thyroxine has been researched along with Deafness, Transitory in 8 studies
Thyroxine: The major hormone derived from the thyroid gland. Thyroxine is synthesized via the iodination of tyrosines (MONOIODOTYROSINE) and the coupling of iodotyrosines (DIIODOTYROSINE) in the THYROGLOBULIN. Thyroxine is released from thyroglobulin by proteolysis and secreted into the blood. Thyroxine is peripherally deiodinated to form TRIIODOTHYRONINE which exerts a broad spectrum of stimulatory effects on cell metabolism.
thyroxine : An iodothyronine compound having iodo substituents at the 3-, 3'-, 5- and 5'-positions.
| Excerpt | Relevance | Reference |
|---|---|---|
| " Premature infants often require outpatient care for bronchopulmonary dysplasia, apnea, retinopathy of prematurity, intraventricular hemorrhage, hearing loss, hypothyroxinemia, anemia, neurodevelopmental sequelae, assessment of growth and nutrition, immunizations, and psychosocial stress." | 4.77 | Continuing care for the preterm infant after dismissal from the neonatal intensive care unit. ( Berseth, CL; Swanson, JA, 1987) |
| "The prevalence of hearing impairment was shown to depend on the etiological variant of CPH." | 1.40 | [The hearing function in the patients presenting with congenital primary hypothyroidism]. ( Geptner, EN, 2014) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (37.50) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (37.50) | 29.6817 |
| 2010's | 2 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Geptner, EN | 1 |
| Heinen, CA | 1 |
| Losekoot, M | 1 |
| Sun, Y | 1 |
| Watson, PJ | 1 |
| Fairall, L | 1 |
| Joustra, SD | 1 |
| Zwaveling-Soonawala, N | 1 |
| Oostdijk, W | 1 |
| van den Akker, EL | 1 |
| Alders, M | 1 |
| Santen, GW | 1 |
| van Rijn, RR | 1 |
| Dreschler, WA | 1 |
| Surovtseva, OV | 1 |
| Biermasz, NR | 1 |
| Hennekam, RC | 1 |
| Wit, JM | 1 |
| Schwabe, JW | 1 |
| Boelen, A | 1 |
| Fliers, E | 1 |
| van Trotsenburg, AS | 1 |
| HOLLANDER, CS | 1 |
| PROUT, TE | 1 |
| RIENHOFF, M | 1 |
| RUBEN, RJ | 1 |
| ASPER, SP | 1 |
| Ng, L | 1 |
| Goodyear, RJ | 1 |
| Woods, CA | 1 |
| Schneider, MJ | 1 |
| Diamond, E | 1 |
| Richardson, GP | 1 |
| Kelley, MW | 1 |
| Germain, DL | 1 |
| Galton, VA | 1 |
| Forrest, D | 1 |
| Johnson, KR | 1 |
| Marden, CC | 1 |
| Ward-Bailey, P | 1 |
| Gagnon, LH | 1 |
| Bronson, RT | 1 |
| Donahue, LR | 1 |
| Guipponi, M | 1 |
| Tan, J | 1 |
| Cannon, PZ | 1 |
| Donley, L | 1 |
| Crewther, P | 1 |
| Clarke, M | 1 |
| Wu, Q | 1 |
| Shepherd, RK | 1 |
| Scott, HS | 1 |
| Van't Hoff, W | 1 |
| Stuart, DW | 1 |
| Swanson, JA | 1 |
| Berseth, CL | 1 |
1 review available for thyroxine and Deafness, Transitory
| Article | Year |
|---|---|
Continuing care for the preterm infant after dismissal from the neonatal intensive care unit.
Topics: Anemia, Neonatal; Apnea; Bronchopulmonary Dysplasia; Cerebral Hemorrhage; Hearing Loss; Humans; Infa | 1987 |
7 other studies available for thyroxine and Deafness, Transitory
| Article | Year |
|---|---|
[The hearing function in the patients presenting with congenital primary hypothyroidism].
Topics: Adolescent; Audiometry; Child; Child, Preschool; Congenital Hypothyroidism; Early Diagnosis; Female; | 2014 |
Mutations in TBL1X Are Associated With Central Hypothyroidism.
Topics: Adolescent; Adult; Child; Female; Hearing Loss; Heterozygote; Humans; Hypothalamus; Hypothyroidism; | 2016 |
CONGENITAL DEAFNESS AND GOITER. STUDIES OF A PATIENT WITH A COCHLEAR DEFECT AND INADEQUATE FORMATION OF IODOTHYRONINES.
Topics: Cochlea; Congenital Abnormalities; Deafness; Diiodotyrosine; Goiter; Hearing Loss; Humans; Iodine Is | 1964 |
Hearing loss and retarded cochlear development in mice lacking type 2 iodothyronine deiodinase.
Topics: Animals; Base Sequence; Cochlea; DNA, Complementary; Evoked Potentials, Auditory, Brain Stem; Hearin | 2004 |
Congenital hypothyroidism, dwarfism, and hearing impairment caused by a missense mutation in the mouse dual oxidase 2 gene, Duox2.
Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Base Sequence; Body Weight; Cochlea; Congenit | 2007 |
Mice deficient for the type II transmembrane serine protease, TMPRSS1/hepsin, exhibit profound hearing loss.
Topics: Animals; Auditory Threshold; Blotting, Western; Cochlea; Evoked Potentials, Auditory, Brain Stem; Ge | 2007 |
Deafness in myxoedema.
Topics: Adult; Aged; Female; Hearing Loss; Humans; In Vitro Techniques; Male; Middle Aged; Myxedema; Thyroxi | 1979 |