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

Methylenetetrahydrofolate reductase gene C677T mutation and plasma homocysteine level in Behçet's disease.

Rheumatology international - 1 Sept 2003

Canataroglu Abdullah, Tanriverdi Kahraman, Inal Tamer, Seydaoglu Gulsah, Arslan Didem, Ozbek Suleyman, Baslamisli Fikri

Abstract excerpt

OBJECTIVE: The aim of this study was to assess whether homozygosity for the 5, 10-methylenetetrahydrofolate reductase (MTHFR) C677T mutation and plasma homocysteine concentration are related to deep vein thrombosis in Behçet's disease (BD) patients. METHODS: Forty BD patients (23 males, 17 females; mean age 40.2+/-8.4 years) and 60 healthy controls (HC) (34 males, 26 females; mean age 41.6+/-6.9 years) were...

Read the complete abstract on PubMed

Topics

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

Share to Behcet Syndrome
Share to MTHFR gene

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Homocysteine

Share to Homozygote

Share to Methylenetetrahydrofolate Reductase (NADPH2)

Share to Mutation

Share to Venous Thrombosis

Source

Identifiers

PMID: 14504916
DOI: 10.1007/s00296-003-0301-8

Genes

MTHFR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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

Methylenetetrahydrofolate reductase gene C677T mutation and plasma homocysteine level in Behçet's disease.PMID 14504916Read ↗

Effects of factor V gene G1691A, methylenetetrahydrofolate reductase gene C677T, and prothombin gene G20210A mutations on deep venous thrombogenesis in Behçet's disease.Semantic proximity Read ↗

Thymidylate synthase genotype and serum concentrations of homocysteine and folate in Behçet's disease.Semantic proximity Read ↗

5,10-Methylenetetrahydrofolate reductase C677T gene polymorphism in Behcet's patients with or without ocular involvement.Semantic proximity Read ↗

Clinical significance of determining plasma homocysteine: case-control study on arterial and venous thrombotic patients.Semantic proximity Read ↗

Methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and variations of homocysteine concentrations in patients with Behcet's disease.Semantic proximity Read ↗

[Study on the association of polymorphisms in homocysteine metabolism related enzymes with deep venous thrombosis].Semantic proximity Read ↗

Hyperhomocysteinemia and the MTHFR C677T mutation in Budd-Chiari syndrome.Semantic proximity Read ↗

Influence of methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism, B vitamins and other factors on plasma homocysteine and risk of thromboembolic disease in Chinese.Semantic proximity Read ↗

Factor V Leiden mutation in patients with Behçet's disease.Semantic proximity Read ↗

Association of allelic variants of factor V Leiden, prothrombin and methylenetetrahydrofolate reductase with thrombosis or ocular involvement in Behçet's disease: a systematic review and meta-analysis.Semantic proximity Read ↗

Homocysteine, MTHFR and risk of venous thrombosis: a meta-analysis of published epidemiological studies.Semantic proximity Read ↗

C677T methylenetetrahydrofolate reductase gene polymorphism as a risk factor involved in venous thromboembolism: a population-based case-control study.Semantic proximity Read ↗

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