Page last updated: 2024-11-08

triiodothyronine and Hyperthyroxinemia

triiodothyronine has been researched along with Hyperthyroxinemia in 45 studies

Triiodothyronine: A T3 thyroid hormone normally synthesized and secreted by the thyroid gland in much smaller quantities than thyroxine (T4). Most T3 is derived from peripheral monodeiodination of T4 at the 5' position of the outer ring of the iodothyronine nucleus. The hormone finally delivered and used by the tissues is mainly T3.
3,3',5-triiodo-L-thyronine : An iodothyronine compound having iodo substituents at the 3-, 3'- and 5-positions. Although some is produced in the thyroid, most of the 3,3',5-triiodo-L-thyronine in the body is generated by mono-deiodination of L-thyroxine in the peripheral tissues. Its metabolic activity is about 3 to 5 times that of L-thyroxine. The sodium salt is used in the treatment of hypothyroidism.

Hyperthyroxinemia: Abnormally elevated THYROXINE level in the BLOOD.

Research Excerpts

ExcerptRelevanceReference
"Familial dysalbuminemic hyperthyroxinemia (FDH), is the most common cause of inherited increase in serum total T4 (TT4) in the Caucasian population."8.80Familial dysalbuminemic hyperthyroxinemia in a Swiss family caused by a mutant albumin (R218P) shows an apparent discrepancy between serum concentration and affinity for thyroxine. ( Eiholzer, U; Feldman, M; Pannain, S; Refetoff, S; Scherberg, NH; Weiss, RE, 2000)
"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 ligand (analogue or derivative tracer) or labelled antibody (solid-phase antigen-linked technique: SPALT) method."8.79Familial dysalbuminemic hyperthyroxinemia and thyroid hormone autoantibodies: interference in current free thyroid hormone assays. ( Gasser, F; Sapin, R; Schlienger, JL, 1996)
"We demonstrated positive associations of thyroid hormones with prevalent and incident type 2 diabetes mellitus suggesting that hyperthyroxinemia may contribute to the pathogenesis of this condition."7.88Hyperthyroxinemia is positively associated with prevalent and incident type 2 diabetes mellitus in two population-based samples from Northeast Germany and Denmark. ( Dörr, M; Ittermann, T; Jørgensen, T; Markus, MRP; Schipf, S; Thuesen, BH; Völzke, H, 2018)
"The neonates from mothers with AITD, independently of the presence also of TRab in the mothers, had a transient hyperthyroxinemia one week following birth."7.73Transient hyperthyroxinemia in newborns from women with autoimmune thyroid disease and raised levels of thyroid peroxidase antibodies. ( Kvetny, J; Poulsen, H, 2006)
"Familial dysalbuminemic hyperthyroxinemia (FDH) is the most common cause of inherited euthyroid hyperthyroxinemia in Caucasians."7.69A novel missense mutation in codon 218 of the albumin gene in a distinct phenotype of familial dysalbuminemic hyperthyroxinemia in a Japanese kindred. ( Chiba, H; Kijima, H; Koike, T; Kubo, M; Shimizu, C; Wada, N, 1997)
" Missense mutations of the TTR gene produce familial amyloidotic polyneuropathy and rarely, euthyroid hyperthyroxinemia (EHT)."7.69A new family with hyperthyroxinemia caused by transthyretin Val109 misdiagnosed as thyrotoxicosis and resistance to thyroid hormone--a clinical research center study. ( Byrne, MM; Marinov, VS; Refetoff, S; Sunthornthepvarakul, T; Tunca, H; Weiss, RE, 1996)
"To investigate unusual free thyroxine (FT4) responses to T4 replacement doses in a hypothyroid patient with familial dysalbuminemic hyperthyroxinemia (FDH)."7.69Inhibition of serum protein binding of thyroxine in a hypothyroid patient with familial dysalbuminemic hyperthyroxinemia. ( Premachandra, BN; Williams, IK; Wortsman, J, 1996)
