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Cited by CrossRef (12)

  1. C. Sager, M. López-Ruano, S. Jiménez-Blanco, A. Justel-Enríquez. Indicaciones e interpretación de pruebas complementarias analíticas en la patología tiroidea. Medicine - Programa de Formación Médica Continuada Acreditado 2024;14:835
    https://doi.org/10.1016/j.med.2024.07.008
  2. Qian Sun, Lívia Avallone, Brian Stolze, Katherine A. Araque, Yesim Özarda, Jacqueline Jonklaas, Toral Parikh, Kerry Welsh, Likhona Masika, Steven J. Soldin. Demonstration of reciprocal diurnal variation in human serum T3 and rT3 concentration demonstrated by mass spectrometric analysis and establishment of thyroid hormone reference intervals. Therapeutic Advances in Endocrinology 2020;11
    https://doi.org/10.1177/2042018820922688
  3. Linlin Zhao, Yingying Zhou, Fengjiao Huang, Xiaoyang He, Guili Mei, Shoujun Wang, Yanyan Zhao. Clinical characteristics of familial dysalbuminemic hyperthyroxinemia in Chinese patients and comparison of free thyroxine in three immunoassay methods. Front. Endocrinol. 2023;14
    https://doi.org/10.3389/fendo.2023.1102777
  4. Agata Maria Kalicka. Diagnosis of Graves’ disease – laboratory tests and possible difficulties in interpretation. diagn lab 2019;55:121
    https://doi.org/10.5604/01.3001.0013.7454
  5. Ekaterina I. Kim, Diana А. Dimitrova, Diana A. Dimitrova, Nino N. Katamadze, Tamara S. Dzantieva. Endogenous and exogenous interferences in thyroid function immunoassays. Clin Exp Thyroid 2021;16:16
    https://doi.org/10.14341/ket12698
  6. Da-Wei Chen, Zuo Du, Chun-Ze Zhang, Wei-Hua Zhang, Yun-Feng Cao, Hong-Zhi Sun, Zhi-Tu Zhu, Kun Yang, Yong-Zhe Liu, Ze-Wei Zhao, Zhi-Wei Fu, Wen-Qing Gu, Yang Yu, Zhong-Ze Fang. The inhibition of UDP-glucuronosyltransferases (UGTs) by tetraiodothyronine (T4) and triiodothyronine (T3). Xenobiotica 2018;48:250
    https://doi.org/10.1080/00498254.2017.1304593
  7. Shuiqing Lai, Geetha Gopalakrishnan, Jie Li, Xin Liu, Yuancheng Chen, Yuqiong Wen, Shuting Zhang, Bizhu Huang, Chanika Phornphutkul, Simin Liu, Jian Kuang. Familial Dysalbuminemic Hyperthyroxinemia (FDH), Albumin Gene Variant (R218S), and Risk of Miscarriages in Offspring. The American Journal of the Medical Sciences 2020;360:566
    https://doi.org/10.1016/j.amjms.2020.05.035
  8. Ulrich Kragh-Hansen, Monica Galliano, Lorenzo Minchiotti. Clinical, Genetic, and Protein Structural Aspects of Familial Dysalbuminemic Hyperthyroxinemia and Hypertriiodothyroninemia. Front. Endocrinol. 2017;8
    https://doi.org/10.3389/fendo.2017.00297
  9. Shui-Boon Soh, Tar-Choon Aw. Laboratory Testing in Thyroid Conditions - Pitfalls and Clinical Utility. Ann Lab Med 2019;39:3
    https://doi.org/10.3343/alm.2019.39.1.3
  10. Julien Favresse, Maria-Cristina Burlacu, Dominique Maiter, Damien Gruson. Interferences With Thyroid Function Immunoassays: Clinical Implications and Detection Algorithm. 2018;39:830
    https://doi.org/10.1210/er.2018-00119
  11. Yoon Young Cho. Familial Dysalbuminemic Hyperthyroxinemia by Albumin Gene Variant (R242H) in a 19-Year-Old Male: A Case Report. Soonchunhyang Med Sci 2023;29:77
    https://doi.org/10.15746/sms.23.018
  12. Ashleigh Brown, Paul Hofman, Bobby Li, Campbell Heron, Natasha Heather. A Positive Newborn Screen for Congenital Hypothyroidism in a Clinically Euthyroid Neonate—Avoiding Unnecessary Treatment. IJNS 2023;9:16
    https://doi.org/10.3390/ijns9020016