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 with underlying homozygous factor V Leiden and heterozygous methylenetetrahydrofolate reductase mutations.

Journal of gastroenterology - 1 Oct 2005

Barada Kassem A, Azar Cecilio R, Otrock Zaher K, Taher Ali T

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 Factor V
Share to Heterozygote
Share to Homozygote

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Methylenetetrahydrofolate Reductase (NADPH2)

Share to Mutation

Share to Point Mutation

Source

Identifiers

PMID: 16261441
DOI: 10.1007/s00535-005-1664-2

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Budd-Chiari syndrome with underlying homozygous factor V Leiden and heterozygous methylenetetrahydrofolate reductase mutations.PMID 16261441Read ↗

Budd-Chiari syndrome and factor V Leiden mutation.Semantic proximity Read ↗

Budd-Chiari syndrome and factor V Leiden mutation.Semantic proximity Read ↗

Compound heterozygosity for factor V and methylenetetrahydrofolate reductase mutations in a patient with Budd-Chiari syndrome.Semantic proximity Read ↗

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

Budd-Chiari syndrome in a paroxysmal nocturnal hemoglobinuria patient with coexistence of factor II and MTHFR mutations.Semantic proximity Read ↗

[Budd-chiari syndrome and heterozygotic mutation of metylenetetrahidrofolate reductase].Semantic proximity Read ↗

Inherited factor VII deficiency: molecular genetics and pathophysiology.Semantic proximity Read ↗

Budd-Chiari syndrome: combination of genetic defects and the use of oral contraceptives leading to hypercoagulability.Semantic proximity Read ↗

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

Inherited factor X deficiency: molecular genetics and pathophysiology.Semantic proximity Read ↗

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

Homocystinuria (methylenetetrahydrofolate reductase deficiency) and mutation of factor V gene.Semantic proximity Read ↗

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