folic acid has been researched along with Bonnevie-Ullrich Syndrome in 3 studies
| 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 (33.33) | 24.3611 |
| 2020's | 2 (66.67) | 2.80 |
| Authors | Studies |
|---|---|
| Guo, QN; Liao, SX; Liu, ZY; Long, JG; Wang, HD; Wang, L | 1 |
| Abdulhalim, EN; El-Bassyouni, HT; Hamed, K; Hashem, SA; Kamel, SM; Khedr, AA; Youness, ER | 1 |
| Araújo, J; Bispo, AV; de Barros, JV; dos Santos, LO; Duarte, AR; Muniz, MT; Santos, N | 1 |
3 other study(ies) available for folic acid and Bonnevie-Ullrich Syndrome
| Article | Year |
|---|---|
Different effects of maternal homocysteine concentration, MTHFR and MTRR genetic polymorphisms on the occurrence of fetal aneuploidy.
Topics: Aneuploidy; Case-Control Studies; Female; Fetus; Flavoproteins; Folic Acid; Genotype; Homocysteine; Humans; Methylenetetrahydrofolate Reductase (NADPH2); Polymorphism, Genetic; Trisomy; Turner Syndrome | 2022 |
The role of the deficiency of vitamin B12 and folic acid on homocysteinemia in children with Turner syndrome.
Topics: Child; Folic Acid; Folic Acid Deficiency; Homocysteine; Humans; Hyperhomocysteinemia; Turner Syndrome; Vitamin B 12; Vitamin B 12 Deficiency | 2023 |
Polymorphisms in folate pathway genes are not associated with somatic nondisjunction in turner syndrome.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Cross-Sectional Studies; Cytogenetic Analysis; Folic Acid; Genotype; Humans; Logistic Models; Methylenetetrahydrofolate Reductase (NADPH2); Nondisjunction, Genetic; Odds Ratio; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Replication Protein C; Risk Factors; Signal Transduction; Thymidylate Synthase; Turner Syndrome | 2015 |