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

Hereditary angioedema with normal C1-INH with versus without specific F12 gene mutations.

Allergy - 1 Aug 2015

Bork K, Wulff K, Witzke G, Hardt J

Abstract excerpt

BACKGROUND: Hereditary angioedema with normal C1-INH may be linked to specific mutations in the coagulation factor 12 (FXII) gene (HAE-FXII) or mutations in genes that are still unknown (HAE-unknown). To assess the differences in transmission and inheritance, clinical features, and laboratory parameters between patients with HAE-FXII and HAE-unknown. METHODS: Sixty-nine patients with HAE-FXII from 23 unrelated...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Age Distribution
Share to Angioedemas, Hereditary
Share to Complement C1 Inhibitor Protein

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Databases, Factual

Share to Factor XII

Share to Incidence

Share to Severity of Illness Index

Share to Sex Distribution

Source

Identifiers

PMID: 25952149
DOI: 10.1111/all.12648

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hereditary angioedema with normal C1-INH with versus without specific F12 gene mutations.PMID 25952149Read ↗

Hereditary Angioedema with Normal C1 Inhibitor and F12 Mutations in 42 Brazilian Families.Semantic proximity Read ↗

Coagulation Factor XII Gene Mutation in Brazilian Families with Hereditary Angioedema with Normal C1 Inhibitor.Semantic proximity Read ↗

Characterization of patients with angioedema without wheals: the importance of F12 gene screening.Semantic proximity Read ↗

Hereditary angioedema: Pathophysiology (HAE type I, HAE type II, and HAE nC1-INH).Semantic proximity Read ↗

Hereditary and acquired angioedema.Semantic proximity Read ↗

Hereditary angioedema with normal C1 inhibitor and factor XII mutation: a series of 57 patients from the French National Center of Reference for Angioedema.Semantic proximity Read ↗

Hereditary angioedema with normal C1-inhibitor: Clinical and genetic characterization of 15 Portuguese unrelated families.Semantic proximity Read ↗

Hereditary Angioedema with Normal C1 Inhibitor: Update on Evaluation and Treatment.Semantic proximity Read ↗

Clinical features of genetically characterized types of hereditary angioedema with normal C1 inhibitor: a systematic review of qualitative evidence.Semantic proximity Read ↗

SERPING1 Variants and C1-INH Biological Function: A Close Relationship With C1-INH-HAESemantic proximity Read ↗

Incidental findings related to genes associated to HAE-nC1INH: how to proceed?Semantic proximity Read ↗

Hereditary angioedema with F12 mutation: factors modifying the clinical phenotype.Semantic proximity Read ↗

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