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

von Willebrand disease in China.

Chinese medical journal - 1 Aug 2000

Wang Y, Li Z, Gu J, Ruan C

Abstract excerpt

PURPOSE: To review the molecular pathogenesis in Chinese patients with von Willebrand disease (vWD) and polymorphisms of von Willebrand factor (vWF) in Chinese population. DATA SOURCES: Both Chinese and English language literature search using MEDLINE (1985-1998), and original articles published in main Chinese and international journals. STUDY SELECTION AND DATA EXTRACTION: After reviewing of the literature, 19...

Read the complete abstract on PubMed

Topics

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

Share to Mutation
Share to Point Mutation
Share to Polymorphism, Genetic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to von Willebrand Diseases

Source

Identifiers

PMID: 11776047

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

von Willebrand disease in China.PMID 11776047Read ↗

Molecular diagosis of von Willebrand disease.Semantic proximity Read ↗

Diagnosis and management of von Willebrand disease in China.Semantic proximity Read ↗

[The phenotypic and genotypic diagnosis of three Chinese patients with von Willebrand disease].Semantic proximity Read ↗

Von Willebrand disease mutation spectrum and associated mutation mechanisms.Semantic proximity Read ↗

Molecular and clinical profile of VWD in a large cohort of Chinese population: application of next generation sequencing and CNVplex® technique.Semantic proximity Read ↗

[Phenotype and genotype analysis of three Chinese pedigrees with von Willebrand disease].Semantic proximity Read ↗

A standard nomenclature for von Willebrand factor gene mutations and polymorphisms. On behalf of the ISTH SSC Subcommittee on von Willebrand factor.Semantic proximity Read ↗

Patients with von Willebrand disease in China: Results of an online survey.Semantic proximity Read ↗

[Study on genetic mutations of the vWF in type 2A von Willebrand disease].Semantic proximity Read ↗

[Molecular genetics of von Willebrand disease].Semantic proximity Read ↗

A Compound Heterozygosis of Two Novel Mutations in vWF Exacerbates vWD in a Chinese Pedigree.Semantic proximity Read ↗

Structure and function of von Willebrand factorSemantic proximity Read ↗

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