aldosterone has been researched along with Purpura, Thrombotic Thrombocytopenic in 1 studies
Purpura, Thrombotic Thrombocytopenic: An acquired, congenital, or familial disorder caused by PLATELET AGGREGATION with THROMBOSIS in terminal arterioles and capillaries. Clinical features include THROMBOCYTOPENIA; HEMOLYTIC ANEMIA; AZOTEMIA; FEVER; and thrombotic microangiopathy. The classical form also includes neurological symptoms and end-organ damage, such as RENAL FAILURE. Mutations in the ADAMTS13 PROTEIN gene have been identified in familial cases.
| 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 |
|---|---|
| Frey, FJ | 1 |
1 review available for aldosterone and Purpura, Thrombotic Thrombocytopenic
| Article | Year |
|---|---|
[Nephrology 1999: substantial Swiss contributions].
Topics: Aldosterone; Hemolytic-Uremic Syndrome; Humans; Nephrology; Purpura, Thrombotic Thrombocytopenic; Sw | 2000 |