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Journal Abstract Search
128 related items for PubMed ID: 8196175
1. [Thyroxine-binding proteins--familial euthyroid hyperthyroxinemia due to point mutations of transthyretin]. Hishinuma A, Mochizuki Y, Kasai K, Shimoda S. Nihon Rinsho; 1994 Apr; 52(4):886-9. PubMed ID: 8196175 [Abstract] [Full Text] [Related]
2. A new family with hyperthyroxinemia caused by transthyretin Val109 misdiagnosed as thyrotoxicosis and resistance to thyroid hormone--a clinical research center study. Refetoff S, Marinov VS, Tunca H, Byrne MM, Sunthornthepvarakul T, Weiss RE. J Clin Endocrinol Metab; 1996 Sep; 81(9):3335-40. PubMed ID: 8784093 [Abstract] [Full Text] [Related]
3. Thyroxine interactions with transthyretin: a comparison of 10 different naturally occurring human transthyretin variants. Rosen HN, Moses AC, Murrell JR, Liepnieks JJ, Benson MD. J Clin Endocrinol Metab; 1993 Aug; 77(2):370-4. PubMed ID: 8345041 [Abstract] [Full Text] [Related]
4. A point mutation in transthyretin increases affinity for thyroxine and produces euthyroid hyperthyroxinemia. Moses AC, Rosen HN, Moller DE, Tsuzaki S, Haddow JE, Lawlor J, Liepnieks JJ, Nichols WC, Benson MD. J Clin Invest; 1990 Dec; 86(6):2025-33. PubMed ID: 1979335 [Abstract] [Full Text] [Related]
5. Dysprealbuminemic hyperthyroxinemia in a patient with hyperthyroid graves disease. Cameron SJ, Hagedorn JC, Sokoll LJ, Caturegli P, Ladenson PW. Clin Chem; 2005 Jun; 51(6):1065-9. PubMed ID: 15833783 [Abstract] [Full Text] [Related]
6. Thyroxine binding in a TTR Met 119 kindred. Alves IL, Divino CM, Schussler GC, Altland K, Almeida MR, Palha JA, Coelho T, Costa PP, Saraiva MJ. J Clin Endocrinol Metab; 1993 Aug; 77(2):484-8. PubMed ID: 8102146 [Abstract] [Full Text] [Related]
7. Etiology and outcome of non-estrogen associated hyperthyroxinemia in euthyroid patients at the San Juan City Hospital. Alegre M, Meléndez EG, Colón G. Bol Asoc Med P R; 1996 Aug; 88(1-3):12-5. PubMed ID: 8885441 [Abstract] [Full Text] [Related]
8. Transthyretin mutations in hyperthyroxinemia and amyloid diseases. Saraiva MJ. Hum Mutat; 2001 Jun; 17(6):493-503. PubMed ID: 11385707 [Abstract] [Full Text] [Related]
9. Novel mutation p.A64D in the Serpina7 gene as a cause of partial thyroxine-binding globulin deficiency associated with increases affinity in transthyretin by a known p.A109T mutation in the TTR gene. Sklate RT, Olcese MC, Maccallini GC, Sarmiento RG, Targovnik HM, Rivolta CM. Horm Metab Res; 2014 Feb; 46(2):100-8. PubMed ID: 24356794 [Abstract] [Full Text] [Related]
10. Production and functional analysis of normal and variant recombinant human transthyretin proteins. Murrell JR, Schoner RG, Liepnieks JJ, Rosen HN, Moses AC, Benson MD. J Biol Chem; 1992 Aug 15; 267(23):16595-600. PubMed ID: 1644839 [Abstract] [Full Text] [Related]
11. Hyperthyroxinemia due to the coexistence of two raised affinity thyroxine-binding proteins (albumin and prealbumin) in one family. Lalloz MR, Byfield PG, Goel KM, Loudon MM, Thomson JA, Himsworth RL. J Clin Endocrinol Metab; 1987 Feb 15; 64(2):346-52. PubMed ID: 3098776 [Abstract] [Full Text] [Related]
12. Elevated thyroxine levels in a euthyroid patient. A search for the cause of euthyroid hyperthyroxinemia. Uy HL, Reasner CA. Postgrad Med; 1994 Oct 15; 96(5):195-202. PubMed ID: 7937417 [Abstract] [Full Text] [Related]
13. Threonine for alanine substitution at position 109 of transthyretin differentially alters human transthyretin's affinity for iodothyronines. Rosen HN, Murrell JR, Liepnieks JJ, Benson MD, Cody V, Moses AC. Endocrinology; 1994 Jan 15; 134(1):27-34. PubMed ID: 8275943 [Abstract] [Full Text] [Related]
14. Transient prealbumin-associated hyperthyroxinemia in TSH-producing pituitary adenoma. Lind P, Langsteger W, Költringer P, Wakonig P, Eber B, Mokry M, Beham A, Eber O. Nuklearmedizin; 1990 Feb 15; 29(1):40-3. PubMed ID: 2108434 [Abstract] [Full Text] [Related]
15. Familial euthyroid hyperthyroxinemia resulting from increased thyroxine binding to thyroxine-binding prealbumin. Moses AC, Lawlor J, Haddow J, Jackson IM. N Engl J Med; 1982 Apr 22; 306(16):966-9. PubMed ID: 6801514 [No Abstract] [Full Text] [Related]
16. Specific methods to identify plasma binding abnormalities in euthyroid hyperthyroxinemia. Stockigt JR, Dyer SA, Mohr VS, White EL, Barlow JW. J Clin Endocrinol Metab; 1986 Jan 22; 62(1):230-3. PubMed ID: 3079602 [Abstract] [Full Text] [Related]
17. Thyroxine binding to transthyretin Met 119. Comparative studies of different heterozygotic carriers and structural analysis. Almeida MR, Damas AM, Lans MC, Brouwer A, Saraiva MJ. Endocrine; 1997 Jun 22; 6(3):309-15. PubMed ID: 9368688 [Abstract] [Full Text] [Related]
18. Thyroxine binding by human transthyretin variants: mutations at position 119, but not position 54, increase thyroxine binding affinity. Curtis AJ, Scrimshaw BJ, Topliss DJ, Stockigt JR, George PM, Barlow JW. J Clin Endocrinol Metab; 1994 Feb 22; 78(2):459-62. PubMed ID: 7906282 [Abstract] [Full Text] [Related]
19. Change in structure of the N-terminal region of transthyretin produces change in affinity of transthyretin to T4 and T3. Prapunpoj P, Leelawatwatana L, Schreiber G, Richardson SJ. FEBS J; 2006 Sep 22; 273(17):4013-23. PubMed ID: 16879610 [Abstract] [Full Text] [Related]
20. Elevated thyroxine and free thyroxine in euthyroid patients: familial dysalbuminemic hyperthyroxinemia. Haas S. S D J Med; 1990 Mar 22; 43(3):5-7. PubMed ID: 2109350 [Abstract] [Full Text] [Related] Page: [Next] [New Search]