"A recent report documented the existence of three putative types of variant albumin in dysalbuminemic hyperthyroxinemia (DH) and suggested that measurement of the total concentration of three iodothyronines (T4, T3 and rT3) in serum of affected subjects could aid in their differentiation."7.68Can the type of variant albumin in familial dysalbuminemic hyperthyroxinemia be determined by measuring iodothyronines in serum? ( Ikegami, Y; Kitaoka, H; Ohsawa, N; Sakane, S; Takamatsu, J; Takeda, K, 1990)
"The effects of pH and anionic binding inhibitors were used to test the hypothesis that the increased T4 binding affinity of the variant albumin (Alb-FDH) of familial dysalbuminemic hyperthyroxinemia (FDH) is due to an electrostatic bond with the ionized phenolic hydroxyl of the iodothyronine."7.68Studies on the nature of iodothyronine binding in familial dysalbuminemic hyperthyroxinemia. ( Divino, CM; Schussler, GC, 1990)
"Serum samples from 21,342 patients undergoing evaluation of thyroid status were screened for familial dysalbuminemic hyperthyroxinemia (FDH) using a specific test based on the measure of charcoal uptake of 125I thyroxine (T4) from serum diluted 1:100 with addition of unlabelled 10(-6) M T4."7.67[Familial hyperthyroxinemia with dysalbuminemia: screening of 21,000 patients at the occasion of thyroid evaluation]. ( Chambron, J; Gasser, F; Sapin, R, 1989)
"Eleven patients, with a history of hypothyroidism, who had hyperthyroxinemia and an elevated free thyroxine index but normal serum triiodothyronine concentrations on levothyroxine replacement underwent levothyroxine dose reduction at three-month intervals until the free thyroxine index fell into the normal range."7.67Hyperthyroxinemia in patients receiving thyroid replacement therapy. ( Grund, FM; Niewoehner, CB, 1989)
"To investigate the role of thyroxine-binding globulin (TBG) and albumin in the availability of thyroid hormones to peripheral tissues, comprehensive kinetic studies of thyroxine (T4) and triiodothyronine (T3) were carried out in eight subjects with familial dysalbuminemic hyperthyroxinemia (FDH), in four subjects with inherited TBG excess, and in 15 normals."7.67Role of serum carrier proteins in the peripheral metabolism and tissue distribution of thyroid hormones in familial dysalbuminemic hyperthyroxinemia and congenital elevation of thyroxine-binding globulin. ( Bianchi, R; Cazzuola, F; Ferdeghini, M; Giraudi, G; Iervasi, G; Pilo, A; Vitek, F, 1987)
" In dysalbuminemic hyperthyroxinemia, about 30% of the serum thyroxin is bound to albumin; in prealbumin-associated hyperthyroxinemia, 7% is bound to prealbumin."7.67Detection of protein binding abnormalities in euthyroid hyperthyroxinemia. ( George, PM; Palmer, BN; Sheat, JM, 1988)
"Examining the course of cardiac arrhythmias (CA) in developed TT has established that this condition gives rise to their recurrence."5.32[The specific features of thyrotoxicosis and euthyroid hyperthyroxinemia developed due to the use of cordarone]. ( Bakalov, SA; Domogadskiĭ, SP; Golitsyn, SP; Kolesnikova, GS; Masenko, VP; Molashenko, NV; Platonova, NM; Serdiuk, SE; Sviridenko, NIu, 2004)
" The effect of hyperthyroxinemia on TAFI was studied in healthy volunteers who were randomised to receive levothyroxine or no medication for 14 days in a crossover design."5.17Thrombin-activatable fibrinolysis inhibitor in hypothyroidism and hyperthyroxinaemia. ( Brandjes, DP; Büller, HR; Gerdes, VE; Meijers, JC; Squizzato, A; Stuijver, DJ; van Zaane, B; Verkleij, CJ, 2013)
"Familial dysalbuminemic hyperthyroxinemia (FDH), is the most common cause of inherited increase in serum total T4 (TT4) in the Caucasian population."4.80Familial dysalbuminemic hyperthyroxinemia in a Swiss family caused by a mutant albumin (R218P) shows an apparent discrepancy between serum concentration and affinity for thyroxine. ( Eiholzer, U; Feldman, M; Pannain, S; Refetoff, S; Scherberg, NH; Weiss, RE, 2000)
"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 ligand (analogue or derivative tracer) or labelled antibody (solid-phase antigen-linked technique: SPALT) method."4.79Familial dysalbuminemic hyperthyroxinemia and thyroid hormone autoantibodies: interference in current free thyroid hormone assays. ( Gasser, F; Sapin, R; Schlienger, JL, 1996)
