134 related articles for article (PubMed ID: 26438151)
1. The common NOD2/CARD15 variant P268S in patients with non-infectious uveitis: a cohort study.
Marrani E; Cimaz R; Lucherini OM; Caputo R; Vitale A; Cantarini L; Simonini G
Pediatr Rheumatol Online J; 2015 Oct; 13(1):38. PubMed ID: 26438151
[TBL] [Abstract][Full Text] [Related]
2. Blau syndrome-related CARD15/NOD2 mutations are not linked to idiopathic uveitis in Spanish patients.
Rodríguez-Pérez N; Aguinaga-Barrilero A; Gorroño-Echebarría MB; Pérez-Blas M; Martín-Villa JM
Dis Markers; 2009; 27(1):1-5. PubMed ID: 19822951
[TBL] [Abstract][Full Text] [Related]
3. Blau syndrome associated with a CARD15/NOD2 mutation.
Snyers B; Dahan K
Am J Ophthalmol; 2006 Dec; 142(6):1089-92. PubMed ID: 17157607
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Importance of NOD2/CARD15 gene variants for susceptibility to and outcome of sepsis in Turkish children.
Tekin D; Dalgic N; Kayaalti Z; Soylemezoglu T; Diler B; Kutlubay BI
Pediatr Crit Care Med; 2012 Mar; 13(2):e73-7. PubMed ID: 21460759
[TBL] [Abstract][Full Text] [Related]
6. A Novel NOD2-associated Mutation and Variant Blau Syndrome: Phenotype and Molecular Analysis.
Ebrahimiadib N; Samra KA; Domina AM; Stiles ER; Ewer R; Bocian CP; Foster CS
Ocul Immunol Inflamm; 2018; 26(1):57-64. PubMed ID: 27419275
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. NOD2/CARD15 gene mutation identified in a Chinese family with Blau syndrome.
Xiang H; Zhang T; Chen M; Zhou X; Li Z; Yan N; Li S; Han Y; Gong Q; Liu X
Mol Vis; 2012; 18():617-23. PubMed ID: 22509093
[TBL] [Abstract][Full Text] [Related]
9. Familial case of Blau syndrome associated with a CARD15/NOD2 mutation.
Villanueva-Mendoza C; Arellanes-García L; Cubas-Lorenzo V; Jimenez-Martinez MC; Flores-Suárez LF; Zenteno JC
Ophthalmic Genet; 2010 Sep; 31(3):155-8. PubMed ID: 20565245
[TBL] [Abstract][Full Text] [Related]
10. Role of the NOD2 genotype in the clinical phenotype of Blau syndrome and early-onset sarcoidosis.
Okafuji I; Nishikomori R; Kanazawa N; Kambe N; Fujisawa A; Yamazaki S; Saito M; Yoshioka T; Kawai T; Sakai H; Tanizaki H; Heike T; Miyachi Y; Nakahata T
Arthritis Rheum; 2009 Jan; 60(1):242-50. PubMed ID: 19116920
[TBL] [Abstract][Full Text] [Related]
11. Ocular manifestations in Blau syndrome associated with a CARD15/Nod2 mutation.
Kurokawa T; Kikuchi T; Ohta K; Imai H; Yoshimura N
Ophthalmology; 2003 Oct; 110(10):2040-4. PubMed ID: 14522785
[TBL] [Abstract][Full Text] [Related]
12. NOD2/CARD15 gene mutations in patients with gouty arthritis.
Karaarslan A; Kobak S; Berdeli A
Bosn J Basic Med Sci; 2016 Nov; 16(4):276-279. PubMed ID: 27357501
[TBL] [Abstract][Full Text] [Related]
13. The role of NOD1/CARD4 and NOD2/CARD15 genetic variations in lung cancer risk.
Ozbayer C; Kurt H; Bayramoglu A; Gunes HV; Metintas M; Degirmenci İ; Oner KS
Inflamm Res; 2015 Oct; 64(10):775-9. PubMed ID: 26238283
[TBL] [Abstract][Full Text] [Related]
14. Uveitis in patients with sarcoidosis is not associated with mutations in NOD2 (CARD15).
Martin TM; Doyle TM; Smith JR; Dinulescu D; Rust K; Rosenbaum JT
Am J Ophthalmol; 2003 Nov; 136(5):933-5. PubMed ID: 14597055
[TBL] [Abstract][Full Text] [Related]
15. A novel mutation in the NOD2 gene associated with Blau syndrome: a Norwegian family with four affected members.
Milman N; Ursin K; Rødevand E; Nielsen FC; Hansen TV
Scand J Rheumatol; 2009; 38(3):190-7. PubMed ID: 19169908
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. NOD2 gene-associated pediatric granulomatous arthritis: clinical diversity, novel and recurrent mutations, and evidence of clinical improvement with interleukin-1 blockade in a Spanish cohort.
Aróstegui JI; Arnal C; Merino R; Modesto C; Antonia Carballo M; Moreno P; García-Consuegra J; Naranjo A; Ramos E; de Paz P; Rius J; Plaza S; Yagüe J
Arthritis Rheum; 2007 Nov; 56(11):3805-13. PubMed ID: 17968944
[TBL] [Abstract][Full Text] [Related]
18. [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]
19. 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]
20. Evidence of allelic heterogeneity for associations between the NOD2/CARD15 gene and ulcerative colitis among North Indians.
Juyal G; Amre D; Midha V; Sood A; Seidman E; Thelma BK
Aliment Pharmacol Ther; 2007 Nov; 26(10):1325-32. PubMed ID: 17892524
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]