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Journal Abstract Search

427 related items for PubMed ID: 15539413

  • 1. CARD15 gene polymorphisms in patients with spondyloarthropathies identify a specific phenotype previously related to Crohn's disease.
    Laukens D, Peeters H, Marichal D, Vander Cruyssen B, Mielants H, Elewaut D, Demetter P, Cuvelier C, Van Den Berghe M, Rottiers P, Veys EM, Remaut E, Steidler L, De Keyser F, De Vos M.
    Ann Rheum Dis; 2005 Jun; 64(6):930-5. PubMed ID: 15539413
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  • 2. 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; 99(3):450-6. PubMed ID: 15056084
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  • 6. Mutations in the NOD2/CARD15 gene in Crohn's disease are associated with ileocecal resection and are a risk factor for reoperation.
    Büning C, Genschel J, Bühner S, Krüger S, Kling K, Dignass A, Baier P, Bochow B, Ockenga J, Schmidt HH, Lochs H.
    Aliment Pharmacol Ther; 2004 May 15; 19(10):1073-8. PubMed ID: 15142196
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  • 8. 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 15; 39(12):1064-70. PubMed ID: 17964870
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  • 9. NOD2/CARD15 mutation analysis and genotype-phenotype correlation in Jewish pediatric patients compared with adults with Crohn's disease.
    Weiss B, Shamir R, Bujanover Y, Waterman M, Hartman C, Fradkin A, Berkowitz D, Weintraub I, Eliakim R, Karban A.
    J Pediatr; 2004 Aug 15; 145(2):208-12. PubMed ID: 15289769
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  • 10. Variation at NOD2/CARD15 in familial and sporadic cases of Crohn's disease in the Ashkenazi Jewish population.
    Zhou Z, Lin XY, Akolkar PN, Gulwani-Akolkar B, Levine J, Katz S, Silver J.
    Am J Gastroenterol; 2002 Dec 15; 97(12):3095-101. PubMed ID: 12492195
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  • 11. Variants of CARD15, TNFA and PTPN22 and susceptibility to Crohn's disease in the Czech population: high frequency of the CARD15 1007fs.
    Hradsky O, Lenicek M, Dusatkova P, Bronsky J, Nevoral J, Valtrova V, Kotalova R, Szitanyi P, Petro R, Starzykova V, Bortlik M, Vitek L, Lukas M, Cinek O.
    Tissue Antigens; 2008 Jun 15; 71(6):538-47. PubMed ID: 18489434
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  • 12. NOD2/CARD15 genotype and phenotype differences between Ashkenazi and Sephardic Jews with Crohn's disease.
    Karban A, Waterman M, Panhuysen CI, Pollak RD, Nesher S, Datta L, Weiss B, Suissa A, Shamir R, Brant SR, Eliakim R.
    Am J Gastroenterol; 2004 Jun 15; 99(6):1134-40. PubMed ID: 15180737
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  • 13. Identification of NOD2/CARD15 mutations in Malaysian patients with Crohn's disease.
    Chua KH, Hilmi I, Ng CC, Eng TL, Palaniappan S, Lee WS, Goh KL.
    J Dig Dis; 2009 May 15; 10(2):124-30. PubMed ID: 19426395
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  • 14. Variants of CARD15 are associated with an aggressive clinical course of Crohn's disease--an IG-IBD study.
    Annese V, Lombardi G, Perri F, D'Incà R, Ardizzone S, Riegler G, Giaccari S, Vecchi M, Castiglione F, Gionchetti P, Cocchiara E, Vigneri S, Latiano A, Palmieri O, Andriulli A.
    Am J Gastroenterol; 2005 Jan 15; 100(1):84-92. PubMed ID: 15654786
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  • 15. The V249I polymorphism of the CX3CR1 gene is associated with fibrostenotic disease behavior in patients with Crohn's disease.
    Sabate JM, Ameziane N, Lamoril J, Jouet P, Farmachidi JP, Soulé JC, Harnois F, Sobhani I, Jian R, Deybach JC, de Prost D, Coffin B.
    Eur J Gastroenterol Hepatol; 2008 Aug 15; 20(8):748-55. PubMed ID: 18617779
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  • 16. 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 15; 19(6):449-59. PubMed ID: 17489054
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  • 17. Mutations in CARD15 and smoking confer susceptibility to Crohn's disease in the Danish population.
    Ernst A, Jacobsen B, Østergaard M, Okkels H, Andersen V, Dagiliene E, Pedersen IS, Thorsgaard N, Drewes AM, Krarup HB.
    Scand J Gastroenterol; 2007 Dec 15; 42(12):1445-51. PubMed ID: 17852840
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  • 18. Association of NOD2/CARD15 mutations on Crohn's disease phenotype in an Italian population.
    Bianchi V, Maconi G, Ardizzone S, Colombo E, Ferrara E, Russo A, Tenchini ML, Porro GB.
    Eur J Gastroenterol Hepatol; 2007 Mar 15; 19(3):217-23. PubMed ID: 17301648
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  • 19. 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 15; 55(3):342-7. PubMed ID: 16000642
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  • 20. CARD15 in inflammatory bowel disease and Crohn's disease phenotypes: an association study and pooled analysis.
    Oostenbrug LE, Nolte IM, Oosterom E, van der Steege G, te Meerman GJ, van Dullemen HM, Drenth JP, de Jong DJ, van der Linde K, Jansen PL, Kleibeuker JH.
    Dig Liver Dis; 2006 Nov 15; 38(11):834-45. PubMed ID: 16920047
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