thyroxine has been researched along with Albright Syndrome in 5 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 |
|---|---|---|
| " Thyroid crisis is even rare in patients with MAS, and we report the clinical outcomes of the first case of a MAS patient with atypical triiodothyronine (T3) hyperthyroidism who developed thyroid crisis after orthopedic surgery." | 8.12 | Postoperative thyroid crisis in an 11-year old male with McCune-Albright syndrome and atypical triiodothyronine hyperthyroidism: A case report. ( Hu, C; Hu, J, 2022) |
| "A 17-year-old girl with McCune-Albright syndrome (MAS) was suspected of having central hypothyroidism based on an inappropriately normal thyroid-stimulating hormone (TSH) and low free thyroxine (fT4)." | 7.81 | Low serum free thyroxine level in a girl with McCune-Albright syndrome. ( Pajuväli, A; Peet, A; Roosimaa, M; Tillmann, V, 2015) |
| " Thyroid crisis is even rare in patients with MAS, and we report the clinical outcomes of the first case of a MAS patient with atypical triiodothyronine (T3) hyperthyroidism who developed thyroid crisis after orthopedic surgery." | 4.12 | Postoperative thyroid crisis in an 11-year old male with McCune-Albright syndrome and atypical triiodothyronine hyperthyroidism: A case report. ( Hu, C; Hu, J, 2022) |
| "A 17-year-old girl with McCune-Albright syndrome (MAS) was suspected of having central hypothyroidism based on an inappropriately normal thyroid-stimulating hormone (TSH) and low free thyroxine (fT4)." | 3.81 | Low serum free thyroxine level in a girl with McCune-Albright syndrome. ( Pajuväli, A; Peet, A; Roosimaa, M; Tillmann, V, 2015) |
| "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 (20.00) | 18.7374 |
| 1990's | 1 (20.00) | 18.2507 |
| 2000's | 1 (20.00) | 29.6817 |
| 2010's | 1 (20.00) | 24.3611 |
| 2020's | 1 (20.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hu, J | 1 |
| Hu, C | 1 |
| Roosimaa, M | 1 |
| Pajuväli, A | 1 |
| Peet, A | 1 |
| Tillmann, V | 1 |
| Pohlenz, J | 1 |
| Ahrens, W | 1 |
| Hiort, O | 1 |
| Lightner, ES | 1 |
| Penny, R | 1 |
| Frasier, SD | 1 |
| Feuillan, PP | 1 |
| Shawker, T | 1 |
| Rose, SR | 1 |
| Jones, J | 1 |
| Jeevanram, RK | 1 |
| Nisula, BC | 1 |
5 other studies available for thyroxine and Albright Syndrome
| Article | Year |
|---|---|
Postoperative thyroid crisis in an 11-year old male with McCune-Albright syndrome and atypical triiodothyronine hyperthyroidism: A case report.
Topics: Child; Femur; Fibrous Dysplasia, Polyostotic; Humans; Hyperthyroidism; Male; Postoperative Complicat | 2022 |
Low serum free thyroxine level in a girl with McCune-Albright syndrome.
Topics: Adolescent; Female; Fibrous Dysplasia, Polyostotic; Humans; Hyperthyroidism; Hypothyroidism; Thyroxi | 2015 |
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 |
Growth hormone excess and sexual precocity in polyostotic fibrous dysplasia (McCune-Albright syndrome): evidence for abnormal hypothalamic function.
Topics: Blood Glucose; Child, Preschool; Estradiol; Fibrous Dysplasia of Bone; Fibrous Dysplasia, Polyostoti | 1975 |
Thyroid abnormalities in the McCune-Albright syndrome: ultrasonography and hormonal studies.
Topics: Adolescent; Child; Child, Preschool; Female; Fibrous Dysplasia, Polyostotic; Humans; Thyroid Disease | 1990 |