These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

134 related items for PubMed ID: 12563685

  • 1. NOD2/CARD15 gene mutation is not associated with susceptibility to Wegener's granulomatosis.
    Newman B, Rubin LA, Siminovitch KA.
    J Rheumatol; 2003 Feb; 30(2):305-7. PubMed ID: 12563685
    [Abstract] [Full Text] [Related]

  • 2. [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 04; 145(27):1403-11. PubMed ID: 15320482
    [Abstract] [Full Text] [Related]

  • 3. 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 04; 98(11):2479-84. PubMed ID: 14638352
    [Abstract] [Full Text] [Related]

  • 4. 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 04; 97(12):3095-101. PubMed ID: 12492195
    [Abstract] [Full Text] [Related]

  • 5. 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 04; 42(11):1380-2. PubMed ID: 12810925
    [Abstract] [Full Text] [Related]

  • 6. CARD15 mutations in patients with Crohn's disease in a homogeneous Spanish population.
    Núñez C, Barreiro M, Domínguez-Muñoz JE, Lorenzo A, Zapata C, Peña AS.
    Am J Gastroenterol; 2004 Mar 04; 99(3):450-6. PubMed ID: 15056084
    [Abstract] [Full Text] [Related]

  • 7. Absence of mutation in the NOD2/CARD15 gene among 483 Japanese patients with Crohn's disease.
    Yamazaki K, Takazoe M, Tanaka T, Kazumori T, Nakamura Y.
    J Hum Genet; 2002 Mar 04; 47(9):469-72. PubMed ID: 12202985
    [Abstract] [Full Text] [Related]

  • 8. 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 04; 99(6):1134-40. PubMed ID: 15180737
    [Abstract] [Full Text] [Related]

  • 9. CARD15 gene polymorphisms in patients with spondyloarthropathies identify a specific phenotype previously related to Crohn's disease.
    Laukens D, Peeters H, Marichal D, Vander Cruyssen B, Mielants H, Elewaut D, Demetter P, Cuvelier C, Van Den Berghe M, Rottiers P, Veys EM, Remaut E, Steidler L, De Keyser F, De Vos M.
    Ann Rheum Dis; 2005 Jun 04; 64(6):930-5. PubMed ID: 15539413
    [Abstract] [Full Text] [Related]

  • 10. Crohn's disease-associated NOD2 variants share a signaling defect in response to lipopolysaccharide and peptidoglycan.
    Bonen DK, Ogura Y, Nicolae DL, Inohara N, Saab L, Tanabe T, Chen FF, Foster SJ, Duerr RH, Brant SR, Cho JH, Nuñez G.
    Gastroenterology; 2003 Jan 04; 124(1):140-6. PubMed ID: 12512038
    [Abstract] [Full Text] [Related]

  • 11. 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 04; 145(2):208-12. PubMed ID: 15289769
    [Abstract] [Full Text] [Related]

  • 12. Clinical applications of NOD2/CARD15 mutations in Crohn's disease.
    Barreiro-de Acosta M, Peña AS.
    Acta Gastroenterol Latinoam; 2007 Mar 04; 37(1):49-54. PubMed ID: 17486745
    [Abstract] [Full Text] [Related]

  • 13. Host susceptibility to tuberculosis: CARD15 polymorphisms in a South African population.
    Möller M, Nebel A, Kwiatkowski R, van Helden PD, Hoal EG, Schreiber S.
    Mol Cell Probes; 2007 Apr 04; 21(2):148-51. PubMed ID: 17113749
    [Abstract] [Full Text] [Related]

  • 14. Analysis of CARD15 polymorphisms in Korean patients with ankylosing spondylitis reveals absence of common variants seen in western populations.
    Kim TH, Rahman P, Jun JB, Lee HS, Park YW, Im HJ, Snelgrove T, Peddle L, Hallett D, Inman RD.
    J Rheumatol; 2004 Oct 04; 31(10):1959-61. PubMed ID: 15468360
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. CARD15/NOD2 single nucleotide polymorphisms do not confer susceptibility to type I psoriasis.
    Plant D, Lear J, Marsland A, Worthington J, Griffiths CE.
    Br J Dermatol; 2004 Sep 15; 151(3):675-8. PubMed ID: 15377357
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. CARD15 mutations in familial granulomatosis syndromes: a study of the original Blau syndrome kindred and other families with large-vessel arteritis and cranial neuropathy.
    Wang X, Kuivaniemi H, Bonavita G, Mutkus L, Mau U, Blau E, Inohara N, Nunez G, Tromp G, Williams CJ.
    Arthritis Rheum; 2002 Nov 15; 46(11):3041-5. PubMed ID: 12428248
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.