Euthyroid hyperthyroxinemia: relevance of albumin and transthyretin genetic variations in a single centre experience
After exclusion of secondary causes, genetic variation in thyroid hormones transport proteins is a common cause of EH.
Authors
- Martina Montagnana (ORCID: https://orcid.org/0000-0001-8999-0001)
- Beth Susi
- Alfonso Massimiliano Ferrara (ORCID: https://orcid.org/0000-0001-5835-1709)
- Cristina Clausi
- Annalisa Stefani (ORCID: https://orcid.org/0000-0002-8071-0285)
- Simona Croitoru
- Ilaria Piva (ORCID: https://orcid.org/0009-0005-1473-6363)
- Monica Mion (ORCID: https://orcid.org/0000-0003-2468-7268)
- Caterina Mian (ORCID: https://orcid.org/0000-0003-1698-2902)
- Bertazza Loris
- Ruggeri Edoardo
Institutions
- University of Padua (IT)
- Istituto Oncologico Veneto (IT)
Publication Details
- Journal
- Clinica Chimica Acta
- Published
- 2025-05-09
- DOI
- https://doi.org/10.1016/j.cca.2025.120354
- Citations
- 1
- Primary Topic
- Erythrocyte Function and Pathophysiology
- Type
- article
- Field-Weighted Citation Impact
- 1.16