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Journal Abstract Search


193 related items for PubMed ID: 17699467

  • 1. 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. PubMed ID: 17699467
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  • 2. 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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  • 5. 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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  • 7. Varicella as a trigger of atypical haemolytic uraemic syndrome associated with complement dysfunction: two cases.
    Kwon T, Belot A, Ranchin B, Baudouin V, Fremeaux-Bacchi V, Dragon-Durey MA, Cochat P, Loirat C.
    Nephrol Dial Transplant; 2009 Sep; 24(9):2752-4. PubMed ID: 19376828
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  • 8. 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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  • 12. 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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  • 13. The decay accelerating factor mutation I197V found in hemolytic uraemic syndrome does not impair complement regulation.
    Kavanagh D, Burgess R, Spitzer D, Richards A, Diaz-Torres ML, Goodship JA, Hourcade DE, Atkinson JP, Goodship TH.
    Mol Immunol; 2007 May; 44(12):3162-7. PubMed ID: 17368771
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  • 14. Genetic and functional analyses of membrane cofactor protein (CD46) mutations in atypical hemolytic uremic syndrome.
    Fremeaux-Bacchi V, Moulton EA, Kavanagh D, Dragon-Durey MA, Blouin J, Caudy A, Arzouk N, Cleper R, Francois M, Guest G, Pourrat J, Seligman R, Fridman WH, Loirat C, Atkinson JP.
    J Am Soc Nephrol; 2006 Jul; 17(7):2017-25. PubMed ID: 16762990
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  • 15. A mutation in factor I that is associated with atypical hemolytic uremic syndrome does not affect the function of factor I in complement regulation.
    Nilsson SC, Karpman D, Vaziri-Sani F, Kristoffersson AC, Salomon R, Provot F, Fremeaux-Bacchi V, Trouw LA, Blom AM.
    Mol Immunol; 2007 Mar; 44(8):1835-44. PubMed ID: 17084897
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  • 16. Atypical haemolytic uraemic syndrome.
    Kavanagh D, Goodship TH, Richards A.
    Br Med Bull; 2006 Mar; 77-78():5-22. PubMed ID: 16968692
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  • 17. Atypical HUS and complement dysregulation.
    Goodship TH.
    J Am Soc Nephrol; 2006 Jul; 17(7):1775-6. PubMed ID: 16790505
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  • 18. The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome.
    Dragon-Durey MA, Blanc C, Marliot F, Loirat C, Blouin J, Sautes-Fridman C, Fridman WH, Frémeaux-Bacchi V.
    J Med Genet; 2009 Jul; 46(7):447-50. PubMed ID: 19435718
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  • 19. Plasmatherapy in atypical hemolytic uremic syndrome.
    Loirat C, Garnier A, Sellier-Leclerc AL, Kwon T.
    Semin Thromb Hemost; 2010 Sep; 36(6):673-81. PubMed ID: 20865645
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  • 20. Complement dysfunction in hemolytic uremic syndrome.
    Zipfel PF, Skerka C.
    Curr Opin Rheumatol; 2006 Sep; 18(5):548-55. PubMed ID: 16896298
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