258 related articles for article (PubMed ID: 23562557)
21.
Berlin P; Reiner J; Witte M; Wobar J; Lindemann S; Barrantes I; Kreikemeyer B; Bastian M; Schäffler H; Bannert K; Jaster R; Lamprecht G
Am J Physiol Gastrointest Liver Physiol; 2019 Nov; 317(5):G727-G738. PubMed ID: 31509436
[TBL] [Abstract][Full Text] [Related]
22. CARD15/NOD2 polymorphisms do not explain concordance of Crohn's disease in Swedish monozygotic twins.
Halfvarson J; Bresso F; D'Amato M; Järnerot G; Pettersson S; Tysk C
Dig Liver Dis; 2005 Oct; 37(10):768-72. PubMed ID: 16002353
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. 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]
25. Molecular prediction of disease risk and severity in a large Dutch Crohn's disease cohort.
Weersma RK; Stokkers PC; van Bodegraven AA; van Hogezand RA; Verspaget HW; de Jong DJ; van der Woude CJ; Oldenburg B; Linskens RK; Festen EA; van der Steege G; Hommes DW; Crusius JB; Wijmenga C; Nolte IM; Dijkstra G;
Gut; 2009 Mar; 58(3):388-95. PubMed ID: 18824555
[TBL] [Abstract][Full Text] [Related]
26. Increased intestinal permeability and NOD2 variants in familial and sporadic Crohn's disease.
D'Incà R; Annese V; di Leo V; Latiano A; Quaino V; Abazia C; Vettorato MG; Sturniolo GC
Aliment Pharmacol Ther; 2006 May; 23(10):1455-61. PubMed ID: 16669960
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. The NOD2 single nucleotide polymorphisms rs2066843 and rs2076756 are novel and common Crohn's disease susceptibility gene variants.
Glas J; Seiderer J; Tillack C; Pfennig S; Beigel F; Jürgens M; Olszak T; Laubender RP; Weidinger M; Müller-Myhsok B; Göke B; Ochsenkühn T; Lohse P; Diegelmann J; Czamara D; Brand S
PLoS One; 2010 Dec; 5(12):e14466. PubMed ID: 21209938
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. 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]
31. Perianal disease combined with NOD2 genotype predicts need for IBD-related surgery in Crohn's disease patients from a population-based cohort.
Nasir BF; Griffiths L; Nasir A; Roberts R; Barclay M; Gearry R; Lea RA
J Clin Gastroenterol; 2013 Mar; 47(3):242-5. PubMed ID: 22739221
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Crohn's disease patients with chronic intestinal failure receiving long-term parenteral nutrition: a cross-national adult study.
Elriz K; Palascak-Juif V; Joly F; Seguy D; Beau P; Chambrier C; Boncompain M; Fontaine E; Laharie D; Savoye G; Lerebours E
Aliment Pharmacol Ther; 2011 Oct; 34(8):931-40. PubMed ID: 21848855
[TBL] [Abstract][Full Text] [Related]
34. A distinct pattern of disease-associated single nucleotide polymorphisms in IBD risk genes in a family with Crohn's disease.
Barthel C; Spalinger MR; Brunner J; Lang S; Fried M; Rogler G; Scharl M
Eur J Gastroenterol Hepatol; 2014 Jul; 26(7):803-6. PubMed ID: 24901824
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. 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]
37. 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]
38. 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]
39. Associations of NOD2 polymorphisms with Erysipelotrichaceae in stool of in healthy first degree relatives of Crohn's disease subjects.
Turpin W; Bedrani L; Espin-Garcia O; Xu W; Silverberg MS; Smith MI; Garay JAR; Lee SH; Guttman DS; Griffiths A; Moayyedi P; Panaccione R; Huynh H; Steinhart HA; Aumais G; Dieleman LA; Turner D; ; Paterson AD; Croitoru K
BMC Med Genet; 2020 Oct; 21(1):204. PubMed ID: 33059653
[TBL] [Abstract][Full Text] [Related]
40. Development of a uniform, very aggressive disease phenotype in all homozygous carriers of the NOD2 mutation p.Leu1007fsX1008 with Crohn's disease and active smoking status resulting in ileal stenosis requiring surgery.
Schnitzler F; Friedrich M; Angelberger M; Diegelmann J; Stallhofer J; Wolf C; Dütschler J; Truniger S; Olszak T; Beigel F; Tillack C; Lohse P; Brand S
PLoS One; 2020; 15(7):e0236421. PubMed ID: 32716958
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]