coumarin has been researched along with von Willebrand Diseases in 1 studies
2H-chromen-2-one: coumarin derivative
von Willebrand Diseases: Group of hemorrhagic disorders in which the VON WILLEBRAND FACTOR is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII, and impaired platelet adhesion.
| 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 |
|---|---|
| KAPPELER, R | 1 |
1 other study available for coumarin and von Willebrand Diseases
| Article | Year |
|---|---|
[The reaction of factor V in the serum under normal and pathological conditions].
Topics: Blood Coagulation; Blood Coagulation Tests; Coumarins; Factor V; Hemophilia A; Prothrombin Time; von | 1955 |