adenine has been researched along with Cretinism in 2 studies
| 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 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| 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 |
| Michelangeli, VP | 1 |
| Poon, CW | 1 |
| Arnus, EE | 1 |
| Frauman, AG | 1 |
| Connelly, J | 1 |
| Colman, PG | 1 |
2 other studies available for adenine and Cretinism
| Article | Year |
|---|---|
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 |
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 |