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

Recurrent VTE in a heterozygote of the fibrinogen Aα IVS4+1G>T and Aα p.Arg168Ter mutation.

Thrombosis and haemostasis - 2 May 2016

Berens Christina, Rühl Heiko, Ivaškevičius Vytautas, Oldenburg Johannes, Hertfelder Hans-Jörg, Pötzsch Bernd

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 Afibrinogenemia
Share to Anticoagulants
Share to Fibrinogen
Share to Fibrinogens, Abnormal

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hemorrhage

Share to Heterozygote

Share to Recurrence

Share to Venous Thromboembolism

Source

Identifiers

PMID: 26763372
DOI: 10.1160/TH15-10-0818

Variants

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

Recurrent VTE in a heterozygote of the fibrinogen Aα IVS4+1G>T and Aα p.Arg168Ter mutation.PMID 26763372Read ↗

Thrombosis in association with a novel substitution (γ346Gly→Val) at an absolutely conserved site in the fibrinogen γ chain.Semantic proximity Read ↗

Hypodysfibrinogenaemia and thrombosis in association with a new fibrinogen γ chain with two mutations (γ114Tyr→His, and γ320Asp deleted).Semantic proximity Read ↗

Epigenetic, polymorphic and mutational (Αα167Arg→Lys) contribution to a functionally abnormal fibrinogen.Semantic proximity Read ↗

Two different fibrinogen gene mutations associated with bleeding in the same family (A αGly13Glu and γGly16Ser) and their impact on fibrin clot properties: fibrinogen Krakow II and Krakow III.Semantic proximity Read ↗

Congenital Hypodysfibrinogenemia due to γ326Cys→Tyr Mutation: Third Ever-Described Case Associated with Recurrent Venous Thrombosis and COVID Vaccine.Semantic proximity Read ↗

A novel missense mutation in the antithrombin III gene (Ala387-->Val) causing recurrent venous thrombosis.Semantic proximity Read ↗

High risk of thrombosis recurrence in patients with homozygous and compound heterozygous factor V R506Q (Factor V Leiden) and prothrombin G20210ASemantic proximity Read ↗

A Bbeta 14 Arg --> Cys fibrinogen variant in a patient with thrombotic complications (fibrinogen St-Germain III).Semantic proximity Read ↗

A novel missense mutation in the antithrombin III gene (Ser349----Pro) causing recurrent venous thrombosis.Semantic proximity Read ↗

Fibrinogen Otsu I:A gammaAsn319,Asp320 deletion dysfibrinogen identified in an asymptomatic pregnant woman.Semantic proximity Read ↗

Recurrent thromboembolism in two unrelated patients with double heterozygosity for factor V R506Q and factor II 20210G/A mutations.Semantic proximity Read ↗

Hypodysfibrinogenemia causing mild bleeding and thrombotic complications in a compound heterozygote of AalphaIVS4+1G>T mutation and Aalpha4841delC truncation (Aalpha(Perth)).Semantic proximity Read ↗

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