triiodothyronine has been researched along with Developmental Psychomotor Disorders in 9 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 |
|---|---|---|
| "To identify the molecular defect by which psychomotor retardation is caused in two brothers with congenital hypothyroidism who received adequate treatment with l-thyroxine." | 3.72 | A new heterozygous mutation (L338N) in the human Gsalpha (GNAS1) gene as a cause for congenital hypothyroidism in Albright's hereditary osteodystrophy. ( Ahrens, W; Hiort, O; Pohlenz, J, 2003) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (11.11) | 18.7374 |
| 1990's | 1 (11.11) | 18.2507 |
| 2000's | 5 (55.56) | 29.6817 |
| 2010's | 2 (22.22) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Vlaeminck-Guillem, V | 1 |
| Espiard, S | 1 |
| Flamant, F | 1 |
| Wémeau, JL | 2 |
| Kersseboom, S | 1 |
| Visser, TJ | 4 |
| Pohlenz, J | 1 |
| Ahrens, W | 1 |
| Hiort, O | 1 |
| Friesema, EC | 2 |
| Jansen, J | 2 |
| Heuer, H | 1 |
| Trajkovic, M | 1 |
| Bauer, K | 1 |
| Kester, MH | 1 |
| Milici, C | 1 |
| Reeser, M | 1 |
| Grüters, A | 1 |
| Barrett, TG | 1 |
| Mancilla, EE | 1 |
| Svensson, J | 1 |
| Busi da Silva Canalli, MH | 1 |
| Lundgren, J | 1 |
| McEntagart, ME | 1 |
| Hopper, N | 1 |
| Arts, WF | 1 |
| Spiliotis, BE | 1 |
| Samson, JA | 1 |
| Mirin, SM | 1 |
| Griffin, M | 1 |
| Borrelli, D | 1 |
| Schildkraut, JJ | 1 |
| Lehr, HJ | 1 |
| Werner, H | 1 |
| Rudorff, KH | 1 |
| Herrmann, J | 1 |
3 reviews available for triiodothyronine and Developmental Psychomotor Disorders
| Article | Year |
|---|---|
TRα receptor mutations extend the spectrum of syndromes of reduced sensitivity to thyroid hormone.
Topics: Abnormalities, Multiple; Adolescent; Adult; Age of Onset; Bradycardia; Child; Codon, Nonsense; Dwarf | 2015 |
Mechanisms of disease: psychomotor retardation and high T3 levels caused by mutations in monocarboxylate transporter 8.
Topics: Amino Acid Sequence; Animals; Carrier Proteins; Genetic Testing; Humans; Kidney; Liver; Male; Mice; | 2006 |
Thyroid hormone transporters.
Topics: Brain; Carrier Proteins; Cell Membrane; Chromosomes, Human, X; Drug Resistance; Humans; Male; Monoca | 2007 |
6 other studies available for triiodothyronine and Developmental Psychomotor Disorders
| Article | Year |
|---|---|
MCT8: from gene to disease and therapeutic approach.
Topics: Amino Acid Sequence; Amino Acid Transport Systems, Neutral; Animals; Brain; Humans; Kidney; Male; Mi | 2011 |
A new heterozygous mutation (L338N) in the human Gsalpha (GNAS1) gene as a cause for congenital hypothyroidism in Albright's hereditary osteodystrophy.
Topics: Calcium; Child; Erythrocyte Membrane; Fibrous Dysplasia, Polyostotic; Genotype; GTP-Binding Protein | 2003 |
Functional analysis of monocarboxylate transporter 8 mutations identified in patients with X-linked psychomotor retardation and elevated serum triiodothyronine.
Topics: Cell Line, Tumor; Codon, Nonsense; Gene Deletion; Genetic Diseases, X-Linked; Humans; Intellectual D | 2007 |
Pediatric topic: expanding the spectrum of Noonan syndrome.
Topics: Adult; Humans; Infant; Monocarboxylic Acid Transporters; Mutation; Noonan Syndrome; Protein Tyrosine | 2007 |
Urinary MHPG and clinical symptoms in patients with unipolar depression.
Topics: Adult; Body Weight; Cognition Disorders; Depressive Disorder; Dexamethasone; Female; Humans; Hydroco | 1994 |
[T3-thyrotoxicosis in a 3-year-old girl (author's transl)].
Topics: Age Determination by Skeleton; Bone Development; Child, Preschool; Diarrhea; Exophthalmos; Female; G | 1974 |