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Items: 1 to 20 of 507

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.

Inflamm Bowel Dis. 2007 Dec;13(12):1509-15. Erratum in: Inflamm Bowel Dis. 2008 Dec;14(12):1760. Orazio, Palmieri [corrected to Palmieri, Orazio].

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.

Eur J Gastroenterol Hepatol. 2004 Nov;16(11):1177-82.

PMID:
15489579
3.

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.

Am J Gastroenterol. 2005 Feb;100(2):407-13.

PMID:
15667501
4.

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;20(10):978-84. doi: 10.1097/MEG.0b013e328302f45e.

PMID:
18787464
5.

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;19(3):217-23.

PMID:
17301648
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.

Orv Hetil. 2004 Jul 4;145(27):1403-11. Hungarian.

PMID:
15320482
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.

Inflamm Bowel Dis. 2007 Sep;13(9):1083-92.

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.

Eur J Gastroenterol Hepatol. 2004 Jan;16(1):55-62.

PMID:
15095853
9.

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.

PMID:
15551253
10.

NOD2/CARD15 mutations in Croatian patients with Crohn's disease: prevalence and genotype-phenotype relationship.

Cukovic-Cavka S, Vermeire S, Hrstic I, Claessens G, Kolacek S, Jakic-Razumovic J, Krznaric Z, Grubelic K, Radic D, Misak Z, Jadresin O, Rutgeerts P, Vucelic B.

Eur J Gastroenterol Hepatol. 2006 Aug;18(8):895-9.

PMID:
16825909
11.

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.

12.

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.

PMID:
14638352
13.

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.

PMID:
16239840
14.

Ileal involvement is age dependent in pediatric Crohn's disease.

Meinzer U, Ideström M, Alberti C, Peuchmaur M, Belarbi N, Bellaïche M, Mougenot JF, Cézard JP, Finkel Y, Hugot JP.

Inflamm Bowel Dis. 2005 Jul;11(7):639-44.

PMID:
15973117
15.

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. doi: 10.1111/j.1399-0039.2008.01047.x.

PMID:
18489434
16.

Homozygosity for the CARD15 frameshift mutation 1007fs is predictive of early onset of Crohn's disease with ileal stenosis, entero-enteral fistulas, and frequent need for surgical intervention with high risk of re-stenosis.

Seiderer J, Schnitzler F, Brand S, Staudinger T, Pfennig S, Herrmann K, Hofbauer K, Dambacher J, Tillack C, Sackmann M, Göke B, Lohse P, Ochsenkühn T.

Scand J Gastroenterol. 2006 Dec;41(12):1421-32.

PMID:
17101573
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;42(12):1445-51.

PMID:
17852840
18.

Diverse effects of the CARD15 and IBD5 loci on clinical phenotype in 630 patients with Crohn's disease.

Onnie CM, Fisher SA, Prescott NJ, Mirza MM, Green P, Sanderson J, Forbes A, Lewis CM, Mathew CG.

Eur J Gastroenterol Hepatol. 2008 Jan;20(1):37-45.

PMID:
18090989
19.

CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease.

Lesage S, Zouali H, Cézard JP, Colombel JF, Belaiche J, Almer S, Tysk C, O'Morain C, Gassull M, Binder V, Finkel Y, Modigliani R, Gower-Rousseau C, Macry J, Merlin F, Chamaillard M, Jannot AS, Thomas G, Hugot JP; EPWG-IBD Group; EPIMAD Group; GETAID Group.

Am J Hum Genet. 2002 Apr;70(4):845-57. Epub 2002 Mar 1.

20.

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;99(6):1134-40.

PMID:
15180737

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