Similar articles for PMID: 8784093

Year	Number of Results
1979	2
1980	1
1982	5
1983	2
1984	1
1985	4
1986	4
1987	10
1988	11
1989	6
1990	11
1991	9
1992	10
1993	10
1994	12
1995	5
1996	5
1997	7
1998	2
1999	4
2000	7
2001	4
2002	5
2003	6
2004	2
2005	2
2006	2
2008	1
2009	1
2012	2
2013	6
2014	10
2015	3
2016	4
2017	8
2018	8
2019	8
2020	5
2021	1
2022	1
2023	3
2024	0

1

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. Refetoff S, et al. J Clin Endocrinol Metab. 1996 Sep;81(9):3335-40. doi: 10.1210/jcem.81.9.8784093. J Clin Endocrinol Metab. 1996. PMID: 8784093

2

[Thyroxine-binding proteins--familial euthyroid hyperthyroxinemia due to point mutations of transthyretin].

Hishinuma A, Mochizuki Y, Kasai K, Shimoda S. Hishinuma A, et al. Nihon Rinsho. 1994 Apr;52(4):886-9. Nihon Rinsho. 1994. PMID: 8196175 Review. Japanese.

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. Rosen HN, et al. J Clin Endocrinol Metab. 1993 Aug;77(2):370-4. doi: 10.1210/jcem.77.2.8345041. J Clin Endocrinol Metab. 1993. PMID: 8345041

4

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. Alves IL, et al. J Clin Endocrinol Metab. 1993 Aug;77(2):484-8. doi: 10.1210/jcem.77.2.8102146. J Clin Endocrinol Metab. 1993. PMID: 8102146

5

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. Moses AC, et al. J Clin Invest. 1990 Dec;86(6):2025-33. doi: 10.1172/JCI114938. J Clin Invest. 1990. PMID: 1979335 Free PMC article.

6

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. Lalloz MR, et al. J Clin Endocrinol Metab. 1987 Feb;64(2):346-52. doi: 10.1210/jcem-64-2-346. J Clin Endocrinol Metab. 1987. PMID: 3098776

7

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. Rosen HN, et al. Endocrinology. 1994 Jan;134(1):27-34. doi: 10.1210/endo.134.1.8275943. Endocrinology. 1994. PMID: 8275943

8

Euthyroid hyperthyroxinemia due to familial excess of thyroxine-binding globulin.

Tucker WS Jr. Tucker WS Jr. South Med J. 1989 Mar;82(3):368-71. doi: 10.1097/00007611-198903000-00022. South Med J. 1989. PMID: 2493680

9

Etiology and outcome of non-estrogen associated hyperthyroxinemia in euthyroid patients at the San Juan City Hospital.

Alegre M, Meléndez EG, Colón G. Alegre M, et al. Bol Asoc Med P R. 1996 Jan-Mar;88(1-3):12-5. Bol Asoc Med P R. 1996. PMID: 8885441

10

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. Weiss RE, et al. J Clin Endocrinol Metab. 1995 Jan;80(1):116-21. doi: 10.1210/jcem.80.1.7829599. J Clin Endocrinol Metab. 1995. PMID: 7829599

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