"We demonstrated positive associations of thyroid hormones with prevalent and incident type 2 diabetes mellitus suggesting that hyperthyroxinemia may contribute to the pathogenesis of this condition."3.88Hyperthyroxinemia is positively associated with prevalent and incident type 2 diabetes mellitus in two population-based samples from Northeast Germany and Denmark. ( Dörr, M; Ittermann, T; Jørgensen, T; Markus, MRP; Schipf, S; Thuesen, BH; Völzke, H, 2018)
" Normal values of thyrotropin (TSH) and increased values of THs are referred to as hyperthyroxinemia, while normal values of thyrotropin and decreased values of thyroid hormone are hypothyroxinemia."3.79Dysthyronemia in normal concentrations of thyrotropin--analytical and clinical consequences. ( Bílek, R; Stárka, L; Zamrazil, V, 2013)
"The neonates from mothers with AITD, independently of the presence also of TRab in the mothers, had a transient hyperthyroxinemia one week following birth."3.73Transient hyperthyroxinemia in newborns from women with autoimmune thyroid disease and raised levels of thyroid peroxidase antibodies. ( Kvetny, J; Poulsen, H, 2006)
"All 7 patients had hyperthyroidism, elevated free thyroxine or triiodothyronine levels, and unsuppressed levels of TSH."3.72Clinical characteristics of patients with thyrotropin-secreting pituitary adenoma. ( Chang, HY; Chen, KW; Huang, YY; Jung, SM; Lin, JD; Wu, YY, 2003)
"Over a 20-month period, 101 infants (51 boys) and their mothers enrolled in the study (of 241 eligible infants), from a total screening population of 80,884; 17 infants were identified with persistent hyperthyroxinemia (TT4 >16 microg/dL)."3.72Follow-up of newborns with elevated screening T4 concentrations. ( Brent, GA; Lafranchi, SH; Nelson, JC; Sesser, DE; Singh, N; Skeels, MR; Snyder, DB, 2003)
"Euthyroid hyperthyroxinemia as a result of a transient increase in thyroid-stimulating hormone (TSH) levels may contribute to the development of manic disorder."3.70Thyroid function and psychiatric morbidity in patients with manic disorder receiving lithium therapy. ( Ahuja, A; Chow, CC; Lee, DT; Lee, S; Leung, TY; Mak, TW; Shek, AC; Wing, YK, 2000)
"Familial dysalbuminemic hyperthyroxinemia (FDH) is the most common cause of inherited euthyroid hyperthyroxinemia in Caucasians."3.69A novel missense mutation in codon 218 of the albumin gene in a distinct phenotype of familial dysalbuminemic hyperthyroxinemia in a Japanese kindred. ( Chiba, H; Kijima, H; Koike, T; Kubo, M; Shimizu, C; Wada, N, 1997)
" Missense mutations of the TTR gene produce familial amyloidotic polyneuropathy and rarely, euthyroid hyperthyroxinemia (EHT)."3.69A new family with hyperthyroxinemia caused by transthyretin Val109 misdiagnosed as thyrotoxicosis and resistance to thyroid hormone--a clinical research center study. ( Byrne, MM; Marinov, VS; Refetoff, S; Sunthornthepvarakul, T; Tunca, H; Weiss, RE, 1996)
"To investigate unusual free thyroxine (FT4) responses to T4 replacement doses in a hypothyroid patient with familial dysalbuminemic hyperthyroxinemia (FDH)."3.69Inhibition of serum protein binding of thyroxine in a hypothyroid patient with familial dysalbuminemic hyperthyroxinemia. ( Premachandra, BN; Williams, IK; Wortsman, J, 1996)
"Recently, a transthyretin variant, TTR Met 119, in which methionine substitutes for threonine 119, a component of the protein's iodothyronine binding site, was identified in individuals with transient euthyroid hyperthyroxinemia."3.68Thyroxine binding in a TTR Met 119 kindred. ( Almeida, MR; Altland, K; Alves, IL; Coelho, T; Costa, PP; Divino, CM; Palha, JA; Saraiva, MJ; Schussler, GC, 1993)
