homocystine has been researched along with Antithrombin 3 Deficiency in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (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 |
---|---|
Newman, R | 1 |
Bernardi, F; Coccheri, S; Ferraresi, P; Grauso, F; Grossi, G; Legnani, C; Marchetti, G; Palareti, G; Piazzi, S; Sassi, S | 1 |
2 other study(ies) available for homocystine and Antithrombin 3 Deficiency
Article | Year |
---|---|
Laboratory work-up of patients with heritable thrombotic disorders.
Topics: Adult; Antithrombin III Deficiency; Disease Susceptibility; Female; Genetic Predisposition to Disease; Homocystine; Humans; Male; Pregnancy; Protein C Deficiency; Protein S Deficiency; Thrombosis | 1997 |
Hyperhomocyst(e)inemia and a common methylenetetrahydrofolate reductase mutation (Ala223Val MTHFR) in patients with inherited thrombophilic coagulation defects.
Topics: Adult; Aged; Antithrombin III; Antithrombin III Deficiency; Disease Susceptibility; Enzyme Activation; Factor V; Gene Frequency; Genotype; Homocysteine; Homocystine; Humans; Italy; Male; Methylenetetrahydrofolate Reductase (NADPH2); Middle Aged; Oxidoreductases Acting on CH-NH Group Donors; Point Mutation; Protein C; Protein S Deficiency; Risk Factors; Thrombophilia | 1997 |