coumarin has been researched along with IgA Vasculitis in 1 studies
2H-chromen-2-one: coumarin derivative
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.
Excerpt | Relevance | Reference |
---|---|---|
"We present 2 cases of homozygous protein C deficiency with ocular and extraocular manifestation." | 1.30 | Ophthalmic manifestation of congenital protein C deficiency. ( Beeg, T; Hattenbach, LO; Kreuz, W; Zubcov, A, 1999) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (100.00) | 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 |
---|---|
Hattenbach, LO | 1 |
Beeg, T | 1 |
Kreuz, W | 1 |
Zubcov, A | 1 |
1 other study available for coumarin and IgA Vasculitis
Article | Year |
---|---|
Ophthalmic manifestation of congenital protein C deficiency.
Topics: Anticoagulants; Cataract; Consanguinity; Coumarins; Eye Diseases; Female; Humans; IgA Vasculitis; In | 1999 |