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1. List of Contributors

5. Hyperphosphatemic tumoral calcinosis caused by FGF23 compound heterozygous mutations: what are the therapeutic options for a better control of phosphatemia?

6. Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement

7. Parathyroid hormone receptors in GtoPdb v.2023.1

9. List of Contributors

14. Practice patterns for chronic hypoparathyroidism: data from patients and physicians in France

15. Practice patterns for chronic hypoparathyroidism: data from patients and physicians in France

16. Familial Hypocalciuric Hypercalcemia Types 1 and 3 and Primary Hyperparathyroidism: Similarities and Differences

20. Contributors

21. Parathyroid hormone receptors in GtoPdb v.2021.3

29. 'Isolated' Amelogenesis Imperfecta Associated with DLX3 Mutation: A Clinical Case

30. List of Contributors

32. Simultaneous Hyper- and Hypomethylation at Imprinted Loci in a Subset of Patients with GNAS Epimutations Underlies a Complex and Different Mechanism of Multilocus Methylation Defect in Pseudohypoparathyroidism Type 1b

36. PRKAR1A and PDE4D Mutations Cause Acrodysostosis but Two Distinct Syndromes with or without GPCR-Signaling Hormone Resistance

38. Nephrolithiasis and osteoporosis associated with hypophosphatemia caused by mutations in the type 2a sodium-phosphate cotransporter

39. Central Type of Neurofibromatosis

40. Cardiomyopathies

41. Pancreas Annulare

42. Pulmonary Valve Incompetence

43. Multiple Epiphyseal Dysplasia

44. Precocious Puberty

45. Map-Dot-Fingerprint-Bleb Dystrophy

46. Cavernous Haemangioma

47. Cardiac Infarction

48. Mortimer’s Malady

49. Cardiomyopathy, Dilated

50. Protein S Deficiency

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