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Pathology|April 23, 1999
A comparison of commercial and in-house ELISAs for antineutrophil cytoplasmic antibodies directed against proteinase 3 and myeloperoxidaseW Pollock, K Dunster, J M Rolland, et al.
Kidney International|March 18, 2000
Antineutrophil cytoplasmic antibodies and associated diseases: a review of the clinical and laboratory featuresJ Savige, D Davies, R J Falk, et al.
Clinical and Experimental Rheumatology|January 2, 2003
Antineutrophil cytoplasmic antibody (ANCA)-associated systemic vasculitis after immunisation with bacterial proteinsJ Savige, L Nassis, T Cooper, et al.
Ophthalmic Genetics|January 3, 2001
Absence of ocular manifestations in autosomal dominant Alport syndrome associated with haematological abnormaltiesD Colville, Y Y Wang, R Jamieson, et al.
Ophthalmic Genetics|November 15, 1997
Ocular manifestations of autosomal recessive Alport syndromeD Colville, J Savige, M Morfis, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 6, 1998
Anti-glomerular basement membrane (GBM)-antibody-mediated disease with normal renal functionC Ang, J Savige, J Dawborn, et al.
Clinical Nephrology|March 1, 1997
Classical polyarteritis nodosa and microscopic polyarteritis with medium vessel involvement--a comparison of the clinical and laboratory featuresG S Kirkland, J Savige, D Wilson, et al.
The British Journal of Ophthalmology|November 21, 2008
The dot-and-fleck retinopathy of X linked Alport syndrome is independent of complement factor H (CFH) gene polymorphismsJ Liu, D Colville, Y Y Wang, et al.
Kidney International|March 1, 1995
Bull terrier hereditary nephritis: a model for autosomal dominant Alport syndromeJ C Hood, J Savige, A Hendtlass, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 1, 2001
A comparison of the clinical, histopathologic, and ultrastructural phenotypes in carriers of X-linked and autosomal recessive Alport's syndromeH Dagher, M Buzza, D Colville, et al.
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