coumarin has been researched along with Factor X Deficiency in 1 studies
2H-chromen-2-one: coumarin derivative
Factor X Deficiency: Blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired. It is characterized by defective activity in both the intrinsic and extrinsic pathways, impaired thromboplastin time, and impaired prothrombin consumption.
| 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 |
|---|---|
| Girolami, A | 1 |
| Ruzza, G | 1 |
| Cappellato, MG | 1 |
| Vicarioto, MA | 1 |
1 other study available for coumarin and Factor X Deficiency
| Article | Year |
|---|---|
Factor X antigen evaluation by means of a laser nephelometer in health and disease.
Topics: Adult; Antigens; Coumarins; Factor X; Factor X Deficiency; Female; Heterozygote; Homozygote; Humans; | 1985 |