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

Factor V (His 1299 Arg) in young Turkish patients with cerebral infarct.

Haemostasis - 1 Jan 2000

Akar N, Yilmaz E, Akar E, Deda G, Sipahi T

Abstract excerpt

Inherited gene defects related to the coagulation system have been reported as risk factors for stroke. Recently, a genetic component in the factor V (FV) gene that contributes to activated protein C resistance both in the presence and absence of FV 1691 G-->A was reported. This highly conserved FV gene haplotype was marked as R2 polymorphism, an A to G alteration at position 4070 in exon 13 that predicts the His...

Read the complete abstract on PubMed

Topics

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

Share to Cerebral Infarction
Share to Factor V
Share to Homozygote

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Incidence

Share to Infant

Share to Mutation, Missense

Share to Odds Ratio

Share to Turkey

Source

Identifiers

PMID: 11014961
DOI: 10.1159/000022533

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

Factor V (His 1299 Arg) in young Turkish patients with cerebral infarct.PMID 11014961Read ↗

Factor V1691 G-A, prothrombin 20210 G-A, and methylenetetrahydrofolate reductase 677 C-T variants in Turkish children with cerebral infarct.Semantic proximity Read ↗

Common mutations at the homocysteine metabolism pathway and pediatric stroke.Semantic proximity Read ↗

EPCR gene A3 haplotype and elevated soluble endothelial protein C receptor (sEPCR) levels in Turkish pediatric stroke patients.Semantic proximity Read ↗

Prothrombotic gene polymorphisms and atherothrombotic cerebral infarction.Semantic proximity Read ↗

Clinical significance of factor V Leiden and prothrombin G20210A-mutations in cerebral venous thrombosis - comparison with arterial ischemic stroke.Semantic proximity Read ↗

Prothrombin gene G20210-->A transition is a risk factor for cerebral venous thrombosis.Semantic proximity Read ↗

Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patients.Semantic proximity Read ↗

Genetic risk factors of thrombophilia in ischaemic childhood stroke of cardiac origin. A prospective ESPED survey.Semantic proximity Read ↗

Search for genetic factors favoring thrombosis in Turkish population.Semantic proximity Read ↗

Significance of factor V, prothrombin, MTHFR, and PAI-1 genotypes in childhood cerebral thrombosis.Semantic proximity Read ↗

Genetic risk factors in young adults with 'cryptogenic' ischemic cerebrovascular disease.Semantic proximity Read ↗

Prothrombin gene variant (G20210A) in a patient with cerebral venous sinus thrombosis.Semantic proximity Read ↗

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