214 related articles for article (PubMed ID: 16819374)
1. Ileal lymphonodular hyperplasia is not associated with NOD2/CARD15 mutations.
Shaoul R; Eliakim R; Tamir A; Karban A
J Pediatr Gastroenterol Nutr; 2006 Jul; 43(1):30-4. PubMed ID: 16819374
[TBL] [Abstract][Full Text] [Related]
2. 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
[TBL] [Abstract][Full Text] [Related]
3. 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; 145(2):208-12. PubMed ID: 15289769
[TBL] [Abstract][Full Text] [Related]
4. 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. PubMed ID: 17301648
[TBL] [Abstract][Full Text] [Related]
5. Clinical applications of NOD2/CARD15 mutations in Crohn's disease.
Barreiro-de Acosta M; Peña AS
Acta Gastroenterol Latinoam; 2007 Mar; 37(1):49-54. PubMed ID: 17486745
[TBL] [Abstract][Full Text] [Related]
6. 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. PubMed ID: 17852840
[TBL] [Abstract][Full Text] [Related]
7. 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. PubMed ID: 17101573
[TBL] [Abstract][Full Text] [Related]
8. Crohn's disease is associated with polymorphism of CARD15/NOD2 gene in a Hungarian population.
Nagy Z; Karádi O; Rumi G; Rumi G; Pár A; Mózsik G; Czirják L; Süto G
Ann N Y Acad Sci; 2005 Jun; 1051():45-51. PubMed ID: 16126943
[TBL] [Abstract][Full Text] [Related]
9. NOD2/CARD15 gene variants are linked to failure of antibiotic treatment in perianal fistulating Crohn's disease.
Angelberger S; Reinisch W; Dejaco C; Miehsler W; Waldhoer T; Wehkamp J; Lichtenberger C; Schaeffeler E; Vogelsang H; Schwab M; Teml A
Am J Gastroenterol; 2008 May; 103(5):1197-202. PubMed ID: 18371140
[TBL] [Abstract][Full Text] [Related]
10. CARD15 mutations in Dutch familial and sporadic inflammatory bowel disease and an overview of European studies.
van der Linde K; Boor PP; Houwing-Duistermaat JJ; Crusius BJ; Wilson PJ; Kuipers EJ; de Rooij FW
Eur J Gastroenterol Hepatol; 2007 Jun; 19(6):449-59. PubMed ID: 17489054
[TBL] [Abstract][Full Text] [Related]
11. 3020insC insertion in NOD2/CARD15 gene, a prevalent variant associated with anti-Saccharomyces cerevisiae antibodies and ileal location of Crohn's disease in Tunisian population.
Marrakchi R; Bougatef K; Moussa A; Ouerhani S; Khodjet-el-Khil H; Messai Y; Mestiri O; Najar T; Benammar-Elgaaeid A
Inflamm Res; 2009 Apr; 58(4):218-23. PubMed ID: 19184350
[TBL] [Abstract][Full Text] [Related]
12. [Does smoking influence the course of Crohn's disease in patients with the presence of gene NOD2/CARD15 mutation?].
Dobrowolska-Zachwieja A; Kaczmarek M; Hoppe-Gołebiewska J; Kalak R; Słomski R; Linke K
Pol Merkur Lekarski; 2005 May; 18(107):560-5. PubMed ID: 16161956
[TBL] [Abstract][Full Text] [Related]
13. New serological markers for inflammatory bowel disease are associated with earlier age at onset, complicated disease behavior, risk for surgery, and NOD2/CARD15 genotype in a Hungarian IBD cohort.
Papp M; Altorjay I; Dotan N; Palatka K; Foldi I; Tumpek J; Sipka S; Udvardy M; Dinya T; Lakatos L; Kovacs A; Molnar T; Tulassay Z; Miheller P; Norman GL; Szamosi T; Papp J; ; Lakatos PL
Am J Gastroenterol; 2008 Mar; 103(3):665-81. PubMed ID: 18047543
[TBL] [Abstract][Full Text] [Related]
14. 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. PubMed ID: 18090989
[TBL] [Abstract][Full Text] [Related]
15. Is age of onset of Crohn's disease governed by mutations in NOD2/caspase recruitment domains 15 and Toll-like receptor 4? Evaluation of a pediatric cohort.
Leshinsky-Silver E; Karban A; Buzhakor E; Fridlander M; Yakir B; Eliakim R; Reif S; Shaul R; Boaz M; Lev D; Levine A
Pediatr Res; 2005 Sep; 58(3):499-504. PubMed ID: 16148063
[TBL] [Abstract][Full Text] [Related]
16. The V249I polymorphism of the CX3CR1 gene is associated with fibrostenotic disease behavior in patients with Crohn's disease.
Sabate JM; Ameziane N; Lamoril J; Jouet P; Farmachidi JP; Soulé JC; Harnois F; Sobhani I; Jian R; Deybach JC; de Prost D; Coffin B
Eur J Gastroenterol Hepatol; 2008 Aug; 20(8):748-55. PubMed ID: 18617779
[TBL] [Abstract][Full Text] [Related]
17. NOD2 sequencing in Iranian children with Crohn's disease.
Motamed F; Najafi M; Taghvaei M; Moazzami K; Farahmand F; Khodadad A; Fallahi GH; Parvaneh N; Khatami GR; Rezaei N
Z Gastroenterol; 2011 Jul; 49(12):1526-8. PubMed ID: 22139875
[TBL] [Abstract][Full Text] [Related]
18. NOD2 mutations predict the risk for surgery in pediatric-onset Crohn's disease.
Lacher M; Helmbrecht J; Schroepf S; Koletzko S; Ballauff A; Classen M; Uhlig H; Hubertus J; Hartl D; Lohse P; von Schweinitz D; Kappler R
J Pediatr Surg; 2010 Aug; 45(8):1591-7. PubMed ID: 20713205
[TBL] [Abstract][Full Text] [Related]
19. Identification of NOD2/CARD15 mutations in Malaysian patients with Crohn's disease.
Chua KH; Hilmi I; Ng CC; Eng TL; Palaniappan S; Lee WS; Goh KL
J Dig Dis; 2009 May; 10(2):124-30. PubMed ID: 19426395
[TBL] [Abstract][Full Text] [Related]
20. CARD15 variants in patients with sporadic Parkinson's disease.
Bialecka M; Kurzawski M; Klodowska-Duda G; Opala G; Juzwiak S; Kurzawski G; Tan EK; Drozdzik M
Neurosci Res; 2007 Mar; 57(3):473-6. PubMed ID: 17174426
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]