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2. Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes

3. Inherited human IRAK-1 deficiency selectively impairs TLR signaling in fibroblasts

6. Inversion Chromosomes

9. Acceptance of COVID-19 and Influenza Vaccine Co-Administration: Insights from a Representative Italian Survey

10. Supplement to: PRKACB and Carney Complex.

11. Loss-of-Function FANCL Mutations Associate with Severe Fanconi Anemia Overlapping the VACTERL Association

16. PRKACB and Carney Complex

17. Blanchard e Summers: rivoluzione o conservazione?

20. Reciprocal translocations: a trap for cytogenetists?

21. Isolated FSH Deficiency

22. Insulin Producing Tumor

23. Inclusion Body Myopathy, Hereditary

24. IHES

25. Intercellular IgA Dermatosis

26. Idiopathic Neuromyotonia

27. Incontinentia Pigmenti

28. Intestinal Lipodystrophy

29. Iodine Deficiency and Excess

30. Infertility, Immune-mediated

31. Inherited Peripheral Neuropathies

32. Idiopathic Dilated Cardiomyopathy

33. IgA Herpetiform Pemphigus

34. Infectious Arthritis

35. Idiopathic Parkinson Syndrome

36. Intrahepatic Jaundice

37. Idiopathic Pulmonary Hemosiderosis

38. Ichthyosis Congenital

39. Isosexual Precocious Puberty

40. Idiopathic Pulmonary Fibrosis

41. IDDM-secretory Diarrhea Syndrome

42. Idiopathic Orthostatic Hypotension

43. Iodine-related Disease States

44. Idiopathic Cerebellar Ataxia

45. Indirect Inguinal Hernia

46. Isolated Pituitary Hormone Deficiency

47. IgA Bullous Pemphigoid

48. Intermediate SMA Type II

49. Immune-mediated Infertility

50. Intra-adrenal Paraganglioma

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