These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


182 related items for PubMed ID: 15843082

  • 1. A functional interleukin-10 mutation in Dutch patients with Crohn's disease.
    van der Linde K, Boor PP, van Bodegraven AA, de Jong DJ, Crusius JB, Naber TH, Kuipers EJ, Wilson JH, de Rooij FW.
    Dig Liver Dis; 2005 May; 37(5):330-5. PubMed ID: 15843082
    [Abstract] [Full Text] [Related]

  • 2. CARD15 mutations in Dutch familial and sporadic inflammatory bowel disease and an overview of European studies.
    van der Linde K, Boor PP, Houwing-Duistermaat JJ, Crusius BJ, Wilson PJ, Kuipers EJ, de Rooij FW.
    Eur J Gastroenterol Hepatol; 2007 Jun; 19(6):449-59. PubMed ID: 17489054
    [Abstract] [Full Text] [Related]

  • 3. [NOD2/CARD15 mutations and genotype-phenotype correlations in patients with Crohn's disease. Hungarian multicenter study].
    Lakatos L, Lakatos PL, Willheim-Polli C, Reinisch W, Ferenci P, Tulassay Z, Molnár T, Kovács A, Papp J, Szalay F, Hungarian IBD Study Group.
    Orv Hetil; 2004 Jul 04; 145(27):1403-11. PubMed ID: 15320482
    [Abstract] [Full Text] [Related]

  • 4. CARD15 mutations in patients with Crohn's disease in a homogeneous Spanish population.
    Núñez C, Barreiro M, Domínguez-Muñoz JE, Lorenzo A, Zapata C, Peña AS.
    Am J Gastroenterol; 2004 Mar 04; 99(3):450-6. PubMed ID: 15056084
    [Abstract] [Full Text] [Related]

  • 5. Genetic basis for increased intestinal permeability in families with Crohn's disease: role of CARD15 3020insC mutation?
    Buhner S, Buning C, Genschel J, Kling K, Herrmann D, Dignass A, Kuechler I, Krueger S, Schmidt HH, Lochs H.
    Gut; 2006 Mar 04; 55(3):342-7. PubMed ID: 16000642
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. A Gly15Arg mutation in the interleukin-10 gene reduces secretion of interleukin-10 in Crohn disease.
    van der Linde K, Boor PP, Sandkuijl LA, Meijssen MA, Savelkoul HF, Wilson JH, de Rooij FW.
    Scand J Gastroenterol; 2003 Jun 04; 38(6):611-7. PubMed ID: 12825869
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Homozygosity for the CARD15 frameshift mutation 1007fs is predictive of early onset of Crohn's disease with ileal stenosis, entero-enteral fistulas, and frequent need for surgical intervention with high risk of re-stenosis.
    Seiderer J, Schnitzler F, Brand S, Staudinger T, Pfennig S, Herrmann K, Hofbauer K, Dambacher J, Tillack C, Sackmann M, Göke B, Lohse P, Ochsenkühn T.
    Scand J Gastroenterol; 2006 Dec 04; 41(12):1421-32. PubMed ID: 17101573
    [Abstract] [Full Text] [Related]

  • 15. Association of interleukin-1 receptor-associated kinase M (IRAK-M) and inflammatory bowel diseases.
    Weersma RK, Oostenbrug LE, Nolte IM, Van Der Steege G, Oosterom E, Van Dullemen HM, Kleibeuker JH, Dijkstra G.
    Scand J Gastroenterol; 2007 Jul 04; 42(7):827-33. PubMed ID: 17558906
    [Abstract] [Full Text] [Related]

  • 16. NOD1 gene E266K polymorphism is associated with disease susceptibility but not with disease phenotype or NOD2/CARD15 in Hungarian patients with Crohn's disease.
    Molnar T, Hofner P, Nagy F, Lakatos PL, Fischer S, Lakatos L, Kovacs A, Altorjay I, Papp M, Palatka K, Demeter P, Tulassay Z, Nyari T, Miheller P, Papp J, Mandi Y, Lonovics J, Hungarian IBD Study Group.
    Dig Liver Dis; 2007 Dec 04; 39(12):1064-70. PubMed ID: 17964870
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Three common CARD15 mutations are not responsible for the pathogenesis of Crohn's disease in Iranians.
    Teimoori-Toolabi L, Vahedi H, Mollahajian H, Kamali E, Hajizadeh-Sikaroodi S, Zeinali S, Tabrizian T, Olfati G, Rashtak S, Malekzadeh F, Ghoddosi A, Malekzadeh R.
    Hepatogastroenterology; 2010 Dec 04; 57(98):275-82. PubMed ID: 20583427
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Molecular prediction of disease risk and severity in a large Dutch Crohn's disease cohort.
    Weersma RK, Stokkers PC, van Bodegraven AA, van Hogezand RA, Verspaget HW, de Jong DJ, van der Woude CJ, Oldenburg B, Linskens RK, Festen EA, van der Steege G, Hommes DW, Crusius JB, Wijmenga C, Nolte IM, Dijkstra G, Dutch Initiative on Crohn and Colitis (ICC).
    Gut; 2009 Mar 04; 58(3):388-95. PubMed ID: 18824555
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 10.