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205 results on '"Janine Büttner"'

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1. Long-term results of teduglutide treatment for chronic intestinal failure – Insights from a national, multi-centric patient home-care service program

2. Impact of Laparoscopic Sleeve Gastrectomy on Gut Permeability in Morbidly Obese Subjects

3. Short-Term Overfeeding with Dairy Cream Does Not Modify Gut Permeability, the Fecal Microbiota, or Glucose Metabolism in Young Healthy Men

7. A Promoter Variant Within the Aryl Hydrocarbon Receptor Gene Is Associated with an Epithelial Barrier Defect in Smokers with Crohnʼs Disease

8. Effect of caloric restriction on gut permeability, inflammation markers, and fecal microbiota in obese women

9. PTGER4 modulating variants in Crohn’s disease

10. P2B.14: Predictive Potential of Biomarkers of Intestinal Barrier Function for Therapeutic Management with Teduglutide in Patients with Short Bowel Syndrome

11. 250.6: Results of a Multicentric Retrolective Study of Teduglutide Treatment in Benign Short Bowel Syndrome in Germany

12. Increased small intestinal permeability in ulcerative colitis: Rather genetic than environmental and a risk factor for extensive disease?

13. The JAK2 variant rs10758669 in Crohn’s disease: altering the intestinal barrier as one mechanism of action

14. Hereditary Apolipoprotein AI-Associated Amyloidosis in Surgical Pathology Specimens

15. Prevalence of Germline Mutations in the TTR Gene in a Consecutive Series of Surgical Pathology Specimens With ATTR Amyloid

16. Mutational analysis of ATP7B gene in Egyptian children with Wilson disease: 12 novel mutations

17. A study in three European IBD cohorts confirms that the ATG16L1 c.898A>G (p.Thr300Ala) variant is a susceptibility factor for Crohn’s disease

18. Heterozygosity for IL23R p.Arg381Gln confers a protective effect not only against Crohn’s disease but also ulcerative colitis

19. Importance of rare and private NOD2 variants in foreseeing severe disease behavior in Crohn's disease

20. Clinical features of hemolysis, elevated liver enzymes, and low platelet count syndrome in undiagnosed Wilson disease: report of two cases

21. Laron Syndrome

22. Lymphocytic Hypophysitis

23. Lutembacher’s Syndrome

24. Laryngotracheobronchitis

25. Liver Cirrhosis, Cryptogenic

26. Leukocytoclastic Vasculitis

27. Linear IgA Dermatosis

28. Leg Jerks

29. Large Granular Lymphocyte Leukemia

30. Limb Girdle Muscular Dystrophy Autosomal Recessive Type 2I

31. Low-molecular-Weight Proteinuria with Hypercalciuria and Nephrocalcinosis

32. Lesch-Nyhan Disease

33. LEOPARD Syndrome

34. Lenegre-Lev Syndrome

35. Lesch-Nyhan Variant

36. Limbic Epilepsy

37. Leukemia, Chronic Lymphocytic

38. Limbic Encephalitis

39. Lattice Corneal Dystrophy Type I

40. Legg-Calvé-Perthes' Disease

41. Lewy Body Dementia

42. Lactose Intolerance

43. Legasthenia

44. Linear IgA Bullous Dermatosis

45. Lesion-associated Partial Epilepsies

46. Leukocyte Adhesion Deficiency Syndromes

47. LBBB

48. LVWM

49. LCP

50. Léri-Weill Dyschondrosteosis

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