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2. Assessing adherence to objective disease monitoring and outcomes with adalimumab in a real-world IBD cohort

4. P727 Change in Crohn's disease behavior in a prospective European population-based inception cohort – the ECCO-EpiCom cohort

5. P734 The sex ratio of inflammatory bowel disease varies according to age at onset: results from a worldwide survey

7. P623 Therapeutic preferences and outcomes in newly diagnosed patient with inflammatory bowel diseases in the biological era in Hungary. A nationwide study based on the National Health Insurance Fund database

8. P331 Final results on efficacy and safety of biosimilar infliximab after one-year: results from a prospective nationwide cohort

9. P592 Final results on immunogenicity profile and predictors of ADA development of biosimilar infliximab during the first 12 months of the therapy: results from a prospective nationwide cohort

11. P675 Infliximab biosimilar CT-P13 therapy is effective in maintaining clinical remission in Crohn's disease and ulcerative colitis – 54 week data

15. Infliximab Reduces Endoscopic, but Not Clinical, Recurrence of Crohn’s Disease After Ileocolonic Resection

16. Incidence and initial disease course of inflammatory bowel diseases in 2011 in Europe and Australia: Results of the 2011 ECCO-EpiCom inception cohort

17. Health care and patients' education in a European inflammatory bowel disease inception cohort: An ECCO-EpiCom study

18. Environmental factors in a population-based inception cohort of inflammatory bowel disease patients in Europe — An ECCO-EpiCom study

19. P557 Antibody and cell-mediated immune response to whole virion and split virion influenza vaccine in patients with inflammatory bowel disease on maintenance immunosuppressive and biological therapy

20. P321 The one-year efficacy of infliximab does not depend on the timing of biological therapy in ulcerative colitis

22. DOP028 Development of red flags for early referral of adults with symptoms and signs suggestive of Crohn's disease: an IOIBD initiative

24. P344 Short and medium term efficacy of adalimumab in ulcerative colitis – a multicentre, prospective observational study

28. 183 MANNOSE-BINDING LECTIN DEFICIENCY CONFERS RISK FOR INFECTIONS IN A LARGE HUNGARIAN COHORT OF PATIENTS WITH LIVER CIRRHOSIS

31. P129 - The impact of concomitant treatment with immuno-modulators and antibiotics on the outcome of C. difficile-associated inflammatory bowel disease exacerbation: an ECCO multi-center retrospective study

33. P295 - MBL level and deficiency is not associated with either Crohn's disease or ulcerative colitis, disease phenotype, CRP, serology profile and NOD2/CARD15 genotype in a large Hungarian IBD cohort, but was associated to the lack of TLR4 variants in CD

34. P015 - Pancreatic autoantibodies are associated with reactivity to microbial antibodies penetrating disease behavior perianal disease and extraintestinal manifestations but not with NOD2/CARD15 or TLR4 genotype in a Hungarian IBD cohort

35. ATG16L1 and IL23 receptor (IL23R) genes are associated with disease susceptibility in Hungarian CD patients

36. European evidence-based Consensus on the diagnosis and management of ulcerative colitis: Definitions and diagnosis

37. P285 COMPARING CONVENTIONAL AND GASCA TESTS FOR THE DIAGNOSIS AND DETERMINATION OF CLINICAL PHENOTYPE IN CROHN'S DISEASE

38. P209 NFKBIA 3'UTR AND NFKB1 -94INS/DELATTG VARIANTS IN HUNGARIAN IBD PATIENTS: THE 3'UTR VARIANT IS ASSOCIATED WITH EXTENSIVE COLITIS

42. P253 NEW SEROLOGICAL MARKERS FOR INFLAMMATORY BOWEL DISEASE ARE ASSOCIATED WITH EARLIER AGE AT ONSET, COMPLICATED DISEASE BEHAVIOR, RISK FOR SURGERY, AND NOD2/CARD15 GENOTYPE IN A HUNGARIAN IBD COHORT

44. NOD1 gene E266K polymorphism is associated with disease susceptibility but not with disease phenotype or NOD2/CARD15 in Hungarian patients with Crohn's disease

45. P120 THE ATP-BINDING CASSETTE TRANSPORTER ABCG2 (BCRP) AND ABCB1 (MDR1) VARIANTS ARE NOT ASSOCIATED WITH DISEASE SUSCEPTIBILITY, DISEASE PHENOTYPE, RESPONSE TO MEDICAL THERAPY OR NEED FOR SURGERY IN HUNGARIAN PATIENTS WITH INFLAMMATORY BOWEL DISEASES

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