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Results: 1 to 20 of 156

Similar articles for PubMed (Select 21252520)

1.

Experimental models of membranoproliferative glomerulonephritis, including dense deposit disease.

Vernon KA, Pickering MC, Cook T.

Contrib Nephrol. 2011;169:198-210. doi: 10.1159/000314775. Epub 2011 Jan 20.

PMID:
21252520
2.

In situ complement activation in porcine membranoproliferative glomerulonephritis type II.

Jansen JH, Høgåsen K, Harboe M, Hovig T.

Kidney Int. 1998 Feb;53(2):331-49.

3.

Hereditary and acquired complement dysregulation in membranoproliferative glomerulonephritis.

Licht C, Fremeaux-Bacchi V.

Thromb Haemost. 2009 Feb;101(2):271-8. Review.

PMID:
19190809
6.

Porcine membranoproliferative glomerulonephritis type II: an autosomal recessive deficiency of factor H.

Jansen JH, Høgåsen K, Grøndahl AM.

Vet Rec. 1995 Sep 2;137(10):240-4.

PMID:
8533215
7.

Inherited factor H dysfunction and complement-associated glomerulonephritis in renal grafts of first and second transplantations.

Watanabe S, Yamaguchi Y, Suzuki T, Ikezoe M, Matsumoto N, Chikamoto H, Nagafuchi H, Horita S, Hattori M, Shiraga H, Tokumoto T, Tanabe K, Toma H, Ito K.

Clin Transplant. 2001;15 Suppl 5:45-50.

PMID:
11791795
8.

Uncontrolled C3 activation causes membranoproliferative glomerulonephritis in mice deficient in complement factor H.

Pickering MC, Cook HT, Warren J, Bygrave AE, Moss J, Walport MJ, Botto M.

Nat Genet. 2002 Aug;31(4):424-8. Epub 2002 Jul 1.

PMID:
12091909
9.

Prevention of C5 activation ameliorates spontaneous and experimental glomerulonephritis in factor H-deficient mice.

Pickering MC, Warren J, Rose KL, Carlucci F, Wang Y, Walport MJ, Cook HT, Botto M.

Proc Natl Acad Sci U S A. 2006 Jun 20;103(25):9649-54. Epub 2006 Jun 12.

10.

Histopathology of MPGN and C3 glomerulopathies.

Cook HT, Pickering MC.

Nat Rev Nephrol. 2015 Jan;11(1):14-22. doi: 10.1038/nrneph.2014.217. Epub 2014 Dec 2. Review.

PMID:
25447133
11.

Membranoproliferative glomerulonephritis in dogs with a genetically determined deficiency of the third component of complement.

Cork LC, Morris JM, Olson JL, Krakowka S, Swift AJ, Winkelstein JA.

Clin Immunol Immunopathol. 1991 Sep;60(3):455-70.

PMID:
1864020
12.

Gene polymorphism of complement factor H in a Turkish patient with membranoproliferative glomerulonephritis type II.

Sozeri B, Mir S, Berdeli A, Dincel N, Sarsik B.

Iran J Kidney Dis. 2012 Mar;6(2):149-53.

13.

Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome.

Servais A, Frémeaux-Bacchi V, Lequintrec M, Salomon R, Blouin J, Knebelmann B, Grünfeld JP, Lesavre P, Noël LH, Fakhouri F.

J Med Genet. 2007 Mar;44(3):193-9. Epub 2006 Oct 3.

14.

[Prominent subepithelial deposits detected on 2nd renal biopsy in a boy with membranoproliferative glomerulonephritis type I: a case report].

Motoyama O, Ohshima M, Kawamura S, Iitaka K.

Nihon Jinzo Gakkai Shi. 1995 Apr;37(4):247-52. Japanese.

PMID:
7602812
16.

MPGN II--genetically determined by defective complement regulation?

Licht C, Schlötzer-Schrehardt U, Kirschfink M, Zipfel PF, Hoppe B.

Pediatr Nephrol. 2007 Jan;22(1):2-9. Epub 2006 Sep 23.

PMID:
17024390
17.

Membranoproliferative glomerulonephritis: pathogenetic heterogeneity and proposal for a new classification.

Sethi S, Fervenza FC.

Semin Nephrol. 2011 Jul;31(4):341-8. doi: 10.1016/j.semnephrol.2011.06.005. Review.

PMID:
21839367
18.

[Clinical pathology of the glomerulus--from phenomenon to entity. The membranous lesion].

Langer KH.

Verh Dtsch Ges Pathol. 1989;73:61-70. German.

PMID:
2482636
19.

The alternative pathway C3 convertase and glomerular deposits.

West CD, McAdams AJ.

Pediatr Nephrol. 1999 Jun;13(5):448-53. Review.

PMID:
10412868
20.

A properdin dependent nephritic factor slowly activating C3, C5, and C9 in membranoproliferative glomerulonephritis, types I and III.

Clardy CW, Forristal J, Strife CF, West CD.

Clin Immunol Immunopathol. 1989 Mar;50(3):333-47.

PMID:
2917424
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