adenine has been researched along with Hypothyroidism in 5 studies
Hypothyroidism: A syndrome that results from abnormally low secretion of THYROID HORMONES from the THYROID GLAND, leading to a decrease in BASAL METABOLIC RATE. In its most severe form, there is accumulation of MUCOPOLYSACCHARIDES in the SKIN and EDEMA, known as MYXEDEMA. It may be primary or secondary due to other pituitary disease, or hypothalamic dysfunction.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Isolated TSH deficiency is a rare cause of congenital hypothyroidism." | 1.32 | Four new cases of congenital secondary hypothyroidism due to a splice site mutation in the thyrotropin-beta gene: phenotypic variability and founder effect. ( Aumann, U; Borck, G; Koch, G; Korsch, E; Martiné, U; Onenli-Mungan, N; Ozer, G; Pfäffle, R; Pohlenz, J; Refetoff, S; Scherberg, NH; Topaloglu, AK; Wildhardt, G; Yuksel, B, 2004) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (20.00) | 18.7374 |
| 1990's | 1 (20.00) | 18.2507 |
| 2000's | 2 (40.00) | 29.6817 |
| 2010's | 1 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kang, IN | 1 |
| Musa, M | 1 |
| Harun, F | 1 |
| Junit, SM | 1 |
| Borck, G | 1 |
| Topaloglu, AK | 1 |
| Korsch, E | 1 |
| Martiné, U | 1 |
| Wildhardt, G | 1 |
| Onenli-Mungan, N | 1 |
| Yuksel, B | 1 |
| Aumann, U | 1 |
| Koch, G | 1 |
| Ozer, G | 1 |
| Pfäffle, R | 1 |
| Scherberg, NH | 1 |
| Refetoff, S | 1 |
| Pohlenz, J | 1 |
| Blunt, BC | 1 |
| Chen, Y | 1 |
| Potter, JD | 1 |
| Hofmann, PA | 1 |
| Michelangeli, VP | 1 |
| Poon, CW | 1 |
| Arnus, EE | 1 |
| Frauman, AG | 1 |
| Connelly, J | 1 |
| Colman, PG | 1 |
| Pakkenberg, H | 1 |
| Ford, DH | 1 |
| Rhines, R | 1 |
| Israely, RA | 1 |
5 other studies available for adenine and Hypothyroidism
| Article | Year |
|---|---|
Characterization of mutations in the FOXE1 gene in a cohort of unrelated Malaysian patients with congenital hypothyroidism and thyroid dysgenesis.
Topics: Adenine; Amino Acid Sequence; Animals; Cohort Studies; Congenital Abnormalities; DNA Primers; Forkhe | 2010 |
Four new cases of congenital secondary hypothyroidism due to a splice site mutation in the thyrotropin-beta gene: phenotypic variability and founder effect.
Topics: Adenine; Child; Child, Preschool; Congenital Hypothyroidism; Female; Founder Effect; Guanine; Haplot | 2004 |
Modest actomyosin energy conservation increases myocardial postischemic function.
Topics: Actomyosin; Adenine; Adenosine Triphosphatases; Adenosine Triphosphate; Animals; Calcium; Creatine; | 2005 |
Measurement of TSH receptor blocking immunoglobulins using 3H-adenine incorporation into FRTL-5 and JPO9 cells: use in a child with neonatal hypothyroidism.
Topics: Adenine; Antibodies; Binding, Competitive; Biological Assay; Cell Line; Congenital Hypothyroidism; F | 1995 |
Adenine-H3 uptake in nervous tissue, including regenerating nerve cells, as compared with other tissues in euthyroid, hypo- and hyperthyroid male rats.
Topics: Adenine; Adrenal Glands; Animals; Autoradiography; Bile; Brain; Chromatography; Hyperthyroidism; Hyp | 1965 |