Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Central nervous system malformations and the presence of the MTHFR-C677T mutation in fetal blood].

Revista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e Obstetricia - 1 Oct 2013

Simoni Renata Zaccaria, Couto Egle, Barini Ricardo, Heinrich-Moçouçah Juliana, Bragança Welbe Oliveira, Couto Evelyn Regina, Bizzachi Joyce Maria Annichino

Abstract excerpt

PURPOSE: To evaluate the association between central nervous system (CNS) malformations and the C677T-MTHFR mutation in fetal blood. METHODS: A case-control study was conducted to compare the MTHFR-C677T mutation detected in 78 fetuses with CNS malformations and with 100 morphologically normal fe...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Case-Control Studies
Share to Central Nervous System

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Fetal Blood

Share to MTHFR gene

Share to Methylenetetrahydrofolate Reductase (NADPH2)

Share to Mutation

Share to Nervous System Malformations

Share to Pregnancy

Source

Identifiers

PMID: 24337054
DOI: 10.1590/s0100-72032013001000002

Genes

MTHFR

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24337054-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Central nervous system malformations and the presence of the MTHFR-C677T mutation in fetal blood].PMID 24337054Read ↗

Cerebral ultrasound abnormalities in offsprings of women with C677T homozygous mutation in the MTHFR gene: a prospective study.Semantic proximity Read ↗

Analysis of MTHFR 1298A>C in addition to MTHFR 677C>T polymorphism as a risk factor for neural tube defects in the Turkish population.Semantic proximity Read ↗

[C677T and A1298C MTHFR polymorphisms in the etiology of neural tube defects in Spanish population].Semantic proximity Read ↗

[C677T polymorphism of the methylentetrahydrofolate reductase gene in mothers of children affected with neural tube defects].Semantic proximity Read ↗

Association between the MTHFR (rs1801133) gene variation and serum trace elements levels (Copper and Zinc) in individuals diagnosed with neural tube defects.Semantic proximity Read ↗

Association between Fetal MTHFR A1298C (rs1801131) Polymorphism and Neural Tube Defects Risk: A Systematic Review and Meta-Analysis.Semantic proximity Read ↗

Polymorphisms in folate-metabolizing genes and risk of having an offspring with congenital anomalies in the West Siberian region of Russia: a case-control study.Semantic proximity Read ↗

Genetic Profiling of Idiopathic Antenatal Intracranial Haemorrhage: What We Know?Semantic proximity Read ↗

[Methylene tetrahydrofolate reductase mutations as genetic risk factors for neural tube defects (NTF)].Semantic proximity Read ↗

[Meta analysis on the association between parental 5,10-methylenetetrahydrofolate reductase C677T polymorphism and the neural tube defects of their offspring].Semantic proximity Read ↗

MTHFR Gene Polymorphisms and DNA Methylation in Idiopathic Spontaneous Preterm Birth.Semantic proximity Read ↗

[Meta-analysis on relationship between the Chinese maternal MTHFR gene polymorphism(C677T) and neural tube defects in offspring].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.