thyroxine has been researched along with Diseases in Twins in 18 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.
Diseases in Twins: Disorders affecting TWINS, one or both, at any age.
| Excerpt | Relevance | Reference |
|---|---|---|
| "All clinical and laboratory evidence of von Willebrand disease resolved transiently after infusion of desmopressin, and permanently with L-thyroxine therapy." | 5.29 | Acquired von Willebrand disease in twins with autoimmune hypothyroidism: response to desmopressin and L-thyroxine therapy. ( Bruggers, CS; McElligott, K; Rallison, ML, 1994) |
| "Maternal Graves' disease can, due to the presence of anti-thyroid stimulating hormone (TSH) receptor antibodies and the maternal use of anti-thyroid drugs, result in thyroid dysfunction in the neonate." | 1.33 | [Central congenital hypothyroidism due to Graves' disease in the mother]. ( de Mol, AC; Kempers, MJ; Liebrand, CA; Noordam, C, 2006) |
| "With the diagnosis of neonatal Graves' disease established, both twins were treated with propranolol (2 mg/kg." | 1.30 | [Neonatal Basedow's disease in twins from a mother with severe T3 hyperthyroidism]. ( Grüters, A; Hüfner, M; Lakomek, M; Roth, C; Siggelkow, H, 1997) |
| "All clinical and laboratory evidence of von Willebrand disease resolved transiently after infusion of desmopressin, and permanently with L-thyroxine therapy." | 1.29 | Acquired von Willebrand disease in twins with autoimmune hypothyroidism: response to desmopressin and L-thyroxine therapy. ( Bruggers, CS; McElligott, K; Rallison, ML, 1994) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 6 (33.33) | 18.7374 |
| 1990's | 5 (27.78) | 18.2507 |
| 2000's | 5 (27.78) | 29.6817 |
| 2010's | 2 (11.11) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Zwaveling-Soonawala, N | 1 |
| van Beijsterveldt, CE | 1 |
| Mesfum, ET | 1 |
| Wiedijk, B | 1 |
| Oomen, P | 1 |
| Finken, MJ | 1 |
| Boomsma, DI | 1 |
| van Trotsenburg, AS | 1 |
| Galbis Soto, S | 1 |
| Bahíllo Curieses, P | 1 |
| de la Huerga López, A | 1 |
| Martínez Sopena, MJ | 1 |
| Benvenga, S | 1 |
| Ordookhani, A | 1 |
| Pearce, EN | 1 |
| Tonacchera, M | 1 |
| Azizi, F | 1 |
| Braverman, LE | 1 |
| Narendran, P | 1 |
| Lado-Abeal, J | 1 |
| Moeller, LC | 1 |
| Refetoff, S | 1 |
| Liebrand, CA | 1 |
| de Mol, AC | 1 |
| Kempers, MJ | 1 |
| Noordam, C | 1 |
| Berghout, A | 1 |
| Peeters, RP | 1 |
| Kurtoglu, S | 1 |
| Keskin, M | 1 |
| Koklu, E | 1 |
| Akcakus, M | 1 |
| Atabek, ME | 1 |
| Hatipoglu, N | 1 |
| Young, JG | 1 |
| Kyprie, RM | 1 |
| Ross, NT | 1 |
| Cohen, DJ | 1 |
| Zakarija, M | 1 |
| De Forteza, R | 1 |
| McKenzie, JM | 1 |
| Ghandur-Mnaymneh, L | 1 |
| Bruggers, CS | 1 |
| McElligott, K | 1 |
| Rallison, ML | 1 |
| Chelimsky, G | 1 |
| Davis, ID | 1 |
| Kliegman, RM | 1 |
| Roth, C | 1 |
| Siggelkow, H | 1 |
| Grüters, A | 1 |
| Hüfner, M | 1 |
| Lakomek, M | 1 |
| Klein, AH | 1 |
| Stinson, D | 1 |
| Foley, B | 1 |
| Larsen, PR | 1 |
| Foley, TP | 1 |
| Traisman, ES | 1 |
| Traisman, HS | 1 |
| Fiorillo, A | 1 |
| Farina, V | 1 |
| DiMaio, S | 1 |
| Ciriaco, M | 1 |
| Nunziata, L | 1 |
| Scippa, L | 1 |
| D'Agostino, N | 1 |
| Mandel, SH | 1 |
| Hanna, CE | 1 |
| LaFranchi, SH | 1 |
| Sperling, MA | 1 |
| Wolfsen, AR | 1 |
| Fisher, DA | 1 |
| Dynski-Klein, M | 1 |
2 reviews available for thyroxine and Diseases in Twins
| Article | Year |
|---|---|
Partial thyroxine-binding globulin (TBG) deficiency in a family with no detectable mutation of the TBG gene.
