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

HELLP syndrome with fetal growth retardation in a woman homozygous for the prothrombin gene variant 20210A.

Thrombosis and haemostasis - 1 Apr 2005

Moessmer Georg, Müller Burkhardt, Kolben Martin, Schmitt Manfred, Schneider Karl Theodor Maria, Artmann Almut

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Fetal Growth Retardation
Share to Homozygote
Share to Polymorphism, Single Nucleotide
Share to Pre-Eclampsia

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Pregnancy

Share to Prothrombin

Share to Thrombophilia

Source

Identifiers

PMID: 15841328

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

HELLP syndrome with fetal growth retardation in a woman homozygous for the prothrombin gene variant 20210A.PMID 15841328Read ↗

A homozygosity state for 20210A prothrombin variant in a young woman as cause of a deep venous thrombosis during pregnancy.Semantic proximity Read ↗

Prothrombin gene variants in non-Caucasians with fetal loss and intrauterine growth retardation.Semantic proximity Read ↗

Partial HELLP syndrome (ELLP) in a woman heterozygous for the prothrombin G20210A mutation.Semantic proximity Read ↗

Eclampsia in a woman homozygous for the prothrombin G20210A mutation.Semantic proximity Read ↗

A three-generation family presenting five cases of homozygosity for the 20210 G to A prothrombin variant.Semantic proximity Read ↗

Pregnancy Complications In G20210A Mutation Carriers Associated With High Prothrombin ActivitySemantic proximity Read ↗

Budd-Chiari syndrome in a patient heterozygous for the G20210A mutation of the prothrombin gene.Semantic proximity Read ↗

Superior sagittal sinus thrombosis in a patient heterozygous for the novel 20210 A allele of the prothrombin gene.Semantic proximity Read ↗

Maternal and fetal thrombophilia in intrauterine growth restriction in the presence or absence of maternal hypertensive disease.Semantic proximity Read ↗

Cardiology patient pages. Prothrombin 20210 mutation (factor II mutation).Semantic proximity Read ↗

"20209C-T" a variant mutation of prothrombin gene mutation in a patient with recurrent pregnancy loss.Semantic proximity Read ↗

Budd-Chiari syndrome in a patient heterozygous for both factor V Leiden and the G20210A mutation on the prothrombin gene.Semantic proximity Read ↗

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