Similar articles for PMID: 17763471

Year	Number of Results
1947	1
1955	1
1958	1
2001	1
2002	5
2003	14
2004	18
2005	24
2006	15
2007	32
2008	22
2009	10
2010	14
2011	15
2012	10
2013	7
2014	11
2015	3
2016	4
2017	3
2018	4
2019	2
2020	5
2021	6
2022	4
2023	3
2024	0

1

Pediatric onset Crohn's colitis is characterized by genotype-dependent age-related susceptibility.

Levine A, Kugathasan S, Annese V, Biank V, Leshinsky-Silver E, Davidovich O, Kimmel G, Shamir R, Palmieri O, Karban A, Broeckel U, Cucchiara S. Levine A, et al. Inflamm Bowel Dis. 2007 Dec;13(12):1509-15. doi: 10.1002/ibd.20244. Inflamm Bowel Dis. 2007. PMID: 17763471

2

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. Gazouli M, et al. Eur J Gastroenterol Hepatol. 2004 Nov;16(11):1177-82. doi: 10.1097/00042737-200411000-00016. Eur J Gastroenterol Hepatol. 2004. PMID: 15489579

3

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. Bianchi V, et al. Eur J Gastroenterol Hepatol. 2007 Mar;19(3):217-23. doi: 10.1097/01.meg.0000250590.84102.12. Eur J Gastroenterol Hepatol. 2007. PMID: 17301648

4

A polymorphism in the TNF-alpha promoter gene is associated with pediatric onset and colonic location of Crohn's disease.

Levine A, Karban A, Eliakim R, Shaoul R, Reif S, Pacht A, Wardi J, Yakir B, Silver EL. Levine A, et al. Am J Gastroenterol. 2005 Feb;100(2):407-13. doi: 10.1111/j.1572-0241.2005.41126.x. Am J Gastroenterol. 2005. PMID: 15667501

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. Gazouli M, et al. World J Gastroenterol. 2010 Apr 14;16(14):1753-8. doi: 10.3748/wjg.v16.i14.1753. World J Gastroenterol. 2010. PMID: 20380008 Free PMC article.

6

[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. Lakatos L, et al. Orv Hetil. 2004 Jul 4;145(27):1403-11. Orv Hetil. 2004. PMID: 15320482 Hungarian.

7

Genetic susceptibility has a more important role in pediatric-onset Crohn's disease than in adult-onset Crohn's disease.

de Ridder L, Weersma RK, Dijkstra G, van der Steege G, Benninga MA, Nolte IM, Taminiau JA, Hommes DW, Stokkers PC. de Ridder L, et al. Inflamm Bowel Dis. 2007 Sep;13(9):1083-92. doi: 10.1002/ibd.20171. Inflamm Bowel Dis. 2007. PMID: 17476680

8

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. Heresbach D, et al. Eur J Gastroenterol Hepatol. 2004 Jan;16(1):55-62. doi: 10.1097/00042737-200401000-00009. Eur J Gastroenterol Hepatol. 2004. PMID: 15095853

9

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. Büning C, et al. Aliment Pharmacol Ther. 2004 May 15;19(10):1073-8. doi: 10.1111/j.1365-2036.2004.01967.x. Aliment Pharmacol Ther. 2004. PMID: 15142196 Free article.

10

NOD2/CARD15 variants are associated with lower weight at diagnosis in children with Crohn's disease.

Tomer G, Ceballos C, Concepcion E, Benkov KJ. Tomer G, et al. Am J Gastroenterol. 2003 Nov;98(11):2479-84. doi: 10.1111/j.1572-0241.2003.08673.x. Am J Gastroenterol. 2003. PMID: 14638352

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