aldosterone has been researched along with Wolfram Syndrome in 1 studies
Wolfram Syndrome: A hereditary condition characterized by multiple symptoms including those of DIABETES INSIPIDUS; DIABETES MELLITUS; OPTIC ATROPHY; and DEAFNESS. This syndrome is also known as DIDMOAD (first letter of each word) and is usually associated with VASOPRESSIN deficiency. It is caused by mutations in gene WFS1 encoding wolframin, a 100-kDa transmembrane protein.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (100.00) | 2.80 |
| Authors | Studies |
|---|---|
| Punapart, M | 1 |
| Seppa, K | 1 |
| Jagomäe, T | 1 |
| Liiv, M | 1 |
| Reimets, R | 1 |
| Kirillov, S | 1 |
| Kaasik, A | 1 |
| Moons, L | 1 |
| De Groef, L | 1 |
| Terasmaa, A | 1 |
| Vasar, E | 1 |
| Plaas, M | 1 |
1 other study available for aldosterone and Wolfram Syndrome
| Article | Year |
|---|---|
The Expression of RAAS Key Receptors,
Topics: Aldosterone; Animals; Calmodulin-Binding Proteins; Cells, Cultured; Disease Models, Animal; Down-Reg | 2021 |