These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
3. SEVEN FAMILIAL DYSALBUMINEMIC HYPERTHYROXINEMIA CASES IN THREE UNRELATED JAPANESE FAMILIES AND HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY ANALYSIS OF THE THYROXINE BINDING PROFILE. Nagano H; Nakagawa Y; Ishikawa N; Watanabe H; Miyabayashi Y; Nakayama A; Fujimoto M; Komai E; Shiga A; Tamura A; Kono T; Takiguchi T; Higuchi S; Sakuma I; Hashimoto N; Suzuki S; Koide H; Yokote K; Tanaka T Endocr Pract; 2017 Nov; 23(11):1325-1332. PubMed ID: 28816534 [TBL] [Abstract][Full Text] [Related]
4. Homozygous Mutation in Human Serum Albumin and Its Implication on Thyroid Tests. Mimoto MS; Karaca A; Scherberg N; Dumitrescu AM; Refetoff S Thyroid; 2018 Jun; 28(6):811-814. PubMed ID: 29676214 [TBL] [Abstract][Full Text] [Related]
5. A novel mutation in the Albumin gene (R218S) causing familial dysalbuminemic hyperthyroxinemia in a family of Bangladeshi extraction. Greenberg SM; Ferrara AM; Nicholas ES; Dumitrescu AM; Cody V; Weiss RE; Refetoff S Thyroid; 2014 Jun; 24(6):945-50. PubMed ID: 24494774 [TBL] [Abstract][Full Text] [Related]
6. Artifactually elevated serum-free thyroxine levels measured by equilibrium dialysis in a pregnant woman with familial dysalbuminemic hyperthyroxinemia. Hoshikawa S; Mori K; Kaise N; Nakagawa Y; Ito S; Yoshida K Thyroid; 2004 Feb; 14(2):155-60. PubMed ID: 15068631 [TBL] [Abstract][Full Text] [Related]
7. First Report of Familial Dysalbuminemic Hyperthyroxinemia With an ALB Variant. Cho YY; Song JS; Park HD; Kim YN; Kim HI; Kim TH; Chung JH; Ki CS; Kim SW Ann Lab Med; 2017 Jan; 37(1):63-65. PubMed ID: 27834068 [TBL] [Abstract][Full Text] [Related]
8. Familial dysalbuminemic hyperthyroxinemia (FDH) due to Arg242 His variant in Turkkahraman D; Gullu M; Tekin S; Kalkan T J Pediatr Endocrinol Metab; 2024 Jun; 37(6):532-535. PubMed ID: 38736368 [TBL] [Abstract][Full Text] [Related]
9. 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 J Clin Endocrinol Metab; 2000 Aug; 85(8):2786-92. PubMed ID: 10946882 [TBL] [Abstract][Full Text] [Related]
10. Familial Dysalbuminemic Hyperthyroxinemia in a Japanese Man Caused by a Point Albumin Gene Mutation (R218P). Osaki Y; Hayashi Y; Nakagawa Y; Yoshida K; Ozaki H; Fukazawa H Jpn Clin Med; 2016; 7():9-13. PubMed ID: 27081329 [TBL] [Abstract][Full Text] [Related]
11. Free Thyroxine Concentrations in Sera of Individuals with Familial Dysalbuminemic Hyperthyroxinemia: A Comparison of Three Methods of Measurement. Refetoff S; Scherberg NH; Yuan C; Wu W; Wu Z; McPhaul MJ Thyroid; 2020 Jan; 30(1):37-41. PubMed ID: 31822224 [No Abstract] [Full Text] [Related]
12. Familial Dysalbuminemic Hyperthyroxinemia (FDH), Albumin Gene Variant (R218S), and Risk of Miscarriages in Offspring. Lai S; Gopalakrishnan G; Li J; Liu X; Chen Y; Wen Y; Zhang S; Huang B; Phornphutkul C; Liu S; Kuang J Am J Med Sci; 2020 Nov; 360(5):566-574. PubMed ID: 32665066 [TBL] [Abstract][Full Text] [Related]
15. Clinical characteristics of familial dysalbuminemic hyperthyroxinemia in Chinese patients and comparison of free thyroxine in three immunoassay methods. Zhao L; Zhou Y; Huang F; He X; Mei G; Wang S; Zhao Y Front Endocrinol (Lausanne); 2023; 14():1102777. PubMed ID: 36864842 [TBL] [Abstract][Full Text] [Related]
16. A case of familial dysalbuminemic hyperthyroxinemia (FDH) in Japan: FDH as a possible differential diagnosis of syndrome of inappropriate secretion of thyroid-stimulating hormone (SITSH). Kobayashi S; Yoshimura Noh J; Shimizu T; Sato T; Kurihara I; Sugino K; Itoh H; Ito K Endocr J; 2017 Feb; 64(2):207-212. PubMed ID: 27904073 [TBL] [Abstract][Full Text] [Related]
17. Familial Dysalbuminemic Hyperthyroxinemia that was Inappropriately Treated with Thiamazole Due to Pseudo-thyrotoxic Symptoms. Fukaishi T; Sekiguchi Y; Hara Y Intern Med; 2017 Aug; 56(16):2175-2180. PubMed ID: 28781323 [TBL] [Abstract][Full Text] [Related]
18. Structural investigations of a new familial dysalbuminemic hyperthyroxinemia genotype. Petersen CE; Ha CE; Harohalli K; Park DS; Feix JB; Isozaki O; Bhagavan NV Clin Chem; 1999 Aug; 45(8 Pt 1):1248-54. PubMed ID: 10430791 [TBL] [Abstract][Full Text] [Related]
19. [Familial hyperthyroxinemia with dysalbuminemia: screening of 21,000 patients at the occasion of thyroid evaluation]. Sapin R; Gasser F; Chambron J Pathol Biol (Paris); 1989 Sep; 37(7):785-9. PubMed ID: 2631028 [TBL] [Abstract][Full Text] [Related]
20. Familial dysalbuminemic hyperthyroxinemia: a rare example of albumin polymorphism and its rapid molecular diagnosis. AvRuskin TW; Juan CS; Weiss RE J Pediatr Endocrinol Metab; 2002 Jun; 15(6):801-7. PubMed ID: 12099390 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]