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Retinal drusen in glomerulonephritis with or without immune deposits suggest systemic complement act...

Retinal drusen in glomerulonephritis with or without immune deposits suggest systemic complement act...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_a1a3f230d9dd4beaa23d140a7f234b88

Retinal drusen in glomerulonephritis with or without immune deposits suggest systemic complement activation in disease pathogenesis

About this item

Full title

Retinal drusen in glomerulonephritis with or without immune deposits suggest systemic complement activation in disease pathogenesis

Publisher

London: Nature Publishing Group UK

Journal title

Scientific reports, 2022-05, Vol.12 (1), p.8234-8234, Article 8234

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Retinal drusen are characteristic of macular degeneration and complement activation, but also occur in C3, lupus and IgA nephropathy. This cross-sectional observational study compared drusen counts in different forms of glomerulonephritis. Consecutive individuals with glomerulonephritis attending a general renal or transplant clinic underwent retin...

Alternative Titles

Full title

Retinal drusen in glomerulonephritis with or without immune deposits suggest systemic complement activation in disease pathogenesis

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_a1a3f230d9dd4beaa23d140a7f234b88

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_a1a3f230d9dd4beaa23d140a7f234b88

Other Identifiers

ISSN

2045-2322

E-ISSN

2045-2322

DOI

10.1038/s41598-022-12111-w

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