"A recent report documented the existence of three putative types of variant albumin in dysalbuminemic hyperthyroxinemia (DH) and suggested that measurement of the total concentration of three iodothyronines (T4, T3 and rT3) in serum of affected subjects could aid in their differentiation."3.68Can the type of variant albumin in familial dysalbuminemic hyperthyroxinemia be determined by measuring iodothyronines in serum? ( Ikegami, Y; Kitaoka, H; Ohsawa, N; Sakane, S; Takamatsu, J; Takeda, K, 1990)
"The effects of pH and anionic binding inhibitors were used to test the hypothesis that the increased T4 binding affinity of the variant albumin (Alb-FDH) of familial dysalbuminemic hyperthyroxinemia (FDH) is due to an electrostatic bond with the ionized phenolic hydroxyl of the iodothyronine."3.68Studies on the nature of iodothyronine binding in familial dysalbuminemic hyperthyroxinemia. ( Divino, CM; Schussler, GC, 1990)
" 16 cases with increased T4, FT4 were diagnosed as euthyroid hyperthyroxinemia."3.68[Changes in serum thyroid hormones in acute cerebrovascular apoplexy and their clinical significance]. ( Hu, R, 1990)
" In dysalbuminemic hyperthyroxinemia, about 30% of the serum thyroxin is bound to albumin; in prealbumin-associated hyperthyroxinemia, 7% is bound to prealbumin."3.67Detection of protein binding abnormalities in euthyroid hyperthyroxinemia. ( George, PM; Palmer, BN; Sheat, JM, 1988)
"The diagnosis of partial peripheral and pituitary resistance to thyroid hormone was ultimately made in two boys, 7 and 9 years of age, and a 10-year-old girl who had goiters and hyperthyroxinemia."3.67Familial partial peripheral and pituitary resistance to thyroid hormone: a frequently missed diagnosis? ( Hopwood, NJ; Saunder, SE; Shapiro, B; Sisson, JC, 1986)
"Serum samples from 21,342 patients undergoing evaluation of thyroid status were screened for familial dysalbuminemic hyperthyroxinemia (FDH) using a specific test based on the measure of charcoal uptake of 125I thyroxine (T4) from serum diluted 1:100 with addition of unlabelled 10(-6) M T4."3.67[Familial hyperthyroxinemia with dysalbuminemia: screening of 21,000 patients at the occasion of thyroid evaluation]. ( Chambron, J; Gasser, F; Sapin, R, 1989)
"To investigate the role of thyroxine-binding globulin (TBG) and albumin in the availability of thyroid hormones to peripheral tissues, comprehensive kinetic studies of thyroxine (T4) and triiodothyronine (T3) were carried out in eight subjects with familial dysalbuminemic hyperthyroxinemia (FDH), in four subjects with inherited TBG excess, and in 15 normals."3.67Role of serum carrier proteins in the peripheral metabolism and tissue distribution of thyroid hormones in familial dysalbuminemic hyperthyroxinemia and congenital elevation of thyroxine-binding globulin. ( Bianchi, R; Cazzuola, F; Ferdeghini, M; Giraudi, G; Iervasi, G; Pilo, A; Vitek, F, 1987)
"Eleven patients, with a history of hypothyroidism, who had hyperthyroxinemia and an elevated free thyroxine index but normal serum triiodothyronine concentrations on levothyroxine replacement underwent levothyroxine dose reduction at three-month intervals until the free thyroxine index fell into the normal range."3.67Hyperthyroxinemia in patients receiving thyroid replacement therapy. ( Grund, FM; Niewoehner, CB, 1989)
"Hyperthyroidism was associated with an increased risk of preterm birth (PTB, adjusted OR: 2."1.62Impact of maternal thyroid hormone in late pregnancy on adverse birth outcomes: A retrospective cohort study in China. ( Gao, Y; Wang, H; Wang, J; Yu, B; Yuan, X, 2021)
"Examining the course of cardiac arrhythmias (CA) in developed TT has established that this condition gives rise to their recurrence."1.32[The specific features of thyrotoxicosis and euthyroid hyperthyroxinemia developed due to the use of cordarone]. ( Bakalov, SA; Domogadskiĭ, SP; Golitsyn, SP; Kolesnikova, GS; Masenko, VP; Molashenko, NV; Platonova, NM; Serdiuk, SE; Sviridenko, NIu, 2004)

