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

Distribution of von Willebrand factor levels in young women with and without bleeding symptoms: influence of ABO blood group and promoter haplotypes.

Thrombosis and haemostasis - 1 Jun 2008

Lethagen Stefan, Hillarp Andreas, Ekholm Caroline, Mattson Eva, Halldén Christer, Friberg Britt

Abstract excerpt

The normal distribution of von Willebrand factor (VWF) levels is wide. Low levels are associated with bleeding symptoms and von Willebrand disease (VWD). We have recently described a high prevalence of bleeding symptoms in a whole age group of young females (n = 1,019) from Malmo, Sweden. It was...

Read the complete abstract on PubMed

Topics

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

Share to ABO Blood-Group System
Share to Hemorrhage
Share to Prevalence

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Promoter Regions, Genetic

Share to Surveys and Questionnaires

Share to Sweden

Share to von Willebrand Diseases

Share to von Willebrand Factor

Source

Identifiers

PMID: 18521502
DOI: 10.1160/TH07-06-0419

Genes

VWF
ABO

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18521502-2026-09-02.2. 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

Distribution of von Willebrand factor levels in young women with and without bleeding symptoms: influence of ABO blood group and promoter haplotypes.PMID 18521502Read ↗

Von Willebrand disease: classification and epidemiology.Semantic proximity Read ↗

Genetic study of von Willebrand factor antigen levels ≤ 50 IU/dL identifies variants associated with increased risk of von Willebrand disease and bleeding.Semantic proximity Read ↗

Unraveling the Influence of Common von Willebrand factor variants on von Willebrand Disease Phenotype: An Exploratory Study on the Molecular and Clinical Profile of von Willebrand Disease in Spain Cohort.Semantic proximity Read ↗

Determinants of bleeding phenotype in adult patients with moderate or severe von Willebrand disease.Semantic proximity Read ↗

Mutation distribution in the von Willebrand factor gene related to the different von Willebrand disease (VWD) types in a cohort of VWD patients.Semantic proximity Read ↗

Diagnosis of inherited von Willebrand disease: a clinical perspective.Semantic proximity Read ↗

Genome-wide association studies identify genetic loci for low von Willebrand factor levels.Semantic proximity Read ↗

Plasma levels of plasminogen activator inhibitor-1 and bleeding phenotype in patients with von Willebrand disease.Semantic proximity Read ↗

Variation at the von Willebrand factor (vWF) gene locus is associated with plasma vWF:Ag levels: identification of three novel single nucleotide polymorphisms in the vWF gene promoter.Semantic proximity Read ↗

Phenotypic Parameters in Genotypically Selected Type 2B von Willebrand Disease Patients: A Large, Single-Center Experience Including a New Novel Mutation.Semantic proximity Read ↗

von Willebrand factor variant p.Arg924Gln marks an allele associated with reduced von Willebrand factor and factor VIII levels.Semantic proximity Read ↗

Clinical diagnosis of von Willebrand disease.Semantic proximity Read ↗

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