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3. Diagnostic Utility of Exome Sequencing Among Israeli Children With Kidney Failure

4. Glomerular involvement in children with H syndrome

5. Dominant PAX2 mutations may cause steroid-resistant nephrotic syndrome and FSGS in children

8. X-linked C1GALT1C1mutation causes atypical hemolytic uremic syndrome

9. Hypoparathyroidism-retardation-dysmorphism syndrome—Clinical insights from a large longitudinal cohort in a single medical center

10. FC035: Exome Sequencing of the Israeli Dialysis-Treated Pediatric Population Reveals Monogenic Etiology in ∼44% of Cases

14. Hb Bart’s Hydrops Fetalis

15. Hippocratic Fingers

16. Hyperekplexia, Hereditary

17. Hereditary Hearing Impairment

18. Hematochezia

19. Holt-Oram Syndrome

20. Hypertension and Obesity

21. Hypokalemic Alkalosis with Hypercalciuria and Deafness

22. Hereditary Neuropathy with Liability to Pressure Palsies

23. Hereditary Inclusion Body Myopathy 3

24. Heat Stroke

25. Hypercatabolic Protein-losing Enteropathy

26. Hemolytic Anemia

27. Hereditary Nonhemolytic Unconjugated Hyperbilirubinemia

28. Hepatitis, Granulomatous

29. HPV-associated Laryngeal Cancer

30. Haim-Munk Syndrome

31. Hearing Impairment, Syndromal

32. Hyperthyroidism, Sporadic Non-autoimmune

33. Heredopathia Atactica Polyneuritiformis

34. Hereditary Nonautoimmune Autosomal Dominant Toxic Thyroid Hyperplasia

35. Hartnup Disorder

36. Hypocalciuric Hypercalcemia, Familial

37. Haws Type Brachydactyly

38. Hypomagnesemia with Secondary Hypocalcemia

39. Hepatic Triglyceride Lipase Deficiency

40. Hypertension, Idiopathic and Familial Pulmonary Arterial

41. Hyperostose en Coulée

42. Hereditary Conjugated Hyperbilirubinemia

43. Hyperkalemic Renal Tubular Acidosis

44. Hypothyroidism, Nongoitrous Congenital

45. Hypoxanthine-Guanine Phosphoribosyl Transferase Deficiency

46. Hypophosphatemia, X-linked

47. Hypervitaminosis E

48. Hypophosphatemia with Renal Phosphate Loss

49. Homocysteine: Plasma Levels and Genetic Basis

50. Hyperoxalurias, Primary

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