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Journal Abstract Search
161 related items for PubMed ID: 12810925
1. CARD15/NOD2 analysis in rheumatoid arthritis susceptibility. Ferreirós-Vidal I, Barros F, Pablos JL, Carracedo A, Gómez-Reino JJ, Gonzalez A. Rheumatology (Oxford); 2003 Nov; 42(11):1380-2. PubMed ID: 12810925 [Abstract] [Full Text] [Related]
4. 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. PubMed ID: 15180737 [Abstract] [Full Text] [Related]
5. Variation at NOD2/CARD15 in familial and sporadic cases of Crohn's disease in the Ashkenazi Jewish population. Zhou Z, Lin XY, Akolkar PN, Gulwani-Akolkar B, Levine J, Katz S, Silver J. Am J Gastroenterol; 2002 Dec; 97(12):3095-101. PubMed ID: 12492195 [Abstract] [Full Text] [Related]
6. 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. PubMed ID: 15142196 [Abstract] [Full Text] [Related]
9. NOD2/CARD15 gene mutation is not associated with susceptibility to Wegener's granulomatosis. Newman B, Rubin LA, Siminovitch KA. J Rheumatol; 2003 Feb 15; 30(2):305-7. PubMed ID: 12563685 [Abstract] [Full Text] [Related]
10. 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 15; 37(10):768-72. PubMed ID: 16002353 [Abstract] [Full Text] [Related]
11. Exclusion of CARD15/NOD2 as a candidate susceptibility gene to psoriasis in the Italian population. Borgiani P, Vallo L, D'Apice MR, Giardina E, Pucci S, Capon F, Nisticò S, Chimenti S, Pallone F, Novelli G. Eur J Dermatol; 2002 Oct 15; 12(6):540-2. PubMed ID: 12459523 [Abstract] [Full Text] [Related]
13. Genetic basis for increased intestinal permeability in families with Crohn's disease: role of CARD15 3020insC mutation? Buhner S, Buning C, Genschel J, Kling K, Herrmann D, Dignass A, Kuechler I, Krueger S, Schmidt HH, Lochs H. Gut; 2006 Mar 15; 55(3):342-7. PubMed ID: 16000642 [Abstract] [Full Text] [Related]