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Journal Abstract Search

533 related items for PubMed ID: 12492195

  • 1. 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]

  • 2. 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]

  • 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
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. 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; 124(1):140-6. PubMed ID: 12512038
    [Abstract] [Full Text] [Related]

  • 6. [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]

  • 7. A population-based case-control study of CARD15 and other risk factors in Crohn's disease and ulcerative colitis.
    Brant SR, Wang MH, Rawsthorne P, Sargent M, Datta LW, Nouvet F, Shugart YY, Bernstein CN.
    Am J Gastroenterol; 2007 Feb 04; 102(2):313-23. PubMed ID: 17100976
    [Abstract] [Full Text] [Related]

  • 8. Variants of CARD15 are associated with an aggressive clinical course of Crohn's disease--an IG-IBD study.
    Annese V, Lombardi G, Perri F, D'Incà R, Ardizzone S, Riegler G, Giaccari S, Vecchi M, Castiglione F, Gionchetti P, Cocchiara E, Vigneri S, Latiano A, Palmieri O, Andriulli A.
    Am J Gastroenterol; 2005 Jan 04; 100(1):84-92. PubMed ID: 15654786
    [Abstract] [Full Text] [Related]

  • 9. Analysis of the CARD15 variants R702W, G908R and L1007fs in Italian IBD patients.
    Giachino D, van Duist MM, Regazzoni S, Gregori D, Bardessono M, Salacone P, Scaglione N, Sostegni R, Sapone N, Bresso F, Sambataro A, Gaia E, Pera A, Astegiano M, De Marchi M.
    Eur J Hum Genet; 2004 Mar 04; 12(3):206-12. PubMed ID: 14747834
    [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 04; 19(6):449-59. PubMed ID: 17489054
    [Abstract] [Full Text] [Related]

  • 11. 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 Jun 04; 47(9):469-72. PubMed ID: 12202985
    [Abstract] [Full Text] [Related]

  • 12. 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 15; 23(10):1455-61. PubMed ID: 16669960
    [Abstract] [Full Text] [Related]

  • 13. Clinical applications of NOD2/CARD15 mutations in Crohn's disease.
    Barreiro-de Acosta M, Peña AS.
    Acta Gastroenterol Latinoam; 2007 Mar 15; 37(1):49-54. PubMed ID: 17486745
    [Abstract] [Full Text] [Related]

  • 14. CARD15/NOD2 gene variants are associated with familially occurring and complicated forms of Crohn's disease.
    Heliö T, Halme L, Lappalainen M, Fodstad H, Paavola-Sakki P, Turunen U, Färkkilä M, Krusius T, Kontula K.
    Gut; 2003 Apr 15; 52(4):558-62. PubMed ID: 12631669
    [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
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  • 18. Variants of CARD15, TNFA and PTPN22 and susceptibility to Crohn's disease in the Czech population: high frequency of the CARD15 1007fs.
    Hradsky O, Lenicek M, Dusatkova P, Bronsky J, Nevoral J, Valtrova V, Kotalova R, Szitanyi P, Petro R, Starzykova V, Bortlik M, Vitek L, Lukas M, Cinek O.
    Tissue Antigens; 2008 Jun 15; 71(6):538-47. PubMed ID: 18489434
    [Abstract] [Full Text] [Related]

  • 19. 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 15; 41(12):1421-32. PubMed ID: 17101573
    [Abstract] [Full Text] [Related]

  • 20. 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 15; 10(2):124-30. PubMed ID: 19426395
    [Abstract] [Full Text] [Related]

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