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

Homocysteine, folate, lipid profile and MTHFR genotype and disability in children with myelomeningocele.

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery - 1 Oct 2006

Rendeli Claudia, Ausili Emanuele, Castorina Mario, Antuzzi Daniela, Tabacco Fabrizia, Caldarelli Massimo

Abstract excerpt

STUDY DESIGN: We performed a cross-sectional study in myelomeningocele children. OBJECTIVE: To investigate plasma total homocysteine, folate, lipid profile, 5,10- metylenetetrahydrofolate reductase genotype (MTHFR) and disability. MATERIALS AND METHODS: Sixty patients aged between 2 and 14 years with myelomeningocele (18 ambulatory and 42 non-ambulatory) and 150 healthy children of same age, are investigated for...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Child

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Child, Preschool

Share to Folic Acid

Share to Homocysteine

Share to Lipids

Share to Methylenetetrahydrofolate Reductase (NADPH2)

Share to Sex Factors

Source

Identifiers

PMID: 16602021
DOI: 10.1007/s00381-006-0056-0

Genes

MTHFR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Homocysteine, folate, lipid profile and MTHFR genotype and disability in children with myelomeningocele.PMID 16602021Read ↗

Overview of homocysteine and folate metabolism. With special references to cardiovascular disease and neural tube defectsSemantic proximity Read ↗

The effect of C677T mutation of methylene tetrahydrofolate reductase gene and plasma folate level on hyperhomocysteinemia in patients with meningomyelocele.Semantic proximity Read ↗

Manifestations of neurological symptoms and thromboembolism in adults with MTHFR-deficiency.Semantic proximity Read ↗

Guidelines for diagnosis and management of the cobalamin‐related remethylation disorders cblC, cblD, cblE, cblF, cblG, cblJ and MTHFR deficiencySemantic proximity Read ↗

Metabolic and genetic risk factors for migraine in children.Semantic proximity Read ↗

[Methylenetetrahydrofolate reductase polymorphisms as risk factors for myelomeningocele].Semantic proximity Read ↗

Folate metabolism gene 5,10-methylenetetrahydrofolate reductase (MTHFR) is associated with ADHD in myelomeningocele patients.Semantic proximity Read ↗

Myelomeningocele among Pakistani population.Semantic proximity Read ↗

Maternal gene-micronutrient interactions related to one-carbon metabolism and the risk of myelomeningocele among offspring.Semantic proximity Read ↗

Evidence of gene-gene interactions between MTHFD1 and MTHFR in relation to anterior encephalocele susceptibility in Northeast India.Semantic proximity Read ↗

Folate and vitamin B12-related genes and risk for omphalocele.Semantic proximity Read ↗

Assessment of homocysteine statusSemantic proximity Read ↗

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