Within the last few years, knowledge about vitamins has increased dramatically. This new
edition of a bestseller presents comprehensive summaries that analyze the chemical …

Background Methylenetetrahydrofolate reductase (MTHFR) plays a crucial role in the
hyperhomocysteinemia, which is a risk factor related to the occurrence of congenital heart …

The aim of our study was to evaluate the association between polymorphisms in the
methylenetetrahydrofolate reductase (MTHFR) gene and the risk for congenital heart …

Congenital heart disease is one of the most common congenital malformations and thus
represents a considerable public health burden. Hence, the identification of individuals and …

Abstract Background/Aims: Published studies indicated that the MTHFR gene
polymorphisms C677T and A1298C are associated with congenital heart disease (CHD) risk …

The Roles of Reduced Folate Carrier-1 (RFC1) A80G (rs1051266) Polymorphism in Congenital
Heart Disease: A Meta-Analysis - PMC Back to Top Skip to main content NIH NLM Logo Access …

Background Congenital heart disease (CHD) is one of the most common birth defects and
the leading cause of deaths among individuals with congenital structural abnormalities …

Many published studies have evaluated the association between the 5, 10-
methylenetetrahydrofolate reductase (MTHFR) C677T (rs1801133) polymorphism and the …

Objective To evaluate whether the association between maternal periconceptional use of
selective serotonin reuptake inhibitors (SSRIs) and increased risk of congenital heart defects …

Background. Congenital heart defect (CHD) is one of the most common birth defects in the
world. The methylenetetrahydrofolate reductase (MTHFR) and methionine synthase …