Research

Studies (45)

TimeframeStudies, this research(%)All Research%
pre-199013 (28.89)18.7374
1990's17 (37.78)18.2507
2000's8 (17.78)29.6817
2010's6 (13.33)24.3611
2020's1 (2.22)2.80

Authors

AuthorsStudies
Yuan, X1
Wang, J1
Gao, Y1
Wang, H1
Yu, B1
Ittermann, T1
Schipf, S1
Dörr, M1
Thuesen, BH1
Jørgensen, T1
Völzke, H1
Markus, MRP1
Bílek, R1
Stárka, L1
Zamrazil, V1
Sala, A1
Labrador-Horrillo, M1
Guilarte, M1
Luengo, O1
Rueda, M1
Cardona, V1
Akcay, T1
Turan, S1
Guran, T1
Unluguzel, G1
Haklar, G1
Bereket, A1
Gurnell, M1
Halsall, DJ1
Chatterjee, VK1
Monfoulet, LE1
Rabier, B1
Dacquin, R1
Anginot, A1
Photsavang, J1
Jurdic, P1
Vico, L1
Malaval, L1
Chassande, O1
Verkleij, CJ1
Stuijver, DJ1
van Zaane, B1
Squizzato, A1
Brandjes, DP1
Büller, HR1
Meijers, JC1
Gerdes, VE1
Wu, YY1
Chang, HY1
Lin, JD1
Chen, KW1
Huang, YY1
Jung, SM1
Lafranchi, SH1
Snyder, DB1
Sesser, DE1
Skeels, MR1
Singh, N1
Brent, GA1
Nelson, JC1
Molashenko, NV1
Sviridenko, NIu1
Platonova, NM1
Kolesnikova, GS1
Golitsyn, SP1
Bakalov, SA1
Serdiuk, SE1
Masenko, VP1
Domogadskiĭ, SP1
Kvetny, J2
Poulsen, H1
Langsteger, W1
Stockigt, JR1
Docter, R1
Költringer, P1
Lorenz, O1
Eber, O1
Bergenfelz, A1
Ahrén, B1
Alves, IL1
Divino, CM2
Schussler, GC2
Altland, K1
Almeida, MR1
Palha, JA1
Coelho, T1
Costa, PP1
Saraiva, MJ1
Tokmakjian, S1
Haines, M1
Edmonds, M1
Refetoff, S2
Marinov, VS1
Tunca, H1
Byrne, MM1
Sunthornthepvarakul, T1
Weiss, RE2
Premachandra, BN1
Wortsman, J1
Williams, IK1
Sapin, R2
Gasser, F2
Schlienger, JL1
Ghayad, E1
Choueiri Medlej, R1
Wada, N1
Chiba, H1
Shimizu, C1
Kijima, H1
Kubo, M1
Koike, T1
López, JM1
Mosso, L1
Campino, C1
Lee, S1
Chow, CC1
Wing, YK1
Shek, AC1
Mak, TW1
Ahuja, A1
Lee, DT1
Leung, TY1
Pannain, S1
Feldman, M1
Eiholzer, U1
Scherberg, NH1
Laji, K1
Rhidha, B1
John, R1
Lazarus, J1
Davies, JS1
Flechner, I1
Aranoff, G1
Reifen, R1
Landau, H1
Crothers, DC1
Harvey, TC1
Faber, J1
Ramsden, DB1
O'Hare, J1
Abuaisha, B1
Barrett, E1
Takamatsu, J1
Ikegami, Y1
Sakane, S1
Kitaoka, H1
Takeda, K1
Ohsawa, N1
Hu, R1
Matzen, LE1
Brøns, M1
Tucker, WS1
Ober, KP1
Lowder, SC1
Chambron, J1
Grund, FM1
Niewoehner, CB1
Mulligan, GP1
Davidson, JS1
Kaplan, H1
Abrahamson, MJ1
Avalos, E1
De Nayer, P1
Beckers, C1
Hopwood, NJ1
Saunder, SE1
Shapiro, B1
Sisson, JC1
Lalloz, MR1
Byfield, PG1
Goel, KM1
Loudon, MM1
Thomson, JA1
Himsworth, RL1
Bianchi, R1
Iervasi, G1
Pilo, A1
Vitek, F1
Ferdeghini, M1
Cazzuola, F1
Giraudi, G1
Nakamura, H1
George, PM1
Sheat, JM1
Palmer, BN1
Fleming, SJ1
Applegate, GF1
Beardwell, CG1

Reviews

4 reviews available for triiodothyronine and Hyperthyroxinemia

ArticleYear
Familial dysalbuminemic hyperthyroxinemia and thyroid hormone autoantibodies: interference in current free thyroid hormone assays.
    Hormone research, 1996, Volume: 45, Issue:3-5

    Topics: Autoantibodies; Humans; Hyperthyroxinemia; Methods; Serum Albumin; Thyroid Hormones; Thyroxine; Trii

1996
[Changes in thyroid tests in non-thyroid diseases].
    Le Journal medical libanais. The Lebanese medical journal, 1996, Volume: 44, Issue:1

    Topics: Disease; Drug-Related Side Effects and Adverse Reactions; Humans; Hyperthyroxinemia; Thyroid Hormone

1996
Familial dysalbuminemic hyperthyroxinemia in a Swiss family caused by a mutant albumin (R218P) shows an apparent discrepancy between serum concentration and affinity for thyroxine.
    The Journal of clinical endocrinology and metabolism, 2000, Volume: 85, Issue:8

    Topics: Amino Acid Substitution; Child, Preschool; DNA; Female; Genotype; Humans; Hyperthyroxinemia; Male; P

2000
Abnormal serum free thyroid hormone levels due to heparin administration.
    QJM : monthly journal of the Association of Physicians, 2001, Volume: 94, Issue:9

    Topics: Adult; Anticoagulants; Female; Heparin; Humans; Hyperthyroxinemia; Male; Middle Aged; Thyrotropin; T

