iproniazid has been researched along with IgA Vasculitis in 1 studies
IgA Vasculitis: A systemic non-thrombocytopenic purpura caused by HYPERSENSITIVITY VASCULITIS and deposition of IGA-containing IMMUNE COMPLEXES within the blood vessels throughout the body, including those in the kidney (KIDNEY GLOMERULUS). Clinical symptoms include URTICARIA; ERYTHEMA; ARTHRITIS; GASTROINTESTINAL HEMORRHAGE; and renal involvement. Most cases are seen in children after acute upper respiratory infections.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (100.00) | 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 | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| BISIANI, M | 1 |
| FRESIA, P | 1 |
| GENOVESE, E | 1 |
| MORTARI, A | 1 |
1 other study available for iproniazid and IgA Vasculitis
| Article | Year |
|---|---|
[Capacity of iproniazid to inhibit in vivo the coronary constrictor effect of pitressin].
Topics: Antidiuretic Hormone Receptor Antagonists; Coronary Stenosis; Coronary Vessels; Humans; IgA Vasculit | 1958 |