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

Inherited thrombophilias and pre-eclampsia in Brazilian women.

European journal of obstetrics, gynecology, and reproductive biology - 1 Sept 2007

Dusse Luci Maria Santana, Carvalho Maria das Graças, Bragança William Fialho, Paiva Sabrina Guimarães, Godoi Lara Carvalho, Guimarães Daniela Amorim Melgaço, Fernandes Ana Paula

Abstract excerpt

OBJECTIVE: The aim of the present study was to compare the distribution of G1691A, G20210A and C677T mutations in pre-eclamptic Brazilian women and in matched control women with an uncomplicated normal pregnancy. STUDY DESIGN: these mutations were investigated by PCR-RFLP in 83 normal pregnancies (control group) and in 30 pre-eclamptic pregnant women (severe form). RESULTS: G1691A mutation was detected neither in...

Read the complete abstract on PubMed

Topics

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

Share to Brazil
Share to Case-Control Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Factor V

Share to Methylenetetrahydrofolate Reductase (NADPH2)

Share to Pre-Eclampsia

Share to Pregnancy

Share to Prothrombin

Share to Thrombophilia

Source

Identifiers

PMID: 17097210
DOI: 10.1016/j.ejogrb.2006.09.006

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Inherited thrombophilias and pre-eclampsia in Brazilian women.PMID 17097210Read ↗

Analysis of factor V Leiden and prothrombin mutations in patients with suspected thrombophilia in São Paulo state-BrazilSemantic proximity Read ↗

Thrombophilic mutations and susceptibility to preeclampsia in Western Iran.Semantic proximity Read ↗

Factor-V Leiden G1691A and prothrombin G20210A polymorphisms in Sudanese women with preeclampsia, a case -control studySemantic proximity Read ↗

Increased frequency of genetic thrombophilia in women with complications of pregnancy.Semantic proximity Read ↗

Acquired activated protein C resistance, thrombophilia and adverse pregnancy outcomes: a study performed in an Irish cohort of pregnant women.Semantic proximity Read ↗

Prevalence of prothrombotic polymorphisms in Greece.Semantic proximity Read ↗

The significance of genetic polymorphisms of factor V Leiden and prothrombin in the preeclamptic Polish women.Semantic proximity Read ↗

Genetics of suspected thrombophilia in Serbian females with infertility, including three cases, homozygous for FII 20210A or FV 1691A mutations.Semantic proximity Read ↗

[Genetic mutations, acquired coagulation system disorders and obstetric pathology. Personal experience].Semantic proximity Read ↗

[The role of 1691G>A (Leiden) mutation in Factor V gene, 20210G>A in prothrombin gene and 677C>T in MTHFR gene in etiology of early pregnancy loss].Semantic proximity Read ↗

Prevalence of antiphospholipid antibodies, factor V G1691A (Leiden) and prothrombin G20210A mutations in early and late recurrent pregnancy loss.Semantic proximity Read ↗

Prevalence of F5 1691G>A, F2 20210G>A, and MTHFR 677C>T polymorphisms in Bosnian women with pregnancy loss.Semantic proximity Read ↗

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