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151 related items for PubMed ID: 21881555

  • 1. Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significance.
    Tortajada A, Pinto S, Martínez-Ara J, López-Trascasa M, Sánchez-Corral P, de Córdoba SR.
    Kidney Int; 2012 Jan; 81(1):56-63. PubMed ID: 21881555
    [Abstract] [Full Text] [Related]

  • 2. Complement factor H, FHR-3 and FHR-1 variants associate in an extended haplotype conferring increased risk of atypical hemolytic uremic syndrome.
    Bernabéu-Herrero ME, Jiménez-Alcázar M, Anter J, Pinto S, Sánchez Chinchilla D, Garrido S, López-Trascasa M, Rodríguez de Córdoba S, Sánchez-Corral P.
    Mol Immunol; 2015 Oct; 67(2 Pt B):276-86. PubMed ID: 26163426
    [Abstract] [Full Text] [Related]

  • 3. Characterization of complement factor H-related (CFHR) proteins in plasma reveals novel genetic variations of CFHR1 associated with atypical hemolytic uremic syndrome.
    Abarrategui-Garrido C, Martínez-Barricarte R, López-Trascasa M, de Córdoba SR, Sánchez-Corral P.
    Blood; 2009 Nov 05; 114(19):4261-71. PubMed ID: 19745068
    [Abstract] [Full Text] [Related]

  • 4. Tissue-specific host recognition by complement factor H is mediated by differential activities of its glycosaminoglycan-binding regions.
    Clark SJ, Ridge LA, Herbert AP, Hakobyan S, Mulloy B, Lennon R, Würzner R, Morgan BP, Uhrín D, Bishop PN, Day AJ.
    J Immunol; 2013 Mar 01; 190(5):2049-57. PubMed ID: 23365078
    [Abstract] [Full Text] [Related]

  • 5. Membrano-proliferative glomerulonephritis, atypical hemolytic uremic syndrome, and a new complement factor H mutation: report of a case.
    Gnappi E, Allinovi M, Vaglio A, Bresin E, Sorosina A, Pilato FP, Allegri L, Manenti L.
    Pediatr Nephrol; 2012 Oct 01; 27(10):1995-9. PubMed ID: 22669321
    [Abstract] [Full Text] [Related]

  • 6. 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 01; 46(8-9):1573-94. PubMed ID: 19297022
    [Abstract] [Full Text] [Related]

  • 7. Spontaneous hemolytic uremic syndrome triggered by complement factor H lacking surface recognition domains.
    Pickering MC, de Jorge EG, Martinez-Barricarte R, Recalde S, Garcia-Layana A, Rose KL, Moss J, Walport MJ, Cook HT, de Córdoba SR, Botto M.
    J Exp Med; 2007 Jun 11; 204(6):1249-56. PubMed ID: 17517971
    [Abstract] [Full Text] [Related]

  • 8. Complement factor H-related protein 1 deficiency and factor H antibodies in pediatric patients with atypical hemolytic uremic syndrome.
    Hofer J, Janecke AR, Zimmerhackl LB, Riedl M, Rosales A, Giner T, Cortina G, Haindl CJ, Petzelberger B, Pawlik M, Jeller V, Vester U, Gadner B, van Husen M, Moritz ML, Würzner R, Jungraithmayr T, German-Austrian HUS Study Group.
    Clin J Am Soc Nephrol; 2013 Mar 11; 8(3):407-15. PubMed ID: 23243267
    [Abstract] [Full Text] [Related]

  • 9. Functional Characterization of Rare Genetic Variants in the N-Terminus of Complement Factor H in aHUS, C3G, and AMD.
    Wong EKS, Hallam TM, Brocklebank V, Walsh PR, Smith-Jackson K, Shuttleworth VG, Cox TE, Anderson HE, Barlow PN, Marchbank KJ, Harris CL, Kavanagh D.
    Front Immunol; 2020 Mar 11; 11():602284. PubMed ID: 33519811
    [Abstract] [Full Text] [Related]