2001

Trials

2 trials available for triiodothyronine and Hyperthyroxinemia

ArticleYear
T4 plus T3 treatment in children with hypothyroidism and inappropriately elevated thyroid-stimulating hormone despite euthyroidism on T4 treatment.
    Hormone research in paediatrics, 2010, Volume: 73, Issue:2

    Topics: Child; Child, Preschool; Congenital Hypothyroidism; Female; Humans; Hyperthyroxinemia; Male; Pituita

2010
Thrombin-activatable fibrinolysis inhibitor in hypothyroidism and hyperthyroxinaemia.
    Thrombosis and haemostasis, 2013, Volume: 109, Issue:2

    Topics: Adult; Aged; Aged, 80 and over; Blood Coagulation; Carboxypeptidase B2; Cross-Over Studies; Female;

2013

Other Studies

39 other studies available for triiodothyronine and Hyperthyroxinemia

ArticleYear
Impact of maternal thyroid hormone in late pregnancy on adverse birth outcomes: A retrospective cohort study in China.
    Endocrine journal, 2021, Mar-28, Volume: 68, Issue:3

    Topics: Adult; China; Cohort Studies; Female; Fetal Macrosomia; Humans; Hyperthyroidism; Hyperthyroxinemia;

2021
Hyperthyroxinemia is positively associated with prevalent and incident type 2 diabetes mellitus in two population-based samples from Northeast Germany and Denmark.
    Nutrition, metabolism, and cardiovascular diseases : NMCD, 2018, Volume: 28, Issue:2

    Topics: Adult; Aged; Biomarkers; Cross-Sectional Studies; Denmark; Diabetes Mellitus, Type 2; Female; German

2018
Dysthyronemia in normal concentrations of thyrotropin--analytical and clinical consequences.
    Hormone molecular biology and clinical investigation, 2013, Volume: 13, Issue:2

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Female; Humans; Hyperthyroxinemia; Male; Middle Aged; Re

2013
Immediate-type hypersensitivity reaction to levothyroxine and desensitization.
    Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology, 2008, Volume: 100, Issue:5

    Topics: Aged; Desensitization, Immunologic; Female; Humans; Hypersensitivity, Immediate; Hyperthyroxinemia;

2008
What should be done when thyroid function tests do not make sense?
    Clinical endocrinology, 2011, Volume: 74, Issue:6

    Topics: Algorithms; Diagnosis, Differential; Humans; Hyperthyroxinemia; Reproducibility of Results; Sensitiv

2011
Thyroid hormone receptor β mediates thyroid hormone effects on bone remodeling and bone mass.
    Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2011, Volume: 26, Issue:9

    Topics: Aging; Animals; Bone and Bones; Bone Density; Bone Remodeling; Bone Resorption; Hyperthyroxinemia; M

2011
Clinical characteristics of patients with thyrotropin-secreting pituitary adenoma.
    Journal of the Formosan Medical Association = Taiwan yi zhi, 2003, Volume: 102, Issue:3

    Topics: Acromegaly; Adenoma; Adult; Aged; Female; Human Growth Hormone; Humans; Hyperthyroidism; Hyperthyrox

2003
Follow-up of newborns with elevated screening T4 concentrations.
    The Journal of pediatrics, 2003, Volume: 143, Issue:3

    Topics: Female; Follow-Up Studies; Humans; Hyperthyroxinemia; Incidence; Infant; Infant, Newborn; Male; Neon

2003
[The specific features of thyrotoxicosis and euthyroid hyperthyroxinemia developed due to the use of cordarone].
    Klinicheskaia meditsina, 2004, Volume: 82, Issue:12

    Topics: Amiodarone; Anti-Arrhythmia Agents; Arrhythmias, Cardiac; Autoantibodies; Blood Flow Velocity; Elect

2004
Transient hyperthyroxinemia in newborns from women with autoimmune thyroid disease and raised levels of thyroid peroxidase antibodies.
    The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians, 2006, Volume: 19, Issue:12

    Topics: Autoantibodies; Bilirubin; Blood Glucose; Female; Fetal Blood; Humans; Hyperthyroxinemia; Infant, Ne

2006
Familial dysalbuminaemic hyperthyroxinaemia and inherited partial TBG deficiency: first report.
    Clinical endocrinology, 1994, Volume: 40, Issue:6

    Topics: Adult; Aged; Electrophoresis, Agar Gel; Humans; Hyperthyroxinemia; Male; Pedigree; Prealbumin; Prote

1994
Hyperthyroxinemia after surgery for primary hyperparathyroidism.
    Langenbecks Archiv fur Chirurgie, 1994, Volume: 379, Issue:3

    Topics: Adult; Aged; Calcium; Cholecystectomy, Laparoscopic; Female; Humans; Hyperparathyroidism; Hyperthyro

