homocysteine has been researched along with Congenital Limb Deformities in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Carmichael, SL; Cheng, S; Finnell, RH; Iovannisci, DM; Lammer, EJ; Shaw, GM; Yang, W | 1 |
Hunter, AG | 1 |
2 other study(ies) available for homocysteine and Congenital Limb Deformities
Article | Year |
---|---|
Risks of human limb deficiency anomalies associated with 29 SNPs of genes involved in homocysteine metabolism, coagulation, cell-cell interactions, inflammatory response, and blood pressure regulation.
Topics: Blood Coagulation; Blood Pressure; Case-Control Studies; Cell Communication; Female; Genotype; Homocysteine; Humans; Infant, Newborn; Inflammation; Limb Deformities, Congenital; Male; Maternal-Fetal Exchange; Odds Ratio; Polymorphism, Single Nucleotide; Pregnancy; Risk Factors; Smoking; Vitamins | 2006 |
A pilot study of the possible role of familial defects in anticoagulation as a cause for terminal limb reduction malformations.
Topics: Antibodies, Anticardiolipin; Antithrombin III; Factor V; Female; Homocysteine; Humans; Limb Deformities, Congenital; Male; Methylenetetrahydrofolate Reductase (NADPH2); Mothers; Mutation; Oxidoreductases Acting on CH-NH Group Donors; Pilot Projects; Polymorphism, Genetic; Protein C; Protein S; Thrombophilia | 2000 |