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4. Linkage of familial dysalbuminemic hyperthyroxinemia to the albumin gene in a large Amish kindred. Weiss RE; Sunthornthepvarakul T; Angkeow P; Marcus-Bagley D; Cox N; Alper CA; Refetoff S J Clin Endocrinol Metab; 1995 Jan; 80(1):116-21. PubMed ID: 7829599 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. A point mutation in the albumin gene in a Chinese patient with familial dysalbuminemic hyperthyroxinemia. Tang KT; Yang HJ; Choo KB; Lin HD; Fang SL; Braverman LE Eur J Endocrinol; 1999 Oct; 141(4):374-8. PubMed ID: 10526251 [TBL] [Abstract][Full Text] [Related]
7. Elevated thyroxine and free thyroxine in euthyroid patients: familial dysalbuminemic hyperthyroxinemia. Haas S S D J Med; 1990 Mar; 43(3):5-7. PubMed ID: 2109350 [TBL] [Abstract][Full Text] [Related]
8. [Familial dysalbuminemic hyperthyroxinemia in long-term amiodarone treated patients]. Sternad H; Eber B; Langsteger W; Prohaska R; Költringer P; Wawschinek O; Klein W; Eber O Acta Med Austriaca; 1994; 21(1):8-10. PubMed ID: 8017165 [TBL] [Abstract][Full Text] [Related]
9. An identical missense mutation in the albumin gene results in familial dysalbuminemic hyperthyroxinemia in 8 unrelated families. Sunthornthepvarakul T; Angkeow P; Weiss RE; Hayashi Y; Refetoff S Biochem Biophys Res Commun; 1994 Jul; 202(2):781-7. PubMed ID: 8048949 [TBL] [Abstract][Full Text] [Related]
10. Familial dysalbuminemic hyperthyroxinemia associated with primary thyroid disease. Young RA; Stoffer SS; Braverman LE Am J Med; 1987 Feb; 82(2):221-3. PubMed ID: 3812513 [TBL] [Abstract][Full Text] [Related]
12. Identification of a human serum albumin species associated with familial dysalbuminemic hyperthyroxinemia. Rushbrook JI; Becker E; Schussler GC; Divino CM J Clin Endocrinol Metab; 1995 Feb; 80(2):461-7. PubMed ID: 7852505 [TBL] [Abstract][Full Text] [Related]
13. A novel missense mutation in codon 218 of the albumin gene in a distinct phenotype of familial dysalbuminemic hyperthyroxinemia in a Japanese kindred. Wada N; Chiba H; Shimizu C; Kijima H; Kubo M; Koike T J Clin Endocrinol Metab; 1997 Oct; 82(10):3246-50. PubMed ID: 9329347 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Familial dysalbuminemic byperthyroxinemia may result in altered warfarin pharmacokinetics. Petersen CE; Ha CE; Harohalli K; Park DS; Bhagavan NV Chem Biol Interact; 2000 Feb; 124(3):161-72. PubMed ID: 10728776 [TBL] [Abstract][Full Text] [Related]
17. Mutations in a specific human serum albumin thyroxine binding site define the structural basis of familial dysalbuminemic hyperthyroxinemia. Petersen CE; Ha CE; Jameson DM; Bhagavan NV J Biol Chem; 1996 Aug; 271(32):19110-7. PubMed ID: 8702585 [TBL] [Abstract][Full Text] [Related]
18. Prevalence of familial dysalbuminemic hyperthyroxinemia in serum samples received for thyroid testing. Arevalo G Clin Chem; 1991 Aug; 37(8):1430-1. PubMed ID: 1868606 [TBL] [Abstract][Full Text] [Related]
19. A point mutation in the human serum albumin gene results in familial dysalbuminaemic hyperthyroxinaemia. Petersen CE; Scottolini AG; Cody LR; Mandel M; Reimer N; Bhagavan NV J Med Genet; 1994 May; 31(5):355-9. PubMed ID: 8064810 [TBL] [Abstract][Full Text] [Related]
20. Expression of a human serum albumin variant with high affinity for thyroxine. Petersen CE; Ha CE; Mandel M; Bhagavan NV Biochem Biophys Res Commun; 1995 Sep; 214(3):1121-9. PubMed ID: 7575519 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]