valine has been researched along with Thrombocytopathy in 1 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Cloutier, S; Duan, Z; Jackson, SC; Poon, MC; Rand, ML; Sinclair, GD | 1 |
1 other study(ies) available for valine and Thrombocytopathy
Article | Year |
---|---|
The Montreal platelet syndrome kindred has type 2B von Willebrand disease with the VWF V1316M mutation.
Topics: Amino Acid Substitution; Blood Coagulation Tests; Blood Platelet Disorders; Blood Platelets; DNA Mutational Analysis; Family; Female; Humans; Male; Methionine; Mutation, Missense; Pedigree; Platelet Aggregation; Syndrome; Valine; von Willebrand Diseases; von Willebrand Factor | 2009 |