triiodothyronine has been researched along with Familial Dysalbuminemic Hyperthyroxinemia in 3 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.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Familial dysalbuminemic hyperthyroxinemia (FDH) is a common cause of euthyroid hyperthyroxinemia." | 7.80 | A novel mutation in the Albumin gene (R218S) causing familial dysalbuminemic hyperthyroxinemia in a family of Bangladeshi extraction. ( Cody, V; Dumitrescu, AM; Ferrara, AM; Greenberg, SM; Nicholas, ES; Refetoff, S; Weiss, RE, 2014) |
| "Familial dysalbuminemic hyperthyroxinemia (FDH) is a common cause of euthyroid hyperthyroxinemia." | 3.80 | A novel mutation in the Albumin gene (R218S) causing familial dysalbuminemic hyperthyroxinemia in a family of Bangladeshi extraction. ( Cody, V; Dumitrescu, AM; Ferrara, AM; Greenberg, SM; Nicholas, ES; Refetoff, S; Weiss, RE, 2014) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 1 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Khoo, S | 1 |
| Lyons, G | 1 |
| McGowan, A | 1 |
| Gurnell, M | 1 |
| Oddy, S | 1 |
| Visser, WE | 1 |
| van den Berg, S | 1 |
| Halsall, D | 1 |
| Taylor, K | 1 |
| Chatterjee, K | 1 |
| Moran, C | 1 |
| Greenberg, SM | 1 |
| Ferrara, AM | 1 |
| Nicholas, ES | 1 |
| Dumitrescu, AM | 1 |
| Cody, V | 1 |
| Weiss, RE | 1 |
| Refetoff, S | 1 |
| Dai, WX | 1 |
| Liu, ZY | 1 |
| Guo, ZS | 1 |
| Liu, ZX | 1 |
| Dou, YL | 1 |
3 other studies available for triiodothyronine and Familial Dysalbuminemic Hyperthyroxinemia
| Article | Year |
|---|---|
Familial dysalbuminaemic hyperthyroxinaemia interferes with current free thyroid hormone immunoassay methods.
Topics: Humans; Hyperthyroxinemia, Familial Dysalbuminemic; Immunoassay; Thyroid Function Tests; Thyroid Hor | 2020 |
A novel mutation in the Albumin gene (R218S) causing familial dysalbuminemic hyperthyroxinemia in a family of Bangladeshi extraction.
Topics: Asian People; Bangladesh; Canada; Female; Humans; Hyperthyroxinemia, Familial Dysalbuminemic; Mutati | 2014 |
[A family with familial dysalbuminaemic hyperthyroxinaemia].
Topics: Adult; Base Sequence; DNA Mutational Analysis; Family Health; Female; Humans; Hyperthyroxinemia, Fam | 2005 |