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Journal Abstract Search

608 related items for PubMed ID: 12631669

  • 1.
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  • 2. NOD2/CARD15 gene polymorphisms in Crohn's disease: a genotype- phenotype analysis.
    Heresbach D, Gicquel-Douabin V, Birebent B, D'halluin PN, Heresbach-Le Berre N, Dreano S, Siproudhis L, Dabadie A, Gosselin M, Mosser J, Semana G, Bretagne JF, Yaouanq J.
    Eur J Gastroenterol Hepatol; 2004 Jan; 16(1):55-62. PubMed ID: 15095853
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  • 3. 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; 97(12):3095-101. PubMed ID: 12492195
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  • 5. 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; 100(1):84-92. PubMed ID: 15654786
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  • 8. Analysis of the CARD15 variants R702W, G908R and L1007fs in Italian IBD patients.
    Giachino D, van Duist MM, Regazzoni S, Gregori D, Bardessono M, Salacone P, Scaglione N, Sostegni R, Sapone N, Bresso F, Sambataro A, Gaia E, Pera A, Astegiano M, De Marchi M.
    Eur J Hum Genet; 2004 Mar; 12(3):206-12. PubMed ID: 14747834
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  • 9. Clinical significance of NOD2/CARD15 and Toll-like receptor 4 gene single nucleotide polymorphisms in inflammatory bowel disease.
    Rigoli L, Romano C, Caruso RA, Lo Presti MA, Di Bella C, Procopio V, Lo Giudice G, Amorini M, Costantino G, Sergi MD, Cuppari C, Calabro GE, Gallizzi R, Salpietro CD, Fries W.
    World J Gastroenterol; 2008 Jul 28; 14(28):4454-61. PubMed ID: 18680223
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  • 11. Association between polymorphisms in the Toll-like receptor 4, CD14, and CARD15/NOD2 and inflammatory bowel disease in the Greek population.
    Gazouli M, Mantzaris G, Kotsinas A, Zacharatos P, Papalambros E, Archimandritis A, Ikonomopoulos J, Gorgoulis VG.
    World J Gastroenterol; 2005 Feb 07; 11(5):681-5. PubMed ID: 15655821
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  • 12. [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
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  • 13. 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 04; 145(2):208-12. PubMed ID: 15289769
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  • 14. NOD2/CARD15, ATG16L1 and IL23R gene polymorphisms and childhood-onset of Crohn's disease.
    Gazouli M, Pachoula I, Panayotou I, Mantzaris G, Chrousos G, Anagnou NP, Roma-Giannikou E.
    World J Gastroenterol; 2010 Apr 14; 16(14):1753-8. PubMed ID: 20380008
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  • 15. Association of NOD2/CARD15 variants with Crohn's disease in a Greek population.
    Gazouli M, Zacharatos P, Mantzaris GJ, Barbatis C, Ikonomopoulos I, Archimandritis AJ, Lukas JC, Papalambros E, Gorgoulis V.
    Eur J Gastroenterol Hepatol; 2004 Nov 14; 16(11):1177-82. PubMed ID: 15489579
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  • 17. Contribution of CARD15 variants in determining susceptibility to Crohn's disease in Sweden.
    Törkvist L, Noble CL, Lördal M, Sjöqvist U, Lindforss U, Nimmo ER, Russell RK, Löfberg R, Satsangi J.
    Scand J Gastroenterol; 2006 Jun 14; 41(6):700-5. PubMed ID: 16716969
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  • 18. Common NOD2/CARD15 and TLR4 Polymorphisms Are Associated with Crohn's Disease Phenotypes in Southeastern Brazilians.
    Tolentino YF, Elia PP, Fogaça HS, Carneiro AJ, Zaltman C, Moura-Neto R, Luiz RR, Carvalho Mda G, de Souza HS.
    Dig Dis Sci; 2016 Sep 14; 61(9):2636-47. PubMed ID: 27107867
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  • 19. Frequency of CARD15 polymorphisms in patients with Crohn's disease from Toledo, Spain: genotype-phenotype correlation.
    De Diego C, Alcántara M, Valle J, Pérez-Grueso MJ, Muñoz-Rosas C, Carrobles JM, Martínez-Castro P.
    Genet Test; 2006 Sep 14; 10(3):178-85. PubMed ID: 17020469
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