcoma.
Boman F, Champigneulle J, Schmitt C, Beurey P, Floquet J, Boccon-Gibod L. Boman F, et al. Among authors: champigneulle j. Pediatr Pathol Lab Med. 1996 Nov-Dec;16(6):951-9. doi: 10.1080/15513819609168718. Pediatr Pathol Lab Med. 1996. PMID: 9025893
Pigmented villonodular synovitis of the wrist in childhood.
Hoeffel JC, Mainard L, Champigneulle J, Claudon M. Hoeffel JC, et al. Among authors: champigneulle j. Clin Pediatr (Phila). 1997 Jul;36(7):423-6. doi: 10.1177/000992289703600709. Clin Pediatr (Phila). 1997. PMID: 9241482 Review. No abstract available.
Contribution of de novo and mosaic TP53 mutations to Li-Fraumeni syndrome.
Renaux-Petel M, Charbonnier F, Théry JC, Fermey P, Lienard G, Bou J, Coutant S, Vezain M, Kasper E, Fourneaux S, Manase S, Blanluet M, Leheup B, Mansuy L, Champigneulle J, Chappé C, Longy M, Sévenet N, Paillerets BB, Guerrini-Rousseau L, Brugières L, Caron O, Sabourin JC, Tournier I, Baert-Desurmont S, Frébourg T, Bougeard G. Renaux-Petel M, et al. Among authors: champigneulle j. J Med Genet. 2018 Mar;55(3):173-180. doi: 10.1136/jmedgenet-2017-104976. Epub 2017 Oct 25. J Med Genet. 2018. PMID: 29070607
DNA methylation heterogeneity defines a disease spectrum in Ewing sarcoma.
Sheffield NC, Pierron G, Klughammer J, Datlinger P, Schönegger A, Schuster M, Hadler J, Surdez D, Guillemot D, Lapouble E, Freneaux P, Champigneulle J, Bouvier R, Walder D, Ambros IM, Hutter C, Sorz E, Amaral AT, de Álava E, Schallmoser K, Strunk D, Rinner B, Liegl-Atzwanger B, Huppertz B, Leithner A, de Pinieux G, Terrier P, Laurence V, Michon J, Ladenstein R, Holter W, Windhager R, Dirksen U, Ambros PF, Delattre O, Kovar H, Bock C, Tomazou EM. Sheffield NC, et al. Among authors: champigneulle j. Nat Med. 2017 Mar;23(3):386-395. doi: 10.1038/nm.4273. Epub 2017 Jan 30. Nat Med. 2017. PMID: 28134926 Free PMC article.
LMX1B mutations cause hereditary FSGS without extrarenal involvement.
Boyer O, Woerner S, Yang F, Oakeley EJ, Linghu B, Gribouval O, Tête MJ, Duca JS, Klickstein L, Damask AJ, Szustakowski JD, Heibel F, Matignon M, Baudouin V, Chantrel F, Champigneulle J, Martin L, Nitschké P, Gubler MC, Johnson KJ, Chibout SD, Antignac C. Boyer O, et al. Among authors: champigneulle j. J Am Soc Nephrol. 2013 Jul;24(8):1216-22. doi: 10.1681/ASN.2013020171. Epub 2013 May 16. J Am Soc Nephrol. 2013. PMID: 23687361 Free PMC article.
43 results