Edit Gláz

From Wikipedia, the free encyclopedia

Edit Gláz was a Hungarian endocrinologist[1] and a Professor of Endocrinology.[2] She was born in Budapest on September 8, 1926.[3] Her work included research on salivary cortisol[4][5] as well as germline VHL mutations in Hungarian families with von Hippel-Lindau disease.[6] She was awarded the Silver degree of the Order of Merit in 1986 and the Semmelweis Medal in 1995.[3] She died on December 20, 2020[3]

References[edit]

  1. ^ "Dr. Gláz Edit, endokrinológus". foglaljorvost.hu (in Hungarian). Retrieved 2023-12-04.
  2. ^ European Society of Endocrinology (2019). "Women in endocrinology" (PDF). ESE News. p. 10.
  3. ^ a b c "Elhunyt dr. Gláz Edit". semmelweis.hu (in Hungarian). 2020-12-22. Retrieved 2023-12-04.
  4. ^ Beko, Gabriella; Varga, Ibolya; Glaz, Edit; Sereg, Marta; Feldman, Karolina; Toth, Miklós; Racz, Karoly; Patocs, Attila (2010-03-02). "Cutoff values of midnight salivary cortisol for the diagnosis of overt hypercortisolism are highly influenced by methods". Clinica Chimica Acta. 411 (5): 364–367. doi:10.1016/j.cca.2009.11.033. ISSN 0009-8981. PMID 19968981.
  5. ^ Szappanos, Agnes; Patocs, Attila; Toke, Judit; Sereg, Marta; Futo, Laszlo; Kende, Zoltan; Varga, Ibolya; Glaz, Edit; Racz, Karoly; Toth, Miklos (2008-05-01). "Glucocorticoid receptor gene polymorphisms in patients with Cushing". Endocrine Abstracts. 16. ISSN 1470-3947.
  6. ^ Gergics, Peter; Patocs, Attila; Toth, Miklos; Igaz, Peter; Szucs, Nikolette; Liko, Istvan; Fazakas, Ferenc; Szabo, Istvan; Kovacs, Balazs; Glaz, Edit; Racz, Karoly (September 2009). "Germline VHL gene mutations in Hungarian families with von Hippel-Lindau disease and patients with apparently sporadic unilateral pheochromocytomas". European Journal of Endocrinology. 161 (3): 495–502. doi:10.1530/EJE-09-0399. ISSN 1479-683X. PMID 19574279.