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

Congenital factor V deficiency and decreased VWF in a Chinese male patient with hematuria.

Haemophilia : the official journal of the World Federation of Hemophilia - 1 Jan 2018

Wang X, Tang N, Lu Y, Li D

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 Factor V Deficiency
Share to VWF gene
Share to Hematuria
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Pedigree

Share to von Willebrand Factor

Source

Identifiers

PMID: 29105952
DOI: 10.1111/hae.13363

Genes

VWF

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Congenital factor V deficiency and decreased VWF in a Chinese male patient with hematuria.PMID 29105952Read ↗

Inherited factor VII deficiency: molecular genetics and pathophysiology.Semantic proximity Read ↗

Inherited resistance to activated protein C, a major basis of venous thrombosis, is caused by deficient anticoagulant cofactor function of factor V.Semantic proximity Read ↗

Clinical Characterization and Molecular Analysis of Fourteen Chinese Patients with Factor V Deficiency.Semantic proximity Read ↗

Protein C and Protein S Deficiencies Are the Most Important Risk Factors Associated with Thrombosis in Chinese Venous Thrombophilic Patients in TaiwanSemantic proximity Read ↗

Similarity in joint and mucous bleeding syndromes in type 2N von Willebrand disease and severe hemophilia A coexisting with type 1 von Willebrand disease in two Chinese pedigrees.Semantic proximity Read ↗

Inherited factor V deficiency associated with a novel heterozygous missense mutation (p.G493R) in a patient with excessive surgical bleeding.Semantic proximity Read ↗

First molecular characterization of a patient with combined factor V and factor VII deficiency.Semantic proximity Read ↗

[A novel mutation causes congenital factor V deficiency].Semantic proximity Read ↗

Japanese family with congenital factor VII deficiency.Semantic proximity Read ↗

Factor V mutations in Iranian patients with activated protein C resistance and venous thrombosis.Semantic proximity Read ↗

Pathogenetic role of Factor VII deficiency and thrombosis in cross-reactive material positive patients.Semantic proximity Read ↗

[Two novel factor V gene mutations associated with congenital coagulation factor V deficiency, study of one pedigree].Semantic proximity Read ↗

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