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

Adult-onset arterial thrombosis in a pedigree of homozygous and heterozygous protein C deficiency.

Thrombosis research - 1 Jan 2013

Tajima Katsushi, Yamamoto Hisashi, Yamamoto Masakazu, Kato Yuichi, Kato Takeo

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 Age of Onset
Share to Biomarkers
Share to Blood Coagulation
Share to Blood Coagulation Tests

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Heredity

Share to Homozygote

Share to Protein C Deficiency

Share to Thrombosis

Source

Identifiers

PMID: 23174622
DOI: 10.1016/j.thromres.2012.10.016

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

Adult-onset arterial thrombosis in a pedigree of homozygous and heterozygous protein C deficiency.PMID 23174622Read ↗

Novel protein C gene mutation in a compound heterozygote resulting in catastrophic thrombosis in early adulthood: diagnosis and long-term treatment with subcutaneous protein C concentrate.Semantic proximity Read ↗

Inherited defects of the protein C anticoagulant system in childhood thrombo-embolism.Semantic proximity Read ↗

Late onset thrombosis in two Japanese patients with compound heterozygote protein S deficiency.Semantic proximity Read ↗

Protein C deficiency: from gene defects to disease.Semantic proximity Read ↗

Analysis of four hereditary protein C deficiencies associated with vascular thromboembolism.Semantic proximity Read ↗

Protein C deficiency in a family with thromboembolism and identified gene mutations.Semantic proximity Read ↗

Late onset thrombosis in a case of severe protein S deficiency due to compound heterozygosity for PROS1 mutations.Semantic proximity Read ↗

A homozygous protein C deficiency (Lys 192 del) who developed venous thrombosis for the first time at adulthood.Semantic proximity Read ↗

Analysis of Four Hereditary Protein C Deficiencies Associated with Vascular ThromboembolismSemantic proximity Read ↗

Hereditary deficiency of protein C or protein S confers increased risk of arterial thromboembolic events at a young age: results from a large family cohort study.Semantic proximity Read ↗

Asymptomatic Homozygous Protein C DeficiencySemantic proximity Read ↗

Protein S deficiency.Semantic proximity Read ↗

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