Folates, vitamin B12, homocystein and neural tube defects;Folates, vitamine B12, homocystéine et anomalies du tube neural

Annales de Biologie Clinique

Volumn 59, Issue 1, 2001, Pages 111-112

  Candito, M ^a   Van Obberghen, E ^a  

^a PASTEUR HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CYANOCOBALAMIN; FOLIC ACID; HOMOCYSTEINE; METHIONINE SYNTHASE; METHYLENETETRAHYDROFOLATE DEHYDROGENASE;

CYANOCOBALAMIN DEFICIENCY; FOLIC ACID DEFICIENCY; GENE ISOLATION; HUMAN; HUMAN CELL; HUMAN TISSUE; HYPERHOMOCYSTEINEMIA; NEURAL TUBE DEFECT; SHORT SURVEY; VITAMIN DEFICIENCY; VITAMIN INTAKE;

FOLIC ACID DEFICIENCY; HOMOCYSTEINE; HUMANS; NEURAL TUBE DEFECTS; VITAMIN B 12 DEFICIENCY;

EID: 0035132618     PISSN: 00033898     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Short Survey

References (27)

1. Heterogenity of neural tube defects in Europe: The significance of site of defect and presence of other major anomalies in relation to geographic differences in prevalence
2. Folic acid metabolism and human embryopathy
3. Homocysteine metabolism in pregnancies complicated by neural-tube defects
4. Maternal plasma folate and vitamin B12 are independent risk factors for neural tube detects
5. Prevention of neural tube defects: Results of the Medical Research Council Vitamin Study
6. Prevention of the first occurrence of neural-tube defects periconceptional vitamin supplementation
7. Maternal hyperhomocysteinemia: A risk factor for neural tube defects?
8. Uptake and utilization of DL-5-methyl 14C tetrahydropteroylmonoglutamate by cultured cytotrophoblasts associated with neural tube detects
9. Molecular genetic analysis of human folate receptors in neural tube defects
10. Les transporteurs des folates: Analyse génétique et relation avec l'homocystéine plasmatique chez le sujet sain
11. Amniotic fluid B12 and folate levels associated with neural tube defects
12. Neural-tube defects are associated with low concentrations of cobalamin in amniotic fluid
13. Elevated midtrimester serum methylmalonic acid levels as a risk factor for neural tube defects
14. Homocysteine and marginal vitamin deficiency
15. Plasma homocysteine before and after methionine loading with regard to age, gender, and menopausal status
16. Risk factors for neural tube defects: Analysis of common genetic variants of methylenetetrahydrofolate reductase and cystathione β-synthase
17. Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders
18. Genetic causes of mild hyperhomocysteinemia in patients with premature occlusive coronary artery diseases
19. Methionine synthase D919G polymorphism is a significant but modest determinant of circulating homocysteine concentrations
20. SSCP analysis of the human methylenetetrahydrofolate deshydrogenase gene: Relevance to neural tube defects
21. Molecular genetic analysis of the gene encoding the trifunctional enzyme MTHFD in patients with neural tube defects
22. A common variant in methionine synthase reductase combined with low cobalamin (vitamine B12) increases risk for spina bifida
23. Reduction of plasma homocysteine levels by breakfast cereal fortified with folic acid in patients with coronary heart disease
24. The effect of folic acid fortification on plasma folate and total homocysteine concentrations
25. Neural-tube defects and derangement of homocysteine metabolism
26. The implication of genetic diversity for nutrient requirements: The case of folate
27. Génétique moléculaire de la reméthylation de l'homocystéine