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PUBMED FOR HANDHELDS

Journal Abstract Search


608 related items for PubMed ID: 12631669

  • 21. Frequency of NOD2/CARD15 variants in both sporadic and familial cases of Crohn's disease across Italy. An Italian Group for Inflammatory Bowel Disease Study.
    Annese V, Palmieri O, Latiano A, Ardizzone S, Castiglione F, Cottone M, D'Incà R, Gionchetti P, Papi C, Riegler G, Vecchi M, Andriulli A, Italian Group for Inflammatory Bowel Disease.
    Dig Liver Dis; 2004 Feb; 36(2):121-4. PubMed ID: 15002819
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  • 23. Novel CARD15/NOD2 mutations in Finnish patients with Crohn's disease and their relation to phenotypic variation in vitro and in vivo.
    Lappalainen M, Paavola-Sakki P, Halme L, Turunen U, Färkkilä M, Repo H, Kontula K.
    Inflamm Bowel Dis; 2008 Feb; 14(2):176-85. PubMed ID: 17941079
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  • 24. Transmission of CARD15 (NOD2) variants within families of patients with inflammatory bowel disease.
    Esters N, Pierik M, van Steen K, Vermeire S, Claessens G, Joossens S, Vlietinck R, Rutgeerts P.
    Am J Gastroenterol; 2004 Feb; 99(2):299-305. PubMed ID: 15046221
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  • 27. CARD15 genotype-phenotype relationships in a small inflammatory bowel disease population with severe disease affection status.
    Crawford NP, Colliver DW, Eichenberger MR, Funke AA, Kolodko V, Cobbs GA, Petras RE, Galandiuk S.
    Dig Dis Sci; 2007 Oct; 52(10):2716-24. PubMed ID: 17404888
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  • 29. NOD2/CARD15 variants are associated with lower weight at diagnosis in children with Crohn's disease.
    Tomer G, Ceballos C, Concepcion E, Benkov KJ.
    Am J Gastroenterol; 2003 Nov; 98(11):2479-84. PubMed ID: 14638352
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  • 30. Development of rheumatoid arthritis is not associated with two polymorphisms in the Crohn's disease gene CARD15.
    Steer S, Fisher SA, Fife M, Cuthbert A, Newton J, Wordsworth P, Lewis CM, Mathew CG, Lanchbury JS.
    Rheumatology (Oxford); 2003 Feb; 42(2):304-7. PubMed ID: 12595627
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  • 32. Genetic association and phenotypic correlation of TLR4 but not NOD2 variants with Tunisian inflammatory bowel disease.
    Feki S, Bouzid D, Abida O, Chtourou L, Elloumi N, Toumi A, Hachicha H, Amouri A, Tahri N, Masmoudi H.
    J Dig Dis; 2017 Nov; 18(11):625-633. PubMed ID: 29055077
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  • 33. Relationship between CARD15, SLC22A4/5, and DLG5 polymorphisms and early-onset inflammatory bowel diseases: an Italian multicentric study.
    Ferraris A, Torres B, Knafelz D, Barabino A, Lionetti P, de Angelis GL, Iacono G, Papadatou B, D'Amato G, Di Ciommo V, Dallapiccola B, Castro M.
    Inflamm Bowel Dis; 2006 May; 12(5):355-61. PubMed ID: 16670523
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  • 34. NOD2/CARD15 gene mutations in North Algerian patients with inflammatory bowel disease.
    Boukercha A, Mesbah-Amroun H, Bouzidi A, Saoula H, Nakkemouche M, Roy M, Hugot JP, Touil-Boukoffa C.
    World J Gastroenterol; 2015 Jul 07; 21(25):7786-94. PubMed ID: 26167078
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  • 35. Toll-like receptor 4 and NOD2/CARD15 mutations in Hungarian patients with Crohn's disease: phenotype-genotype correlations.
    Lakatos PL, Lakatos L, Szalay F, Willheim-Polli C, Osterreicher C, Tulassay Z, Molnar T, Reinisch W, Papp J, Mozsik G, Ferenci P, Hungarian IBD Study Group.
    World J Gastroenterol; 2005 Mar 14; 11(10):1489-95. PubMed ID: 15770725
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  • 37. Association of chronic non-bacterial osteomyelitis with Crohn's disease but not with CARD15 gene variants.
    Morbach H, Dick A, Beck C, Stenzel M, Müller-Hermelink HK, Raab P, Girschick HJ.
    Rheumatol Int; 2010 Mar 14; 30(5):617-21. PubMed ID: 19579029
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  • 39. NOD2/CARD15, NOD1/CARD4, and ICAM-1 gene polymorphisms in Turkish patients with inflammatory bowel disease.
    Ozen SC, Dagli U, Kiliç MY, Törüner M, Celik Y, Ozkan M, Soykan I, Cetinkaya H, Ulker A, Ozden A, Bozdayi AM.
    J Gastroenterol; 2006 Apr 14; 41(4):304-10. PubMed ID: 16741608
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  • 40. CARD15 gene polymorphisms in Serbian patients with Crohn's disease: genotype-phenotype analysis.
    Protic MB, Pavlovic ST, Bojic DZ, Krstic MN, Radojicic ZA, Tarabar DK, Stevanovic AZ, Karan Djurasevic TZ, Godjevac MV, Svorcan PV, Dapcevic BD, Jojic NZ.
    Eur J Gastroenterol Hepatol; 2008 Oct 14; 20(10):978-84. PubMed ID: 18787464
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