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537 related items for PubMed ID: 17089378

  • 1. The interactive Factor H-atypical hemolytic uremic syndrome mutation database and website: update and integration of membrane cofactor protein and Factor I mutations with structural models.
    Saunders RE, Abarrategui-Garrido C, Frémeaux-Bacchi V, Goicoechea de Jorge E, Goodship TH, López Trascasa M, Noris M, Ponce Castro IM, Remuzzi G, Rodríguez de Córdoba S, Sánchez-Corral P, Skerka C, Zipfel PF, Perkins SJ.
    Hum Mutat; 2007 Mar; 28(3):222-34. PubMed ID: 17089378
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  • 2. An interactive web database of factor H-associated hemolytic uremic syndrome mutations: insights into the structural consequences of disease-associated mutations.
    Saunders RE, Goodship TH, Zipfel PF, Perkins SJ.
    Hum Mutat; 2006 Jan; 27(1):21-30. PubMed ID: 16281287
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  • 3. A user's guide to the interactive Web database of factor H-associated hemolytic uremic syndrome.
    Saunders RE, Perkins SJ.
    Semin Thromb Hemost; 2006 Mar; 32(2):160-8. PubMed ID: 16575691
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  • 6. Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome.
    Sellier-Leclerc AL, Fremeaux-Bacchi V, Dragon-Durey MA, Macher MA, Niaudet P, Guest G, Boudailliez B, Bouissou F, Deschenes G, Gie S, Tsimaratos M, Fischbach M, Morin D, Nivet H, Alberti C, Loirat C, French Society of Pediatric Nephrology.
    J Am Soc Nephrol; 2007 Aug; 18(8):2392-400. PubMed ID: 17599974
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  • 10. 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. PubMed ID: 16575689
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  • 11. Genetic disorders in complement (regulating) genes in patients with atypical haemolytic uraemic syndrome (aHUS).
    Westra D, Volokhina E, van der Heijden E, Vos A, Huigen M, Jansen J, van Kaauwen E, van der Velden T, van de Kar N, van den Heuvel L.
    Nephrol Dial Transplant; 2010 Jul; 25(7):2195-202. PubMed ID: 20106822
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  • 12. Atypical haemolytic uraemic syndrome.
    Kavanagh D, Goodship TH, Richards A.
    Br Med Bull; 2006 Jul; 77-78():5-22. PubMed ID: 16968692
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  • 16. Unusual clinical severity of complement membrane cofactor protein-associated hemolytic-uremic syndrome and uniparental isodisomy.
    Fremeaux-Bacchi V, Sanlaville D, Menouer S, Blouin J, Dragon-Durey MA, Fischbach M, Vekemans M, Fridman WH.
    Am J Kidney Dis; 2007 Feb; 49(2):323-9. PubMed ID: 17261436
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  • 17. Atypical hemolytic uremic syndrome: update on the complement system and what is new.
    Hirt-Minkowski P, Dickenmann M, Schifferli JA.
    Nephron Clin Pract; 2010 Feb; 114(4):c219-35. PubMed ID: 20090363
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  • 18. Inherited deficiency of membrane cofactor protein expression and varying manifestations of recurrent atypical hemolytic uremic syndrome in a sibling pair.
    Couzi L, Contin-Bordes C, Marliot F, Sarrat A, Grimal P, Moreau JF, Merville P, Fremeaux-Bacchi V.
    Am J Kidney Dis; 2008 Aug; 52(2):e5-9. PubMed ID: 18514989
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  • 20. 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. PubMed ID: 20865641
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