Membranoproliferative Glomerulonephritis and C3 Glomerulopathy

Author:

Gale Daniel,Owen-Casey Mared

Publisher

Springer International Publishing

Reference18 articles.

1. Habib R, Michielsen P, et al. In: Wolstenholme GEW, Cameron MP, editors. Clinical, microscopic and electron microscopic data in the nephrotic syndrome of unknown origin. Ciba Foundation Symposium - renal biopsy: clinical and pathological significance. Chichester: John Wiley & Sons Ltd; 1961. p. 70–102.

2. Little MA, Dupont P, et al. Severity of primary MPGN, rather than MPGN type, determines renal survival and post-transplantation recurrence risk. Kidney Int. 2006;69(3):504–11.

3. Servais A, Fremeaux-Bacchi V, et al. Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome. J Med Genet. 2007;44(3):193–9.

4. Walker PD, Ferrario F, et al. Dense deposit disease is not a membranoproliferative glomerulonephritis. Mod Pathol. 2007;20(6):605–16.

5. Abdurrahman MB, Aikhionbare HA, et al. Clinicopathological features of childhood nephrotic syndrome in northern Nigeria. Q J Med. 1990;75(278):563–76.

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