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Article

Increased frequency of C4B*Q0 alleles in patients with Henoch-Schönlein purpura.

Scandinavian journal of immunology - 1 Mar 2005

Stefansson Thors V, Kolka R, Sigurdardottir S L, Edvardsson V O, Arason G, Haraldsson A

Abstract excerpt

Henoch-Schonlein purpura (HSP) is a vasculitis of unknown aetiology, possibly involving immune complexes. The complement system is essential for the clearance of immune complexes. Our aim was to explore the hypothesis that patients with HSP have abnormal complements, contributing to the development of the disease. The study included 56 patients diagnosed with HSP at the Children's Hospital, Iceland between 1984...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 15787745
DOI: 10.1111/j.1365-3083.2005.01533.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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