  • 10. Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype.
    Bresin E, Rurali E, Caprioli J, Sanchez-Corral P, Fremeaux-Bacchi V, Rodriguez de Cordoba S, Pinto S, Goodship TH, Alberti M, Ribes D, Valoti E, Remuzzi G, Noris M, European Working Party on Complement Genetics in Renal Diseases.
    J Am Soc Nephrol; 2013 Feb 11; 24(3):475-86. PubMed ID: 23431077
    [Abstract] [Full Text] [Related]

  • 11. Retinal disease in the C3 glomerulopathies and the risk of impaired vision.
    Savige J, Amos L, Ierino F, Mack HG, Symons RC, Hughes P, Nicholls K, Colville D.
    Ophthalmic Genet; 2016 Dec 11; 37(4):369-376. PubMed ID: 26915021
    [Abstract] [Full Text] [Related]

  • 12. Genetic analysis and functional characterization of novel mutations in a series of patients with atypical hemolytic uremic syndrome.
    Szarvas N, Szilágyi Á, Csuka D, Takács B, Rusai K, Müller T, Arbeiter K, Réti M, Haris Á, Wagner L, Török S, Kelen K, Szabó AJ, Reusz GS, Morgan BP, Prohászka Z.
    Mol Immunol; 2016 Mar 11; 71():10-22. PubMed ID: 26826462
    [Abstract] [Full Text] [Related]

  • 13. Factor I autoantibodies in patients with atypical hemolytic uremic syndrome: disease-associated or an epiphenomenon?
    Kavanagh D, Pappworth IY, Anderson H, Hayes CM, Moore I, Hunze EM, Bennaceur K, Roversi P, Lea S, Strain L, Ward R, Plant N, Nailescu C, Goodship TH, Marchbank KJ.
    Clin J Am Soc Nephrol; 2012 Mar 11; 7(3):417-26. PubMed ID: 22223611
    [Abstract] [Full Text] [Related]

  • 14. Variations in the complement regulatory genes factor H (CFH) and factor H related 5 (CFHR5) are associated with membranoproliferative glomerulonephritis type II (dense deposit disease).
    Abrera-Abeleda MA, Nishimura C, Smith JL, Sethi S, McRae JL, Murphy BF, Silvestri G, Skerka C, Józsi M, Zipfel PF, Hageman GS, Smith RJ.
    J Med Genet; 2006 Jul 11; 43(7):582-9. PubMed ID: 16299065
    [Abstract] [Full Text] [Related]

  • 15. Complete functional characterization of disease-associated genetic variants in the complement factor H gene.
    Merinero HM, García SP, García-Fernández J, Arjona E, Tortajada A, Rodríguez de Córdoba S.
    Kidney Int; 2018 Feb 11; 93(2):470-481. PubMed ID: 28941939
    [Abstract] [Full Text] [Related]

  • 16. A haplotype in CFH family genes confers high risk of rare glomerular nephropathies.
    Ding Y, Zhao W, Zhang T, Qiang H, Lu J, Su X, Wen S, Xu F, Zhang M, Zhang H, Zeng C, Liu Z, Chen H.
    Sci Rep; 2017 Jul 20; 7(1):6004. PubMed ID: 28729648
    [Abstract] [Full Text] [Related]

  • 17. 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 20; 28(3):222-34. PubMed ID: 17089378
    [Abstract] [Full Text] [Related]

  • 18. The complement factor H R1210C mutation is associated with atypical hemolytic uremic syndrome.
    Martinez-Barricarte R, Pianetti G, Gautard R, Misselwitz J, Strain L, Fremeaux-Bacchi V, Skerka C, Zipfel PF, Goodship T, Noris M, Remuzzi G, de Cordoba SR, European Working Party on the Genetics of HUS.
    J Am Soc Nephrol; 2008 Mar 20; 19(3):639-46. PubMed ID: 18235085
    [Abstract] [Full Text] [Related]

  • 19. Atypical hemolytic uremic syndrome: telling the difference between H and Y.
    Goicoechea de Jorge E, Pickering MC.
    Kidney Int; 2010 Oct 20; 78(8):721-3. PubMed ID: 20877372
    [Abstract] [Full Text] [Related]

  • 20. Factor H genotype-phenotype correlations: lessons from aHUS, MPGN II, and AMD.
    Goodship TH.
    Kidney Int; 2006 Jul 20; 70(1):12-3. PubMed ID: 16810287
    [Abstract] [Full Text] [Related]

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