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Items: 1 to 20 of 203

1.

Heterogeneous pattern of renal disease associated with homozygous factor H deficiency.

Servais A, Noël LH, Dragon-Durey MA, Gübler MC, Rémy P, Buob D, Cordonnier C, Makdassi R, Jaber W, Boulanger E, Lesavre P, Frémeaux-Bacchi V.

Hum Pathol. 2011 Sep;42(9):1305-11. doi: 10.1016/j.humpath.2010.11.023. Epub 2011 Mar 10.

PMID:
21396679
2.

Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies.

Servais A, Noël LH, Roumenina LT, Le Quintrec M, Ngo S, Dragon-Durey MA, Macher MA, Zuber J, Karras A, Provot F, Moulin B, Grünfeld JP, Niaudet P, Lesavre P, Frémeaux-Bacchi V.

Kidney Int. 2012 Aug;82(4):454-64. doi: 10.1038/ki.2012.63. Epub 2012 Mar 28.

3.

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.

5.

Membranoproliferative glomerulonephritis with C3NeF and genetic complement dysregulation.

Leroy V, Fremeaux-Bacchi V, Peuchmaur M, Baudouin V, Deschênes G, Macher MA, Loirat C.

Pediatr Nephrol. 2011 Mar;26(3):419-24. doi: 10.1007/s00467-010-1734-4. Epub 2010 Dec 25.

PMID:
21188423
6.

Hereditary and acquired complement dysregulation in membranoproliferative glomerulonephritis.

Licht C, Fremeaux-Bacchi V.

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

PMID:
19190809
7.

Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases.

Dragon-Durey MA, Frémeaux-Bacchi V, Loirat C, Blouin J, Niaudet P, Deschenes G, Coppo P, Herman Fridman W, Weiss L.

J Am Soc Nephrol. 2004 Mar;15(3):787-95.

8.

[Familial membranoproliferative glomerulonephritis].

Bogdanović RM, Dimitrjević JZ, Nikolić VN, Ognjanović MV, Rodić BD, Slavković BV.

Srp Arh Celok Lek. 1999 May-Jun;127(5-6):163-71. Serbian.

PMID:
10500423
10.

Complement factor H deficiency and posttransplantation glomerulonephritis with isolated C3 deposits.

Boyer O, Noël LH, Balzamo E, Guest G, Biebuyck N, Charbit M, Salomon R, Frémeaux-Bacchi V, Niaudet P.

Am J Kidney Dis. 2008 Apr;51(4):671-7. doi: 10.1053/j.ajkd.2007.11.032.

PMID:
18371543
11.

Complement factor H deficiency and endocapillary glomerulonephritis due to paternal isodisomy and a novel factor H mutation.

Schejbel L, Schmidt IM, Kirchhoff M, Andersen CB, Marquart HV, Zipfel P, Garred P.

Genes Immun. 2011 Mar;12(2):90-9. doi: 10.1038/gene.2010.63. Epub 2011 Jan 27.

PMID:
21270828
12.

Heterogeneous histologic and clinical evolution in 3 cases of dense deposit disease with long-term follow-up.

Figuères ML, Frémeaux-Bacchi V, Rabant M, Galmiche L, Marinozzi MC, Grünfeld JP, Noël LH, Servais A.

Hum Pathol. 2014 Nov;45(11):2326-33. doi: 10.1016/j.humpath.2014.07.021. Epub 2014 Aug 16.

PMID:
25260719
13.

Hereditary porcine membranoproliferative glomerulonephritis type II is caused by factor H deficiency.

Høgåsen K, Jansen JH, Mollnes TE, Hovdenes J, Harboe M.

J Clin Invest. 1995 Mar;95(3):1054-61.

14.

Nephritic factors predispose to chronic glomerulonephritis.

West CD.

Am J Kidney Dis. 1994 Dec;24(6):956-63. Review.

PMID:
7985676
15.

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
16.

C3 glomerulonephritis: clinicopathological findings, complement abnormalities, glomerular proteomic profile, treatment, and follow-up.

Sethi S, Fervenza FC, Zhang Y, Zand L, Vrana JA, Nasr SH, Theis JD, Dogan A, Smith RJ.

Kidney Int. 2012 Aug;82(4):465-73.

17.

A case of dense deposit disease associated with a group A streptococcal infection without the involvement of C3NeF or complement factor H deficiency.

Suga K, Kondo S, Matsuura S, Kinoshita Y, Kitano E, Hatanaka M, Kitamura H, Hidaka Y, Oda T, Kagami S.

Pediatr Nephrol. 2010 Aug;25(8):1547-50. doi: 10.1007/s00467-010-1479-0. Epub 2010 Mar 11.

PMID:
20221776
18.

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
19.
20.

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.

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