1994
Thyroxine binding in a TTR Met 119 kindred.
    The Journal of clinical endocrinology and metabolism, 1993, Volume: 77, Issue:2

    Topics: Amyloidosis; Asparagine; Binding Sites; DNA; Female; Genotype; Heterozygote; Humans; Hyperthyroxinem

1993
Free thyroxine measured by the Ciba Corning ACS-180 on samples from patients with familial dysalbuminemic hyperthyroxinemia.
    Clinical chemistry, 1993, Volume: 39, Issue:8

    Topics: Autoanalysis; Humans; Hyperthyroxinemia; Serum Albumin; Thyroxine; Triiodothyronine

1993
A new family with hyperthyroxinemia caused by transthyretin Val109 misdiagnosed as thyrotoxicosis and resistance to thyroid hormone--a clinical research center study.
    The Journal of clinical endocrinology and metabolism, 1996, Volume: 81, Issue:9

    Topics: Adolescent; Adult; Aged; Base Sequence; Diagnosis, Differential; Female; Humans; Hyperthyroxinemia;

1996
Inhibition of serum protein binding of thyroxine in a hypothyroid patient with familial dysalbuminemic hyperthyroxinemia.
    Clinical biochemistry, 1996, Volume: 29, Issue:1

    Topics: Aged; Female; Humans; Hyperthyroxinemia; Hypothyroidism; Protein Binding; Serum Albumin; Thyroid Fun

1996
A novel missense mutation in codon 218 of the albumin gene in a distinct phenotype of familial dysalbuminemic hyperthyroxinemia in a Japanese kindred.
    The Journal of clinical endocrinology and metabolism, 1997, Volume: 82, Issue:10

    Topics: Adult; Amino Acid Sequence; Asian People; Carrier Proteins; Codon; Female; Genome; Humans; Hyperthyr

1997
[Hyperthyroxinemia and clinical euthyroidism. Report of one case].
    Revista medica de Chile, 1999, Volume: 127, Issue:2

    Topics: Adult; Euthyroid Sick Syndromes; Humans; Hyperthyroxinemia; Male; Serum Albumin; Thyrotropin; Thyrox

1999
Thyroid function and psychiatric morbidity in patients with manic disorder receiving lithium therapy.
    Journal of clinical psychopharmacology, 2000, Volume: 20, Issue:2

    Topics: Adult; Antimanic Agents; Bipolar Disorder; Euthyroid Sick Syndromes; Female; Follow-Up Studies; Huma

2000
Detection of albumin binding abnormalities in sera of patients with familial dysalbuminaemic hyperthyroxinaemia using isoelectric focusing.
    Endocrine research, 1992, Volume: 18, Issue:3

    Topics: Adult; Albumins; Electrophoresis, Agar Gel; Female; Humans; Hyperthyroxinemia; Infant; Infant, Newbo

1992
Familial non-toxic hyperthyroxinaemia: receptor or 5'-deiodinase defect or deficiency.
    Annals of clinical biochemistry, 1992, Volume: 29 ( Pt 1)

    Topics: Adult; Family Health; Female; Goiter; Humans; Hyperthyroxinemia; Hypothyroidism; Iodide Peroxidase;

1992
Audit of hyperthyroxinaemia and thyrotoxicosis using a sensitive TSH assay.
    Irish medical journal, 1991, Volume: 84, Issue:2

    Topics: Humans; Hyperthyroxinemia; Retrospective Studies; Thyrotoxicosis; Thyrotropin; Thyroxine; Thyroxine-

1991
Can the type of variant albumin in familial dysalbuminemic hyperthyroxinemia be determined by measuring iodothyronines in serum?
    Endocrinologia japonica, 1990, Volume: 37, Issue:3

    Topics: Adult; Female; Humans; Hyperthyroxinemia; Pedigree; Serum Albumin; Thyroxine; Triiodothyronine; Trii

1990
Studies on the nature of iodothyronine binding in familial dysalbuminemic hyperthyroxinemia.
    The Journal of clinical endocrinology and metabolism, 1990, Volume: 71, Issue:1

    Topics: Aspirin; Binding Sites; Chlorides; Female; Hot Temperature; Humans; Hydrogen-Ion Concentration; Hype

1990
[Changes in serum thyroid hormones in acute cerebrovascular apoplexy and their clinical significance].
    Zhonghua shen jing jing shen ke za zhi = Chinese journal of neurology and psychiatry, 1990, Volume: 23, Issue:2

    Topics: Adult; Aged; Aged, 80 and over; Cerebrovascular Disorders; Female; Humans; Hyperthyroxinemia; Male;

