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

Effects of inherited thrombophilia in women with recurrent pregnancy loss.

Clinical and experimental obstetrics & gynecology - 1 Jan 2011

Habibovic Z, Zeybek B, Sanhal C, Eroglu Z, Karaca E, Ulukus M

Abstract excerpt

PURPOSE OF INVESTIGATION: To evaluate the prevalence and effects of inherited thrombophilia caused by factor V Leiden, prothrombin G20210A and methylenetetrahydrofolate reductase (MTHFR) C677T mutations in women with recurrent pregnancy loss. METHODS: A study group of 97 women with recurrent miscarriages and a control group of 71 healthy pregnant women were included in the study. Genotype analyses for factor V...

Read the complete abstract on PubMed

Topics

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

Share to Abortion, Habitual
Share to Case-Control Studies
Share to Factor V

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Methylenetetrahydrofolate Reductase (NADPH2)

Share to Pregnancy

Share to Prothrombin

Share to Thrombophilia

Share to Young Adult

Source

Identifiers

PMID: 22268272

Genes

MTHFR

Variants

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

Effects of inherited thrombophilia in women with recurrent pregnancy loss.PMID 22268272Read ↗

Prevalence of genetic markers for thrombophilia in recurrent pregnancy loss.Semantic proximity Read ↗

Factor V Leiden and prothrombin G20210A mutations, but not methylenetetrahydrofolate reductase C677T, are associated with recurrent miscarriagesSemantic proximity Read ↗

Inherited thrombophilia with recurrent pregnancy loss in Turkish women--a real phenomenon?Semantic proximity Read ↗

Thrombophilias and recurrent pregnancy loss: a critical appraisal of the literature.Semantic proximity Read ↗

Which thrombophilic gene mutations are risk factors for recurrent pregnancy loss?Semantic proximity Read ↗

[Genetic thrombophilic defects (Factor V Leiden, prothrombin G20210A, MTHFR C677T) in women with recurrent fetal loss].Semantic proximity Read ↗

The association between inherited thrombophilia and recurrent pregnancy loss in Turkish women.Semantic proximity Read ↗

G20210A prothrombin gene mutation: prevalence in a recurrent miscarriage population.Semantic proximity Read ↗

A Pilot Study on Multigenic Thrombophilic Risk in Recurrent Pregnancy Loss: Interactions Between MTHFR Polymorphisms and Classical Thrombophilia-Associated SNPs.Semantic proximity Read ↗

Etiology of hypercoagulable state in women with recurrent fetal loss without other causes of miscarriage from Southern Italy: new clinical target for antithrombotic therapySemantic proximity Read ↗

Multiple thrombophilic gene mutations rather than specific gene mutations are risk factors for recurrent miscarriage.Semantic proximity Read ↗

Evaluation of the association between hereditary thrombophilias and recurrent pregnancy loss: a meta-analysis.Semantic proximity Read ↗

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