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Scientific Reports|July 11, 2022
Retinal drusen counts are increased in inflammatory bowel disease, and with longer disease duration, more complications and associated IgA glomerulonephritisE Nicklason, Y Ham, D Ng, et al.
Ophthalmic Genetics|February 26, 2016
Retinal disease in the C3 glomerulopathies and the risk of impaired visionJ Savige, L Amos, Frank Ierino, et al.
Kidney International|July 28, 2001
COL4A4 mutation in thin basement membrane disease previously described in Alport syndromeM Buzza, Y Y Wang, H Dagher, et al.
Rheumatology International|June 3, 2000
Clinical associations and characterisation of antineutrophil cytoplasmic antibodies directed against bactericidal/permeability-increasing protein and azurocidinT Cooper, J Savige, L Nassis, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|August 3, 2000
Ultrastructural appearance of renal and other basement membranes in the Bull terrier model of autosomal dominant hereditary nephritisJ C Hood, J Savige, A E Seymour, et al.
Journal of Clinical Pathology|August 27, 2002
Immunofluorescent patterns produced by antineutrophil cytoplasmic antibodies (ANCA) vary depending on neutrophil substrate and conjugateW Pollock, K Clarke, K Gallagher, et al.
Scientific Reports|March 14, 2019
Small vessel disease and intracoronary plaque composition: a single centre cross-sectional observational studyA Wightman, P Barlis, M MacBain, et al.
American Journal of Human Genetics|October 9, 2001
Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromesK E Heath, A Campos-Barros, A Toren, et al.
American Journal of Clinical Pathology|April 7, 1999
International Consensus Statement on Testing and Reporting of Antineutrophil Cytoplasmic Antibodies (ANCA)J Savige, D Gillis, E Benson, et al.
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