1990
Evidence of both decreased nuclear receptor-binding of T3 and inhibited thyroid hormone-stimulated glucose-uptake in cells from a euthyroid patient with hyperthyroxinaemia.
    Scandinavian journal of clinical and laboratory investigation, 1990, Volume: 50, Issue:4

    Topics: Blood Glucose; Cell Nucleus; Humans; Hyperthyroxinemia; Leukocytes, Mononuclear; Male; Middle Aged;

1990
Euthyroid hyperthyroxinemia due to familial excess of thyroxine-binding globulin.
    Southern medical journal, 1989, Volume: 82, Issue:3

    Topics: Adult; Diagnosis, Differential; Euthyroid Sick Syndromes; Humans; Hyperthyroxinemia; Male; Pedigree;

1989
Massive hyperthyroxinemia in a euthyroid patient with hepatocellular carcinoma.
    The American journal of medicine, 1989, Volume: 86, Issue:5

    Topics: Aged; Carcinoma, Hepatocellular; Female; Humans; Hyperthyroxinemia; Liver Neoplasms; Triiodothyronin

1989
[Familial hyperthyroxinemia with dysalbuminemia: screening of 21,000 patients at the occasion of thyroid evaluation].
    Pathologie-biologie, 1989, Volume: 37, Issue:7

    Topics: Humans; Hyperthyroxinemia; Mass Screening; Serum Albumin; Thyroid Function Tests; Thyrotropin; Thyro

1989
Hyperthyroxinemia in patients receiving thyroid replacement therapy.
    Archives of internal medicine, 1989, Volume: 149, Issue:4

    Topics: Adult; Aged; Body Weight; Creatinine; Female; Hemodynamics; Humans; Hyperthyroxinemia; Hypothyroidis

1989
Euthyroid hyperthyroxinaemia.
    Lancet (London, England), 1987, Jul-18, Volume: 2, Issue:8551

    Topics: Adolescent; Female; Humans; Hyperthyroxinemia; Male; Thyroid Gland; Thyroxine-Binding Proteins; Trii

1987
Euthyroid hyperthyroxinaemia due to endogenous antibodies to thyroxine and tri-iodothyronine. A case report.
    South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde, 1989, Feb-18, Volume: 75, Issue:4

    Topics: Autoantibodies; Diagnosis, Differential; Female; Humans; Hyperthyroxinemia; Middle Aged; Thyrotoxico

1989
Diagnostic value of free triiodothyronine in serum.
    Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 1986, Volume: 27, Issue:11

    Topics: Evaluation Studies as Topic; Female; Humans; Hyperthyroidism; Hyperthyroxinemia; Hypothyroidism; Mal

1986
Familial partial peripheral and pituitary resistance to thyroid hormone: a frequently missed diagnosis?
    Pediatrics, 1986, Volume: 78, Issue:6

    Topics: Child; Female; Goiter; Humans; Hyperthyroxinemia; Male; Pedigree; Pituitary Gland; Prolactin; Thyroi

1986
Hyperthyroxinemia due to the coexistence of two raised affinity thyroxine-binding proteins (albumin and prealbumin) in one family.
    The Journal of clinical endocrinology and metabolism, 1987, Volume: 64, Issue:2

    Topics: Adolescent; Adult; Aged; Blood Protein Electrophoresis; Child; Female; Humans; Hyperthyroxinemia; Ma

1987
Role of serum carrier proteins in the peripheral metabolism and tissue distribution of thyroid hormones in familial dysalbuminemic hyperthyroxinemia and congenital elevation of thyroxine-binding globulin.
    The Journal of clinical investigation, 1987, Volume: 80, Issue:2

    Topics: Adult; Aged; Humans; Hyperthyroxinemia; Metabolic Clearance Rate; Middle Aged; Serum Albumin; Thyroi

1987
[Syndromes of thyroid hormone resistance--Refetoff syndromes].
    Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme, 1988, Volume: 33, Issue:5

    Topics: Humans; Hyperthyroxinemia; Syndrome; Thyrotropin; Triiodothyronine

1988
Detection of protein binding abnormalities in euthyroid hyperthyroxinemia.
    Clinical chemistry, 1988, Volume: 34, Issue:9

    Topics: Autoantibodies; Blood Proteins; Humans; Hyperthyroxinemia; Prealbumin; Protein Binding; Serum Albumi

1988
Familial dysalbuminaemic hyperthyroxinaemia.
    Postgraduate medical journal, 1987, Volume: 63, Issue:738

    Topics: Adult; Child; Humans; Hyperthyroxinemia; Male; Middle Aged; Serum Albumin; Thyrotropin; Triiodothyro

1987