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

Frequency of complement third component (C3) and properdin factor (BF) phenotypes in patients with various clinical manifestations of HBV infection.

European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics - 1 Feb 1996

Kacprzak-Bergman I, Halasa J

Abstract excerpt

Four groups of children were tested for the distribution of C3 and BF phenotypes: HBV-infected patients with Gianotti-Crosti syndrome, with CAH and with glomerulonephritis, and healthy children. The frequency of the phenotype C3F was significantly higher in children with Gianotti-Crosti syndrome in comparison with healthy children. The frequency of the phenotype BFS was significantly higher in patients with...

Read the complete abstract on PubMed

Topics

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

Share to Child
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Complement C3

Share to Hepatitis B

Share to Hepatitis, Chronic

Share to Phenotype

Source

Identifiers

PMID: 8834917
DOI: 10.1111/j.1744-313x.1996.tb00258.x

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Frequency of complement third component (C3) and properdin factor (BF) phenotypes in patients with various clinical manifestations of HBV infection.PMID 8834917Read ↗

Phenotype distribution of the third component of complement (C3) and of the properdin B factor (BF) in children with mumps meningitis.Semantic proximity Read ↗

Polymorphism of the fourth component of complement (C4) and three clinical pictures of hepatitis B virus infection in children.Semantic proximity Read ↗

Relationship between genotypes and clinical manifestation, pathology, and cccDNA in Chinese children with hepatitis B virus-associated glomerulonephritis.Semantic proximity Read ↗

The genotype C could play a key role in hepatitis B virus associated nephritis among the northwest Chinese children.Semantic proximity Read ↗

C4, BF, C3 allele distribution and complement activity in healthy aged people and centenarians.Semantic proximity Read ↗

Complement factor B allotypes in the susceptibility and severity of coeliac disease in patients and relatives.Semantic proximity Read ↗

[Clinical and pathological differences between children with various genotypes of hepatitis B virus-associated glomerulonephritis].Semantic proximity Read ↗

[Genetic polymorphism of properdin factor B in the Han population in Chengdu, China].Semantic proximity Read ↗

DBP (vitamin D binding protein) and BF (properdin factor B) allele distribution in Namibian San and Khoi and in other South African populations.Semantic proximity Read ↗

Hereditary subtypic patterns detected in the Ba fragment of complement factor B: occurrence of four common alleles in Japanese.Semantic proximity Read ↗

Complement C3 F and BF S allotypes are risk factors for Chagas disease cardiomyopathy.Semantic proximity Read ↗

Serum complement (C3, BF, C4) types in Swedish Saamis.Semantic proximity Read ↗

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