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Journal Abstract Search

435 related items for PubMed ID: 16244543

  • 1. Crohn's disease patients carrying Nod2/CARD15 gene variants have an increased and early need for first surgery due to stricturing disease and higher rate of surgical recurrence.
    Alvarez-Lobos M, Arostegui JI, Sans M, Tassies D, Plaza S, Delgado S, Lacy AM, Pique JM, Yagüe J, Panés J.
    Ann Surg; 2005 Nov; 242(5):693-700. PubMed ID: 16244543
    [Abstract] [Full Text] [Related]

  • 2. NOD2/CARD15 gene polymorphisms in Crohn's disease: a genotype- phenotype analysis.
    Heresbach D, Gicquel-Douabin V, Birebent B, D'halluin PN, Heresbach-Le Berre N, Dreano S, Siproudhis L, Dabadie A, Gosselin M, Mosser J, Semana G, Bretagne JF, Yaouanq J.
    Eur J Gastroenterol Hepatol; 2004 Jan; 16(1):55-62. PubMed ID: 15095853
    [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; 98(11):2479-84. PubMed ID: 14638352
    [Abstract] [Full Text] [Related]

  • 4. Genotype-phenotype analysis in childhood-onset Crohn's disease: NOD2/CARD15 variants consistently predict phenotypic characteristics of severe disease.
    Russell RK, Drummond HE, Nimmo EE, Anderson N, Smith L, Wilson DC, Gillett PM, McGrogan P, Hassan K, Weaver LT, Bisset M, Mahdi G, Satsangi J.
    Inflamm Bowel Dis; 2005 Nov; 11(11):955-64. PubMed ID: 16239840
    [Abstract] [Full Text] [Related]

  • 5. Combined type-1 plasminogen activator inhibitor and NOD2/CARD15 genotyping predicts complicated Crohn's disease behaviour.
    Alvarez-Lobos M, Arostegui JI, Sans M, Tassies D, Piu J, Reverter JC, Pique JM, Yagüe J, Panés J.
    Aliment Pharmacol Ther; 2007 Feb 15; 25(4):429-40. PubMed ID: 17269998
    [Abstract] [Full Text] [Related]

  • 6. CARD15 gene variants and risk of reoperation in Crohn's disease patients.
    Maconi G, Colombo E, Sampietro GM, Lamboglia F, D'Incà R, Daperno M, Cassinotti A, Sturniolo GC, Ardizzone S, Duca P, Porro GB, Annese V.
    Am J Gastroenterol; 2009 Oct 15; 104(10):2483-91. PubMed ID: 19638967
    [Abstract] [Full Text] [Related]

  • 7. Prediction of Crohn's disease aggression through NOD2/CARD15 gene sequencing in an Australian cohort.
    Bhullar M, Macrae F, Brown G, Smith M, Sharpe K.
    World J Gastroenterol; 2014 May 07; 20(17):5008-16. PubMed ID: 24803813
    [Abstract] [Full Text] [Related]

  • 8. Gastroduodenal Crohn's disease is associated with NOD2/CARD15 gene polymorphisms, particularly L1007P homozygosity.
    Mardini HE, Gregory KJ, Nasser M, Selby L, Arsenescu R, Winter TA, de Villiers WJ.
    Dig Dis Sci; 2005 Dec 07; 50(12):2316-22. PubMed ID: 16416181
    [Abstract] [Full Text] [Related]

  • 9. 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 07; 97(12):3095-101. PubMed ID: 12492195
    [Abstract] [Full Text] [Related]

  • 10. 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 07; 99(6):1134-40. PubMed ID: 15180737
    [Abstract] [Full Text] [Related]

  • 11. Early development of stricturing or penetrating pattern in Crohn's disease is influenced by disease location, number of flares, and smoking but not by NOD2/CARD15 genotype.
    Louis E, Michel V, Hugot JP, Reenaers C, Fontaine F, Delforge M, El Yafi F, Colombel JF, Belaiche J.
    Gut; 2003 Apr 07; 52(4):552-7. PubMed ID: 12631668
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  • 13. Carriage of CARD15 variants and smoking as risk factors for resective surgery in patients with Crohn's ileal disease.
    Laghi L, Costa S, Saibeni S, Bianchi P, Omodei P, Carrara A, Spina L, Contessini Avesani E, Vecchi M, De Franchis R, Malesci A.
    Aliment Pharmacol Ther; 2005 Sep 15; 22(6):557-64. PubMed ID: 16167972
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  • 16. CARD15 gene mutations and risk for early surgery in pediatric-onset Crohn's disease.
    Kugathasan S, Collins N, Maresso K, Hoffmann RG, Stephens M, Werlin SL, Rudolph C, Broeckel U.
    Clin Gastroenterol Hepatol; 2004 Nov 15; 2(11):1003-9. PubMed ID: 15551253
    [Abstract] [Full Text] [Related]

  • 17. The role of Toll-like receptor 4 Asp299Gly and Thr399Ile polymorphisms and CARD15/NOD2 mutations in the susceptibility and phenotype of Crohn's disease.
    Brand S, Staudinger T, Schnitzler F, Pfennig S, Hofbauer K, Dambacher J, Seiderer J, Tillack C, Konrad A, Crispin A, Göke B, Lohse P, Ochsenkühn T.
    Inflamm Bowel Dis; 2005 Jul 15; 11(7):645-52. PubMed ID: 15973118
    [Abstract] [Full Text] [Related]

  • 18. NOD2/CARD15 mutations in Croatian patients with Crohn's disease: prevalence and genotype-phenotype relationship.
    Cukovic-Cavka S, Vermeire S, Hrstic I, Claessens G, Kolacek S, Jakic-Razumovic J, Krznaric Z, Grubelic K, Radic D, Misak Z, Jadresin O, Rutgeerts P, Vucelic B.
    Eur J Gastroenterol Hepatol; 2006 Aug 15; 18(8):895-9. PubMed ID: 16825909
    [Abstract] [Full Text] [Related]

  • 19. Predictive value of the CARD15 variant 1007fs for the diagnosis of intestinal stenoses and the need for surgery in Crohn's disease in clinical practice: results of a prospective study.
    Seiderer J, Brand S, Herrmann KA, Schnitzler F, Hatz R, Crispin A, Pfennig S, Schoenberg SO, Göke B, Lohse P, Ochsenkuhn T.
    Inflamm Bowel Dis; 2006 Dec 15; 12(12):1114-21. PubMed ID: 17119385
    [Abstract] [Full Text] [Related]

  • 20. 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]

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