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

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

Revista clinica espanola - 1 Oct 2008

Campos Franco J, Otero Antón E, López Rodríguez R, Mallo González N, Pérez Pampín E, Alende Sixto R

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 Mutation
Share to Prothrombin

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Thrombocythemia, Essential

Source

Identifiers

PMID: 19000481
DOI: 10.1157/13127615

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 with essential thrombocytopenia carrier of the prothrombin gene mutation G2021A].PMID 19000481Read ↗

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

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

[Massive pulmonary embolism in a patient with an unusual combination of prothrombotic genetic factors].Semantic proximity Read ↗

[Analysis of clinical features and genotype in an inherited coagulation factor Ⅶ deficiency pedigree].Semantic proximity Read ↗

[HELLP syndrome associated to pulmonary thromboembolism and factor V Leiden].Semantic proximity Read ↗

[Thrombophilia--often a case of genetic susceptibility. Thrombosis ABC, 6: Protein C deficiency].Semantic proximity Read ↗

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

[Portal and mesenteric vein thrombosis in a patient with a mutation of the 20210 gen of the prothrombin].Semantic proximity Read ↗

[Analysis of the molecular pathogenesis and clinical phenotypes of 10 patients with inherited coagulation factor Ⅺ deficiency].Semantic proximity Read ↗

[Phenotypic and genetic analysis of a pedigree with inherited antithrombin deficiency].Semantic proximity Read ↗

Arterial and venous thrombosis and prothrombotic fibrin clot phenotype in a Polish family with type 1 antithrombin deficiency (antithrombin Krakow).Semantic proximity Read ↗

[Clinical and genetic analysis of pulmonary embolism induced by a novel gene mutation of the antithrombin Ⅲ gene].Semantic proximity Read ↗

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