Topics: Adult; Chromosomes, Human, X; Diseases in Twins; Dosage Compensation, Genetic; Female; Humans; Male; | 2003 |
Neonatal hyponatremia associated with congenital hypothyroidism.
Topics: Adult; Animals; Congenital Hypothyroidism; Diseases in Twins; Female; Humans; Hyponatremia; Hypothyr | 1997 |
16 other studies available for thyroxine and Diseases in Twins
| Article | Year |
|---|---|
Fetal Environment Is a Major Determinant of the Neonatal Blood Thyroxine Level: Results of a Large Dutch Twin Study.
Topics: Diseases in Twins; Environment; Female; Fetal Development; Genetic Predisposition to Disease; Humans | 2015 |
[False negative in the first neonatal screening for congenital hypothyroidism in a newborn twin].
Topics: Congenital Hypothyroidism; Delayed Diagnosis; Diseases in Twins; False Negative Reactions; Female; F | 2016 |
Detection of circulating autoantibodies against thyroid hormones in an infant with permanent congenital hypothyroidism and her twin with transient congenital hypothyroidism: possible contribution of thyroid hormone autoantibodies to neonatal and infant hy
Topics: Autoantibodies; Autoantigens; Body Height; Body Weight; Child, Preschool; Congenital Hypothyroidism; | 2008 |
[Central congenital hypothyroidism due to Graves' disease in the mother].
Topics: Adult; Congenital Hypothyroidism; Diseases in Twins; Female; Graves Disease; Humans; Infant, Newborn | 2006 |
[Central congenital hypothyroidism due to Graves' disease in the mother].
Topics: Biomarkers; Congenital Hypothyroidism; Diseases in Twins; Female; Graves Disease; Humans; Pregnancy; | 2007 |
Congenital goiter in premature twins due to propylthiouracil treatment.
Topics: Congenital Hypothyroidism; Diseases in Twins; Female; Graves Disease; Humans; Infant, Newborn; Male; | 2007 |
Serum dopamine-beta-hydroxylase activity: clinical applications in child psychiatry.
Topics: Adolescent; Adult; Age Factors; Aphasia; Autistic Disorder; Child; Diseases in Twins; Dopamine beta- | 1980 |
Characteristics and clinical correlates of a novel thyroid-stimulating autoantibody.
Topics: Adult; Animals; Antibody Specificity; Autoimmune Diseases; CHO Cells; Congenital Hypothyroidism; Cri | 1994 |
Acquired von Willebrand disease in twins with autoimmune hypothyroidism: response to desmopressin and L-thyroxine therapy.
Topics: Adolescent; Deamino Arginine Vasopressin; Diseases in Twins; Drug Therapy, Combination; Female; Huma | 1994 |
[Neonatal Basedow's disease in twins from a mother with severe T3 hyperthyroidism].
Topics: Adrenergic beta-Antagonists; Adult; Antithyroid Agents; Autoantibodies; Developmental Disabilities; | 1997 |
Thyroid function studies in preterm infants recovering from the respiratory distress syndrome.
Topics: Convalescence; Diseases in Twins; Gestational Age; Humans; Hypothyroidism; Infant; Infant, Newborn; | 1977 |
Hyperthyroidism in identical adolescent male twins.
Topics: Adolescent; Antithyroid Agents; Chicago; Child; Diseases in Twins; Humans; Hyperthyroidism; Male; Ph | 1990 |
Myocardial dysfunction in two hypothyroid twins with thalassaemia major.
Topics: Child; Diseases in Twins; Echocardiography; Humans; Hypothyroidism; Male; Myocardial Contraction; Th | 1989 |
Diminished thyroid-stimulating hormone secretion associated with neonatal thyrotoxicosis.
Topics: Diseases in Twins; Humans; Infant, Newborn; Male; Propylthiouracil; Thyrotoxicosis; Thyrotropin; Thy | 1986 |
Congenital adrenal hypoplasia: an isolated defect of organogenesis.
Topics: 17-Ketosteroids; Adrenal Gland Diseases; Adrenal Glands; Adrenocorticotropic Hormone; Aldosterone; B | 1973 |
[Temporary hypofunction of the thyroid gland in one non-identical twin].
Topics: Adult; Birth Weight; Child; Congenital Hypothyroidism; Diseases in Twins; Female; Humans; Hypothyroi | 1968 |