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2. Presenile forms of Alzheimer’s disease in 2006

5. Myopathy with hexagonally cross-linked crystalloid inclusions: Delineation of a clinico-pathological entity

10. Fulminant Hepatic Failure

11. Female Infertility

12. Fat Necrosis

13. Folic Acid Deficiency

14. Familial CD8 Deficiency

15. Fanconi Syndrome

16. FIX

17. Fatty Liver Disease, Nonalcoholic

18. Fibrinogen Deficiencies Type II

19. Familial Protein Intolerance

20. Fasciitis, Eosinophilic

21. François-Neetens Speckled Corneal Dystrophy

22. Focal Mesangial Proliferative Glomerulonephritis

23. Farmer’s Lung Disease

24. FHBL due to Defective PCSK9

25. Fronto-Temporal Dementia

26. Fiber Type Disproportion, Congenital

27. Familial Periodic Paralyses

28. Female Pseudohermaphroditism

29. Familial Benign Hypocalciuric Hypercalcemia

30. Fetal Varicella Syndrome

31. Fabry Disease

32. Fuchs Endothelial Corneal Dystrophy

33. Familial Periodic Ataxia

34. Familial Hemiplegic Migraine

35. Fetal Face Syndrome

36. Familial Mediterranean Fever

37. Familial Hematuria

38. Fatty Liver/Fatty Liver Disease

39. Flea-Bite Dermatitis

40. Fibrinogen: Quantitative Mutations

41. Familial Defective ApoB-100

42. Fibrinogen: Qualitative Disorders

43. Familial Adult Myoclonic Epilepsy

44. Familial Benign Chronic Pemphigus

45. Familial Incomplete Male Pseudohermaphroditism Type I

46. Fragile X Syndrome A

47. Facioscapulohumeral Muscular Dystrophy

48. Familial Isolated Deficiency of Vitamin E

49. Fanconi Renotubular Syndrome

50. FSH Beta Subunit Deficiency

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