4-azido-7-phenylpyrazolo-(1,5a)-1,3,5-triazine has been researched along with von Willebrand Diseases in 1 studies
*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. [MeSH]
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Joseph, D; Watts, JC | 1 |
1 other study(ies) available for 4-azido-7-phenylpyrazolo-(1,5a)-1,3,5-triazine and von Willebrand Diseases
| Article | Year |
|---|---|
Difficulty of establishing preoperative coagulation status.
Topics: Blood Coagulation Tests; Humans; Male; Preoperative Care; Triazines; von Willebrand Diseases; Young Adult | 2011 |