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4. A mild and transient form of autosomal recessive pseudohypoaldosteronism type 1 caused by a novel mutation in the SCNN1A gene.

7. Epithelial Na+ Channel

14. List of Contributors

16. Epithelial [Na.sup.+] channel mutants causing Liddle's syndrome retain ability to respond to aldosterone and vasopressin

17. Limit Dextrinosis

18. Lipoproteinosis

19. Lisch Epithelial Corneal Dystrophy

20. Livedo Telangiectatica

21. Lactase Nonpersistence

22. Livedo Vasculitis

23. Louis-Bar Syndrome

24. Lichen Planopilaris

25. Lenegre-Lev Syndrome

26. Lung Disease, Environmental

27. Linear IgA Disease

28. Lymphedema and Ptosis

29. Leigh Syndrome

30. Lymphoplasmacytic Lymphoma

31. Laënnec's Cirrhosis

32. Limb Girdle Muscular Dystrophy Type 2A

33. Laterality Abnormalities

34. Left Ventricular Enlargement

35. Limb Girdle Muscular Dystrophy, Autosomal Dominant Type 1C

36. Léri-Weill Dyschondrosteosis

37. Lymphedema-Cholestasis Syndrome

38. Léri-Weill Syndrome

39. Lamellar Ichthyosis

40. LGMD 2B

41. Langerhans Cell Granulomatosis

42. LGMD 1B

43. Left Bundle Branch Block

44. Lou Gehrig’s Disease

45. Lichen Sclerosus et Atrophicus

46. Labial Fusion

47. Lymphoproliferative Syndrome, X-linked

48. Contributors

49. Legg-Calvé-Perthes' Disease

50. Liver Failure, Acute

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