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11. IGSF1 mutations are the most frequent genetic aetiology of thyrotropin deficiency. Issue 6 (3rd November 2022)

12. In vitro impact of pegvisomant on growth hormone-secreting pituitary adenoma cells. Issue 7 (July 2016)

13. International initiative for a curated SDHB variant database improving the diagnosis of hereditary paraganglioma and pheochromocytoma. Issue 8 (27th August 2021)

16. Looking beyond the thyroid: advances in the understanding of pheochromocytoma and hyperparathyroidism phenotypes in MEN2 and of non-MEN2 familial forms. Issue 2 (February 2018)

17. MECHANISMS IN ENDOCRINOLOGY: An update in the genetic aetiologies of combined pituitary hormone deficiency. Issue 6 (June 2016)

18. Metabolomics signatures of a subset of RET variants according to their oncogenic risk level. Issue 3 (March 2019)

19. Multiple endocrine neoplasia type 1 caused by mosaic mutation: clinical follow-up and genetic counseling?. Issue 1 (24th May 2022)

20. Primary hyperparathyroidism as first manifestation in multiple endocrine neoplasia type 2A: an international multicenter study. Issue 6 (June 2020)