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

A hereditary angioedema screening on an index case: Turkey.

Asian Pacific journal of allergy and immunology - 1 Sept 2019

Ozkars Mehmet Yasar, Keskin Ozlem, Bayram Nazan, Keskin Mehmet, Bayram Hasan, Sahin Yavuz, Kucukosmanoglu Ercan, Attila Nurhan, Kirik Serkan Kirik

Abstract excerpt

BACKGROUND: Hereditary angioedema (HAE) is characterised by recurrent episodes of angioedema and can be fatal. OBJECTIVE: The present study aimed to screen HAE. METHODS: A total of 60 individuals were screened. The frequency and severity of symptoms were scored from 0 to 8. Measurements were taken of C4 and C1 esterase inhibitor protein (C1-INH) levels. Mutation in the C1 inhibitor gene was examined in 9 patients...

Read the complete abstract on PubMed

Topics

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

Share to Angioedemas, Hereditary
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Complement C1 Inhibitor Protein

Share to Complement C4

Share to DNA Mutational Analysis

Share to Genetic Testing

Share to Infant

Share to Pedigree

Source

Identifiers

PMID: 30118244
DOI: 10.12932/AP-060218-0257

Genes

SERPING1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A hereditary angioedema screening on an index case: Turkey.PMID 30118244Read ↗

Hereditary AngioedemaSemantic proximity Read ↗

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

Frequent life-threatening laryngeal attacks in two Croatian families with hereditary angioedema due to C1 inhibitor deficiency harbouring a novel frameshift mutation in SERPING1.Semantic proximity Read ↗

Genetic Study of Hereditary Angioedema Type I and Type II (First Report from Iranian Patients: Describing Three New Mutations).Semantic proximity Read ↗

The Burden of Hereditary Angioedema in a Large Family in Brazil.Semantic proximity Read ↗

Hereditary Angioedema Due to C1 Inhibitor Deficiency in Serbia: Two Novel Mutations and Evidence of Genotype-Phenotype AssociationSemantic proximity Read ↗

Case Report: Early presentation of hereditary angioedema symptoms in a 2-year-old boySemantic proximity Read ↗

Clinical manifestations of hereditary angioedema: a systematic review of treatmentSemantic proximity Read ↗

Type II hereditary angioedema with an apparently de novo SERPING1 mutation in China: A case report and family screening.Semantic proximity Read ↗

Hereditary and acquired angioedema: problems and progress: proceedings of the third C1 esterase inhibitor deficiency workshop and beyond.Semantic proximity Read ↗

The Turkish Hereditary Angioedema Pilot Study (TURHAPS): the first Turkish series of hereditary angioedema.Semantic proximity Read ↗

Hereditary and acquired angioedema.Semantic proximity Read ↗

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