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Items: 18

1.

Common genetic variants in complement genes other than CFH, CD46 and the CFHRs are not associated with aHUS.

Ermini L, Goodship TH, Strain L, Weale ME, Sacks SH, Cordell HJ, Fremeaux-Bacchi V, Sheerin NS.

Mol Immunol. 2012 Jan;49(4):640-8. doi: 10.1016/j.molimm.2011.11.003. Epub 2011 Dec 5.

2.

Complement activation in diseases presenting with thrombotic microangiopathy.

Meri S.

Eur J Intern Med. 2013 Sep;24(6):496-502. doi: 10.1016/j.ejim.2013.05.009. Epub 2013 Jun 4. Review.

PMID:
23743117
3.

Atypical hemolytic uremic syndrome associated with mutations in complement regulator genes.

Le Quintrec M, Roumenina L, Noris M, Frémeaux-Bacchi V.

Semin Thromb Hemost. 2010 Sep;36(6):641-52. doi: 10.1055/s-0030-1262886. Epub 2010 Sep 23. Review.

PMID:
20865641
4.

Implications of the initial mutations in membrane cofactor protein (MCP; CD46) leading to atypical hemolytic uremic syndrome.

Richards A, Kathryn Liszewski M, Kavanagh D, Fang CJ, Moulton E, Fremeaux-Bacchi V, Remuzzi G, Noris M, Goodship TH, Atkinson JP.

Mol Immunol. 2007 Jan;44(1-3):111-22. Epub 2006 Aug 1. Review.

PMID:
16882452
5.

Screening for complement system abnormalities in patients with atypical hemolytic uremic syndrome.

Kavanagh D, Richards A, Fremeaux-Bacchi V, Noris M, Goodship T, Remuzzi G, Atkinson JP.

Clin J Am Soc Nephrol. 2007 May;2(3):591-6. Epub 2007 Feb 14. Review. No abstract available.

6.

Atypical haemolytic uraemic syndrome and mutations in complement regulator genes.

Dragon-Durey MA, Frémeaux-Bacchi V.

Springer Semin Immunopathol. 2005 Nov;27(3):359-74. Epub 2005 Nov 11. Review.

PMID:
16189652
7.

Atypical haemolytic uraemic syndrome.

Kavanagh D, Goodship TH, Richards A.

Br Med Bull. 2006;77-78:5-22. Epub 2006 Sep 11. Review.

PMID:
16968692
8.

Complement factor H related proteins (CFHRs).

Skerka C, Chen Q, Fremeaux-Bacchi V, Roumenina LT.

Mol Immunol. 2013 Dec 15;56(3):170-80. doi: 10.1016/j.molimm.2013.06.001. Epub 2013 Jul 3. Review.

9.

Atypical hemolytic uremic syndrome: update on the complement system and what is new.

Hirt-Minkowski P, Dickenmann M, Schifferli JA.

Nephron Clin Pract. 2010;114(4):c219-35. doi: 10.1159/000276545. Epub 2010 Jan 14. Review.

10.

Mutations in CD46, a complement regulatory protein, predispose to atypical HUS.

Goodship TH, Liszewski MK, Kemp EJ, Richards A, Atkinson JP.

Trends Mol Med. 2004 May;10(5):226-31. Review.

PMID:
15121049
11.

Atypical haemolytic uraemic syndrome with underlying glomerulopathies. A case series and a review of the literature.

Manenti L, Gnappi E, Vaglio A, Allegri L, Noris M, Bresin E, Pilato FP, Valoti E, Pasquali S, Buzio C.

Nephrol Dial Transplant. 2013 Sep;28(9):2246-59. doi: 10.1093/ndt/gft220. Epub 2013 Jun 19. Review.

12.

Genetics of atypical hemolytic uremic syndrome (aHUS).

Rodríguez de Córdoba S, Hidalgo MS, Pinto S, Tortajada A.

Semin Thromb Hemost. 2014 Jun;40(4):422-30. doi: 10.1055/s-0034-1375296. Epub 2014 May 5. Review.

PMID:
24799305
13.

Complement regulatory genes and hemolytic uremic syndromes.

Kavanagh D, Richards A, Atkinson J.

Annu Rev Med. 2008;59:293-309. Review.

PMID:
17705684
14.

The role of defective complement control in hemolytic uremic syndrome.

Zipfel PF, Misselwitz J, Licht C, Skerka C.

Semin Thromb Hemost. 2006 Mar;32(2):146-54. Review.

PMID:
16575689
15.

The spectrum of phenotypes caused by variants in the CFH gene.

Boon CJ, van de Kar NC, Klevering BJ, Keunen JE, Cremers FP, Klaver CC, Hoyng CB, Daha MR, den Hollander AI.

Mol Immunol. 2009 May;46(8-9):1573-94. doi: 10.1016/j.molimm.2009.02.013. Epub 2009 Mar 17. Review.

PMID:
19297022
16.

Complement regulator CD46: genetic variants and disease associations.

Liszewski MK, Atkinson JP.

Hum Genomics. 2015 Jun 10;9:7. doi: 10.1186/s40246-015-0029-z. Review.

17.

Factor H-related proteins.

Józsi M, Meri S.

Methods Mol Biol. 2014;1100:225-36. doi: 10.1007/978-1-62703-724-2_18. Review.

PMID:
24218263
18.

Inhibiting complement activation on cells at the step of C3 cleavage.

Liszewski MK, Fang CJ, Atkinson JP.

Vaccine. 2008 Dec 30;26 Suppl 8:I22-7. Review.

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