The Oxford classification of IgA nephropathy: rationale, clinicopathological correlations, and classification.

By D. Cattran, R. Coppo, H. Cook, J. Feehally, I. Roberts, S. Troyanov, C. Alpers, A. Amore, J. Barratt, F. Berthoux and 35 more. Kidney International, 2009

1,192 citations recorded by the source corpus.

Subfields: Nephrology, Pathology and Forensic Medicine

View Paper: https://www.semanticscholar.org/paper/351bb6a9dda77a94302ead96ad411dc42709bafe

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

1. Kai-Uwe Eckardt
2. T. Goodship
3. M. Noris
4. B. Kasiske
5. L. Roumenina
6. V. Frémeaux-Bacchi
7. H. Cook
8. C. Licht

Citations in the corpus

• The Oxford classification of IgA nephropathy: pathology definitions, correlations, and reproducibility. (2009, background): “As described in the accompanying paper 17 , we sought to develop an international consensus classification of IgA nephropathy with a strong evidence base.”
• Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a "Kidney Disease: Improving Global Outcomes" (KDIGO) Controversies Conference. (2017, methodology): “A comprehensive study is needed to define the relationship of morphology to etiology, clinical course, and response to therapy, which would be best achieved by a multicenter collection of well-annotated cases, analyzed by a group of renal pathologists in a manner similar to that used for the Oxford ”
• KDIGO Clinical Practice Guideline for Glomerulonephritis (2012, background): “K There is low-quality evidence to suggest kidney biopsy findings associated with a worse prognosis are the presence and severity of mesangial and endocapillary proliferation, extensive crescents, focal and segmental as well as global glomerulosclerosis, tubular atrophy, and interstitial fibrosis.(4”