thymine has been researched along with Pseudohypoaldosteronism in 1 studies
Pseudohypoaldosteronism: A heterogeneous group of disorders characterized by renal electrolyte transport dysfunctions. Congenital forms are rare autosomal disorders characterized by neonatal hypertension, HYPERKALEMIA, increased RENIN activity and ALDOSTERONE concentration. The Type I features HYPERKALEMIA with sodium wasting; Type II, HYPERKALEMIA without sodium wasting. Pseudohypoaldosteronism can be the result of a defective renal electrolyte transport protein or acquired after KIDNEY TRANSPLANTATION.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Riepe, FG | 1 |
| Krone, N | 1 |
| Morlot, M | 1 |
| Peter, M | 1 |
| Sippell, WG | 1 |
| Partsch, CJ | 1 |
1 other study available for thymine and Pseudohypoaldosteronism
| Article | Year |
|---|---|
Autosomal-dominant pseudohypoaldosteronism type 1 in a Turkish family is associated with a novel nonsense mutation in the human mineralocorticoid receptor gene.
Topics: Base Sequence; Codon, Nonsense; Codon, Terminator; Cytosine; Exons; Genes, Dominant; Heterozygote; H | 2004 |