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Orvosi Hetilap|February 13, 2018
[Steroid 21-hydroxylase deficiency, the most frequent cause of congenital adrenal hyperplasia]Márton Doleschall, Dóra Török, Katalin Mészáros, et al.
Orvosi Hetilap|November 3, 2024
[Diagnosis and treatment of medullary thyroid cancer in four Hungarian university centers (2000-2023)]Zsuzsanna Réti, Judit Tőke, Réka Balla, et al.
Endocrine|May 3, 2019
True MEN1 or phenocopy? Evidence for geno-phenotypic correlations in MEN1 syndromeAnnamária Kövesdi, Miklós Tóth, Henriett Butz, et al.
European Journal of Endocrinology|September 18, 2025
Prospective study of metyrapone in endogenous Cushing's syndrome (PROMPT)Lynnette K Nieman, Marco Boscaro, Carla Scaroni, et al.
European Journal of Endocrinology|June 15, 2026
Prevalence of somatic SF3B1R625H mutation in lactotroph tumours from a multi-centric cohort: A digital PCR based studyAshutosh Rai, Sayka Barry, Federica Mangili, et al.
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