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

Pathophysiology of Hereditary Angioedema

1 Dec 2014

Abstract excerpt

The genetic deficiency of the C1 inhibitor is responsible for hereditary angioedema (HAE), which is a disease transmitted as an autosomal dominant trait. More than 200 point mutations in the C1 inhibitor gene have been found to be associated with HAE. Patients with this disease suffer from recurrent angioedema, which is mediated by bradykinin derived from activation of the contact system. This system is...

Read the complete abstract on PubMed

Topics

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

Share to Coagulation, Bradykinin, Polyphosphates, and Angioedema
Share to Vitamin K Research Studies

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 25538858
DOI: 10.1089/ped.2014.0425

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

Pathophysiology of Hereditary AngioedemaPMID 25538858Read ↗

Hereditary angioedema.Semantic proximity Read ↗

Hereditary Angioedema: The Clinical Picture of Excessive Contact Activation.Semantic proximity Read ↗

Hereditary and acquired C1-inhibitor-dependent angioedema: from pathophysiology to treatment.Semantic proximity Read ↗

Current update on cellular and molecular mechanisms of hereditary angioedema.Semantic proximity Read ↗

Angioedema attacks in patients with hereditary angioedema: Local manifestations of a systemic activation process.Semantic proximity Read ↗

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

Overview of hereditary angioedema caused by C1-inhibitor deficiency: assessment and clinical management.Semantic proximity Read ↗

Hereditary angioedema: the plasma contact system out of control.Semantic proximity Read ↗

Hereditary Angioedema: Diagnosis, Clinical Implications, and Pathophysiology.Semantic proximity Read ↗

Hereditary and Acquired Angioedema: Heterogeneity of Pathogenesis and Clinical Phenotypes.Semantic proximity Read ↗

Hereditary angioedema: Looking for bradykinin production and triggers of vascular permeabilitySemantic proximity Read ↗

Hereditary and acquired angioedema.Semantic proximity Read ↗

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