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

Combined thrombophilic mutations in women with unexplained recurrent miscarriage.

American journal of reproductive immunology (New York, N.Y. : 1989) - 1 Feb 2007

Sotiriadis Alexandros, Vartholomatos George, Pavlou Matthaios, Kolaitis Nicolaos, Dova Leucothea, Stefos Theodor, Paraskevaidis Evangelos, Kalantaridou Sophia N

Abstract excerpt

PROBLEM: To compare the prevalence of five common thrombophilic polymorphisms and their combination in women with recurrent miscarriage and a control group. METHOD OF STUDY: Genomic analysis using polymerase chain reaction (PCR) was carried out in patients with two or more miscarriages and contro...

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 Polymerase Chain Reaction

Share to Pregnancy

Share to Prothrombin

Share to Thrombophilia

Source

Identifiers

PMID: 17217367
DOI: 10.1111/j.1600-0897.2006.00454.x

Genes

MTHFR

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17217367-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Combined thrombophilic mutations in women with unexplained recurrent miscarriage.PMID 17217367Read ↗

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

Genetic thrombophilic mutations among couples with recurrent miscarriage.Semantic proximity Read ↗

Fibrinolytic Defects and Recurrent MiscarriageSemantic 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 ↗

Testing for Inherited Thrombophilia in Recurrent MiscarriageSemantic proximity Read ↗

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

Maternal factor V Leiden and prothrombin mutations do not seem to contribute to the occurrence of two or more than two consecutive miscarriages in Caucasian patients.Semantic proximity Read ↗

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

Recurrent miscarriage and thrombophiliaSemantic proximity Read ↗

Effects of inherited thrombophilia in women with recurrent pregnancy loss.Semantic proximity Read ↗

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

Genetics of Recurrent Miscarriage: Challenges, Current Knowledge, Future DirectionsSemantic proximity Read ↗

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