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

Budd-Chiari syndrome in a patient heterozygous for the G20210A mutation of the prothrombin gene.

Thrombosis and haemostasis - 1 Feb 1998

Bucciarelli P, Franchi F, Alatri A, Bettini P, Moia M

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 Budd-Chiari Syndrome
Share to Heterozygote
Share to Liver Transplantation
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Prothrombin

Source

Identifiers

PMID: 9493607

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Budd-Chiari syndrome in a patient heterozygous for the G20210A mutation of the prothrombin gene.PMID 9493607Read ↗

Budd-Chiari syndrome in a patient heterozygous for both factor V Leiden and the G20210A mutation on the prothrombin gene.Semantic proximity Read ↗

Compound heterozygosity for factor V Leiden and prothrombin G20210A mutations in a child with Budd-Chiari syndrome.Semantic proximity Read ↗

Prothrombin gene mutation in Budd-Chiari syndrome-The first case report from India.Semantic proximity Read ↗

Chronic thromboembolic pulmonary hypertension in a patient heterozygous for both factor V Leiden and G20210 prothrombin mutation.Semantic proximity Read ↗

Homozygous G20210A transition in the prothrombin gene associated with severe venous thrombotic disease: two cases in a French family.Semantic proximity Read ↗

Eclampsia in a woman homozygous for the prothrombin G20210A mutation.Semantic proximity Read ↗

[Budd-Chiari Syndrome in a patient with essential thrombocytopenia carrier of the prothrombin gene mutation G2021A].Semantic proximity Read ↗

Sweet's syndrome in a woman with a prothrombin gene (G20210A) mutation.Semantic proximity Read ↗

Heterozygous prothrombin G20210A gene mutation in a patient with livedoid vasculitis.Semantic proximity Read ↗

Homozygous G20210A prothrombin gene mutation without thromboembolic events: a case report.Semantic proximity Read ↗

Homozygous factor V Leiden mutation in a child with Budd-Chiari syndrome.Semantic proximity Read ↗

Double-homozygosity for factor V Leiden and the prothrombin gene G20210A variant in a young patient with idiopathic venous thrombosis.Semantic proximity Read ↗

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