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

Laboratory tests for precise classification and genetic analysis of von Willebrand disease.

Sbornik lekarsky - 1 Jan 2003

Habart D, Vorlová Z

Abstract excerpt

von Willebrand disease (vWD) is the most common inherited bleeding disorder, which is highly heterogeneous ranging from asymptomatic laboratory abnormality to a life threatening bleeding. The condition is caused by a quantitative or qualitative deficiency of von Willebrand factor (vWF). Since 199...

Read the complete abstract on PubMed

Topics

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

Share to Mutation
Share to Polymorphism, Genetic
Share to von Willebrand Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to von Willebrand Factor

Source

Identifiers

PMID: 14577134

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-14577134-2026-09-02.1. Manifest publication-graph-cohort-2026-09-02.1.

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

Laboratory tests for precise classification and genetic analysis of von Willebrand disease.PMID 14577134Read ↗

Laboratory diagnosis and molecular classification of von Willebrand disease.Semantic proximity Read ↗

Phenotypic and genotypic diagnosis of von Willebrand disease: a 2004 update.Semantic proximity Read ↗

Developments in the diagnostic procedures for von Willebrand disease.Semantic proximity Read ↗

The molecular analysis of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organisation Haemophilia Genetics Laboratory Network.Semantic proximity Read ↗

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

von Willebrand disease update: diagnostic and treatment dilemmas.Semantic proximity Read ↗

Diagnosis of von Willebrand disease subtypes: implications for treatment.Semantic proximity Read ↗

Analysis of von Willebrand Disease in the “Heart of Europe”Semantic proximity Read ↗

von Willebrand disease: Diagnosis and treatment, treatment of women, and genomic approach to diagnosis.Semantic proximity Read ↗

Application of genetic testing for the diagnosis of von Willebrand disease.Semantic proximity Read ↗

New developments in von Willebrand disease.Semantic proximity Read ↗

[Biological diagnosis of Von Willebrand disease and its difficulties].Semantic proximity Read ↗

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