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Page 1
Inherited defects of thyroxine-binding proteins.
Pappa T, Ferrara AM, Refetoff S. Pappa T, et al. Best Pract Res Clin Endocrinol Metab. 2015 Oct;29(5):735-47. doi: 10.1016/j.beem.2015.09.002. Epub 2015 Sep 30. Best Pract Res Clin Endocrinol Metab. 2015. PMID: 26522458 Free PMC article. Review.
Familial dysalbuminemic hyperthyroxinemia and thyroid hormone autoantibodies: interference in current free thyroid hormone assays.
Sapin R, Gasser F, Schlienger JL. Sapin R, et al. Horm Res. 1996;45(3-5):139-41. doi: 10.1159/000184776. Horm Res. 1996. PMID: 8964572 Review.
The interference of familial dysalbuminemic hyperthyroxinemia (FDH), antithyroxine (anti-T4) or antitriiodothyronine (anti-T3) antibodies in serum free T4 (FT4) or free T3 (FT3) assays depends on the assay method: two-step immunoextraction, one-step labelled …
The interference of familial dysalbuminemic hyperthyroxinemia (FDH), antithyroxine (anti-T4) or antitriiodothyronine (a …
Familial dysalbuminemic hyperthyroxinemia in a Swiss family caused by a mutant albumin (R218P) shows an apparent discrepancy between serum concentration and affinity for thyroxine.
Pannain S, Feldman M, Eiholzer U, Weiss RE, Scherberg NH, Refetoff S. Pannain S, et al. J Clin Endocrinol Metab. 2000 Aug;85(8):2786-92. doi: 10.1210/jcem.85.8.6746. J Clin Endocrinol Metab. 2000. PMID: 10946882 Review.
Familial dysalbuminemic hyperthyroxinemia (FDH), is the most common cause of inherited increase in serum total T4 (TT4) in the Caucasian population. ...
Familial dysalbuminemic hyperthyroxinemia (FDH), is the most common cause of inherited increase in serum total T4 (TT4)
An overview of thyroid function tests in subjects with resistance to thyroid hormone and related disorders.
Tagami T. Tagami T. Endocr J. 2021 May 28;68(5):509-517. doi: 10.1507/endocrj.EJ21-0059. Epub 2021 May 6. Endocr J. 2021. PMID: 33827995 Free article. Review.
The differential diagnoses of RTHbeta include TSH-producing pituitary adenoma (TSHoma) and familial dysalbuminemic hyperthyroxinemia (FDH), which also present SITSH. ...
The differential diagnoses of RTHbeta include TSH-producing pituitary adenoma (TSHoma) and familial dysalbuminemic hyperthy
Variations in thyroid hormone transport proteins and their clinical implications.
Bartalena L, Robbins J. Bartalena L, et al. Thyroid. 1992 Fall;2(3):237-45. doi: 10.1089/thy.1992.2.237. Thyroid. 1992. PMID: 1422238 Review.
Increased serum total thyroid hormone levels are found in subjects with TBG excess, familial dysalbuminemic hyperthyroxinemia, and transthyretin-associated hyperthyroxinemia. ...
Increased serum total thyroid hormone levels are found in subjects with TBG excess, familial dysalbuminemic hyperthyroxinem
Measurement of serum free thyroid hormone concentrations: an essential tool for the diagnosis of thyroid dysfunction.
Bartalena L, Bogazzi F, Brogioni S, Burelli A, Scarcello G, Martino E. Bartalena L, et al. Horm Res. 1996;45(3-5):142-7. doi: 10.1159/000184777. Horm Res. 1996. PMID: 8964573 Review.
Thus, increased serum total T4 (TT4) and, in many instances, T3 (TT3) concentrations are encountered in euthyroid subjects with TBG excess, familial dysalbuminemic hyperthyroxinemia and transthyretin-associated hyperthyroxinemia, while decreased serum …
Thus, increased serum total T4 (TT4) and, in many instances, T3 (TT3) concentrations are encountered in euthyroid subjects with TBG excess, …
[Thyroxine (T4) and tri-iodothyronine (T3) determinations: techniques and value in the assessment of thyroid function].
Sapin R, Schlienger JL. Sapin R, et al. Ann Biol Clin (Paris). 2003 Jul-Aug;61(4):411-20. Ann Biol Clin (Paris). 2003. PMID: 12915350 Free article. Review. French.
Free hormone measurement remains technically demanding, especially in sera from severe non-thyroid ill patients with low serum thyroxine binding capacity. Interference from anti-thyroid hormone antibodies and familial dysalbuminemic hyperthyroxinemia depends …
Free hormone measurement remains technically demanding, especially in sera from severe non-thyroid ill patients with low serum thyroxine bin …
Bisalbuminemia from a clinical chemist's viewpoint: a case report and review of the recent literature.
Faviou E, Nounopoulos C, Dionyssiou-Asteriou A. Faviou E, et al. Minerva Med. 2006 Jun;97(3):287-93. Minerva Med. 2006. PMID: 16855523 Review.
Until now, the only disorders which have been directly linked with the presence of congenital bisalbuminemia are familial dysalbuminemic hyperthyroxinemia (Arg218AEHis and Arg218AE Pro mutations) and hypertriiodothyroninemia (Leu66AEPro mutation), while acqui …
Until now, the only disorders which have been directly linked with the presence of congenital bisalbuminemia are familial dysalbum
11 results