Research Topics
| J SavigeSummaryAffiliation: University of Melbourne Country: Australia Publications
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Detail Information
Publications
Antineutrophil cytoplasmic antibodies and associated diseases: a review of the clinical and laboratory featuresJ Savige
Department of Medicine, University of Melbourne, Austin, Australia
Kidney Int 57:846-62. 2000..Their clinical significance is still largely unclear, and some of the target antigens are present in other cells as well as neutrophils and thus are not strictly "ANCA."..
Thin basement membrane nephropathyJudy Savige
University of Melbourne, Department of Medicine, Austin and Repatriation Medical Centre, Heidelberg, Victoria, Australia
Kidney Int 64:1169-78. 2003..Technical difficulties in the demonstration and interpretation of COL4A3 and COL4A4 mutations mean that mutation detection is not used routinely in the diagnosis of TBMN...
Antineutrophil cytoplasmic antibody (ANCA)-associated systemic vasculitis after immunisation with bacterial proteinsJ Savige
University of Melbourne, Department of Medicine, Austin and Repatriation Medical Centre, Heidelberg, Victoria, Australia
Clin Exp Rheumatol 20:783-9. 2002..The aim of this study was to determine whether the immunisation of rats with bacterial proteins could result in circulating ANCA, T cells with specificity for ANCA antigens, and a systemic vasculitis...
Testing for antineutrophil cytoplasmic antibodiesJ Savige
University Department of Medicine, Austin and Repatriation Medical Centre, Heidelberg, VIC 3084, Australia
Expert Rev Mol Diagn 1:281-9. 2001..International collaborative efforts continue to focus on improving the tests for ANCA...
Segregation of hematuria in thin basement membrane disease with haplotypes at the loci for Alport syndromeM Buzza
Department of Medicine, University of Melbourne, Melbourne, Victoria, Australia
Kidney Int 59:1670-6. 2001..However, nearly half of the families in this study had hematuria that did not segregate with the loci for either autosomal recessive or X-linked Alport syndrome...
COL4A4 mutation in thin basement membrane disease previously described in Alport syndromeM Buzza
University Department of Medicine, Austin and Repatriation Medical Centre, Heidelberg, Victoria, Australia
Kidney Int 60:480-3. 2001..Our observation is evidence that TBMD can represent a carrier state for autosomal-recessive Alport syndrome in at least some individuals...
The binding of proteinase 3 antineutrophil cytoplasmic antibodies (PR3-ANCA) varies in different ELISAsM Trevisin
Immunology Unit, Division of Laboratory Medicine, Austin Hospital, Heidelberg, Victoria 3084, Australia
J Clin Pathol 57:303-8. 2004..This may affect the diagnosis and management of patients with WG, in addition to the implementation of international guidelines for treatment...
A comparison of the clinical, histopathologic, and ultrastructural phenotypes in carriers of X-linked and autosomal recessive Alport's syndromeH Dagher
University Department of Medicine, Ophthalmology Unit, Austin and Repatriation Medical Centre, Heidelberg, Victoria, Australia
Am J Kidney Dis 38:1217-28. 2001..012); however, carriers of autosomal recessive disease had more widespread and more uniform thinning of the glomerular basement membrane (P < 0.0001) and less lamellation (P < 0.04)...
Immunofluorescent patterns produced by antineutrophil cytoplasmic antibodies (ANCA) vary depending on neutrophil substrate and conjugateW Pollock
The University Department of Medicine, Austin and Repatriation Medical Centre, Heidelberg, VIC 3084, Australia
J Clin Pathol 55:680-3. 2002....
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
Department of Human Genetics, Mount Sinai School of Medicine, New York, NY 10029, USA
Am J Hum Genet 69:1033-45. 2001..On the basis of our genetic analyses, the name "MYHIIA syndrome" is proposed to encompass all of these disorders...
