CD80 and suPAR in patients with minimal change disease and focal segmental glomerulosclerosis: diagnostic and pathogenic significance

Author:

Cara-Fuentes Gabriel,Wei Changli,Segarra Alfons,Ishimoto Takuji,Rivard Christopher,Johnson Richard J.,Reiser Jochen,Garin Eduardo H.

Publisher

Springer Science and Business Media LLC

Subject

Nephrology,Pediatrics, Perinatology, and Child Health

Reference19 articles.

1. Habib R, Kleinknecht C (1971) The primary nephrotic syndrome in childhood: classification and clinicopathologic study of 406 cases. Pathol Annu 6:417–474

2. Barisoni L, Schnaper HW, Kopp JB (2007) A proposed taxonomy for the podocytopathies: a reassessment of the primary nephrotic diseases. Clin J Am Soc Nephrol 2:529–542

3. Kriz W, LeHir M (2005) Pathways to nephron loss starting from glomerular diseases-insights from animal models. Kidney Int 67:404–419

4. Ponticelli C, Glassock RJ (2010) Treatment of primary glomerulonephritis, 2nd edn. Oxford University Press, New York, p 181

5. Shalhoub RJ (1974) Pathogenesis of lipoid nephrosis: a disorder of T-cell function. Lancet 2:556–560

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