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

Clinical characteristics, genes identification and follow-up study of a patient with central venous thrombosis from a protein S deficiency pedigree.

European review for medical and pharmacological sciences - 1 Jan 2021

Wang T, Zhao X-J, Zhu H-D, Lu M, Wen B, Ma L

Abstract excerpt

OBJECTIVE: To explore the clinical and prognostic features of CVT caused by PROS1 gene mutations and to provide clinical experience for new oral anticoagulants, such as rivaroxaban, in the treatment of CVT with a high risk of thrombosis. PATIENTS AND METHODS: The CVT patient's clinical symptoms were described, and the brain imaging and blood coagulation tests were performed to confirm the diagnosis of CVT. The...

Read the complete abstract on PubMed

Topics

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

Share to Administration, Oral
Share to Anticoagulants

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Blood Coagulation

Share to Follow-Up Studies

Share to Protein S

Share to Protein S Deficiency

Share to Thrombophilia

Share to Venous Thrombosis

Source

Identifiers

PMID: 33506924
DOI: 10.26355/eurrev_202101_24402

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical characteristics, genes identification and follow-up study of a patient with central venous thrombosis from a protein S deficiency pedigree.PMID 33506924Read ↗

Clinical Manifestation and Mutation Spectrum of 53 Unrelated Pedigrees with Protein S Deficiency in ChinaSemantic proximity Read ↗

Lessons from an elderly patient with pulmonary embolism caused by protein S deficiency: a case report.Semantic proximity Read ↗

A new hereditary PROS1 gene mutation caused isolated cortical venous thrombosis.Semantic proximity Read ↗

A Thrombophilia Family With Protein S Deficiency Due to Protein Translation Disorders Caused By a Leu607Ser Heterozygous Mutation in PROS1Semantic proximity Read ↗

Venous thromboembolism associated with protein S deficiency due to Arg451* mutation in PROS1 gene: a case report and a literature review.Semantic proximity Read ↗

Molecular basis of protein S deficiency in ChinaSemantic proximity Read ↗

An interactive human PROS1 variants database provides novel insights into the genetics and phenotypes of inherited protein S deficiency.Semantic proximity Read ↗

Recurrent pulmonary embolism associated with deep venous thrombosis diagnosed as protein s deficiency owing to a novel mutation in PROS1: A case report.Semantic proximity Read ↗

PROS1 genotype phenotype relationships in a large cohort of adults with suspicion of inherited quantitative protein S deficiency.Semantic proximity Read ↗

A new hereditary PROS1 mutation caused isolated cortical venous thrombosis: a case report and literature reviewSemantic proximity Read ↗

PROS1 mutations associated with protein S deficiency in Polish patients with residual vein obstruction on rivaroxaban therapy.Semantic proximity Read ↗

Genetic analysis, phenotypic diagnosis, and risk of venous thrombosis in families with inherited deficiencies of protein S.Semantic proximity Read ↗

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