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3. CARD15/NOD2 gene variants are associated with familially occurring and complicated forms of Crohn's disease. Heliö T; Halme L; Lappalainen M; Fodstad H; Paavola-Sakki P; Turunen U; Färkkilä M; Krusius T; Kontula K Gut; 2003 Apr; 52(4):558-62. PubMed ID: 12631669 [TBL] [Abstract][Full Text] [Related]
4. 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; 71(6):538-47. PubMed ID: 18489434 [TBL] [Abstract][Full Text] [Related]
5. 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; 16(14):1753-8. PubMed ID: 20380008 [TBL] [Abstract][Full Text] [Related]
6. Genotype-phenotype analysis in childhood-onset Crohn's disease: NOD2/CARD15 variants consistently predict phenotypic characteristics of severe disease. Russell RK; Drummond HE; Nimmo EE; Anderson N; Smith L; Wilson DC; Gillett PM; McGrogan P; Hassan K; Weaver LT; Bisset M; Mahdi G; Satsangi J Inflamm Bowel Dis; 2005 Nov; 11(11):955-64. PubMed ID: 16239840 [TBL] [Abstract][Full Text] [Related]
7. [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; Orv Hetil; 2004 Jul; 145(27):1403-11. PubMed ID: 15320482 [TBL] [Abstract][Full Text] [Related]
8. 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; 16(11):1177-82. PubMed ID: 15489579 [TBL] [Abstract][Full Text] [Related]
9. Crohn's disease patients carrying Nod2/CARD15 gene variants have an increased and early need for first surgery due to stricturing disease and higher rate of surgical recurrence. Alvarez-Lobos M; Arostegui JI; Sans M; Tassies D; Plaza S; Delgado S; Lacy AM; Pique JM; Yagüe J; Panés J Ann Surg; 2005 Nov; 242(5):693-700. PubMed ID: 16244543 [TBL] [Abstract][Full Text] [Related]
10. Association of polymorphisms in the interleukin-18 gene in patients with Crohn's disease depending on the CARD15/NOD2 genotype. Glas J; Török HP; Tonenchi L; Kapser J; Schiemann U; Müller-Myhsok B; Folwaczny M; Folwaczny C Inflamm Bowel Dis; 2005 Dec; 11(12):1031-7. PubMed ID: 16306764 [TBL] [Abstract][Full Text] [Related]
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12. CARD15 gene mutations and risk for early surgery in pediatric-onset Crohn's disease. Kugathasan S; Collins N; Maresso K; Hoffmann RG; Stephens M; Werlin SL; Rudolph C; Broeckel U Clin Gastroenterol Hepatol; 2004 Nov; 2(11):1003-9. PubMed ID: 15551253 [TBL] [Abstract][Full Text] [Related]
13. 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; 41(6):700-5. PubMed ID: 16716969 [TBL] [Abstract][Full Text] [Related]
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20. 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; 11(5):681-5. PubMed ID: 15655821 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]