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Journal Abstract Search

367 related items for PubMed ID: 26826462

  • 41. Mutations in components of complement influence the outcome of Factor I-associated atypical hemolytic uremic syndrome.
    Bienaime F, Dragon-Durey MA, Regnier CH, Nilsson SC, Kwan WH, Blouin J, Jablonski M, Renault N, Rameix-Welti MA, Loirat C, Sautés-Fridman C, Villoutreix BO, Blom AM, Fremeaux-Bacchi V.
    Kidney Int; 2010 Feb; 77(4):339-49. PubMed ID: 20016463
    [Abstract] [Full Text] [Related]

  • 42. Complement activation in diseases presenting with thrombotic microangiopathy.
    Meri S.
    Eur J Intern Med; 2013 Sep; 24(6):496-502. PubMed ID: 23743117
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  • 43. Age-related penetrance of hereditary atypical hemolytic uremic syndrome.
    Sullivan M, Rybicki LA, Winter A, Hoffmann MM, Reiermann S, Linke H, Arbeiter K, Patzer L, Budde K, Hoppe B, Zeier M, Lhotta K, Bock A, Wiech T, Gaspert A, Fehr T, Woznowski M, Berisha G, Malinoc A, Goek ON, Eng C, Neumann HP.
    Ann Hum Genet; 2011 Nov; 75(6):639-47. PubMed ID: 21906045
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  • 44. A novel missense mutation in complement factor I predisposes patients to atypical hemolytic uremic syndrome: a case report.
    Wei X, Li J, Zhan X, Tu L, Huang H, Wang Y.
    J Med Case Rep; 2022 Mar 04; 16(1):101. PubMed ID: 35241161
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  • 45. Atypical hemolytic uremic syndrome: telling the difference between H and Y.
    Goicoechea de Jorge E, Pickering MC.
    Kidney Int; 2010 Oct 04; 78(8):721-3. PubMed ID: 20877372
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  • 46. [Complement factor B mutation in atypical hemolytic uremic syndrome. Rare cause of rare disease].
    Visconti L, Cernaro V, Ardissino G, Sgarbanti M, Ferrara D, Visconti G, Santoro D, Buemi M.
    G Ital Nefrol; 2017 Apr 04; 34(2):74-81. PubMed ID: 28682564
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  • 47. Chromosomal rearrangement-A rare cause of complement factor I associated atypical haemolytic uraemic syndrome.
    Gleeson PJ, Wilson V, Cox TE, Sharma SD, Smith-Jackson K, Strain L, Lappin D, McHale T, Kavanagh D, Goodship TH.
    Immunobiology; 2016 Oct 04; 221(10):1124-30. PubMed ID: 27268256
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  • 48. A novel atypical hemolytic uremic syndrome-associated hybrid CFHR1/CFH gene encoding a fusion protein that antagonizes factor H-dependent complement regulation.
    Valoti E, Alberti M, Tortajada A, Garcia-Fernandez J, Gastoldi S, Besso L, Bresin E, Remuzzi G, Rodriguez de Cordoba S, Noris M.
    J Am Soc Nephrol; 2015 Jan 04; 26(1):209-19. PubMed ID: 24904082
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  • 49. Comprehensive Analysis of Complement Genes in Patients with Atypical Hemolytic Uremic Syndrome.
    Zhang T, Lu J, Liang S, Chen D, Zhang H, Zeng C, Liu Z, Chen H.
    Am J Nephrol; 2016 Jan 04; 43(3):160-9. PubMed ID: 27064621
    [Abstract] [Full Text] [Related]

  • 50. 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 04; 7(3):417-26. PubMed ID: 22223611
    [Abstract] [Full Text] [Related]

  • 51. Case report: A family of atypical hemolytic uremic syndrome involving a CFH::CFHR1 fusion gene and CFHR3-1-4-2 gene duplication.
    Tasaki Y, Tsujimoto H, Yokoyama T, Sugimoto N, Kitajima S, Fujii H, Hidaka Y, Kato N, Maruyama S, Inoue N, Wada T.
    Front Immunol; 2024 Mar 04; 15():1360855. PubMed ID: 38524137
    [Abstract] [Full Text] [Related]

  • 52. Genetic and Protein Structural Evaluation of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy.
    Perkins SJ.
    Adv Chronic Kidney Dis; 2020 Mar 04; 27(2):120-127.e4. PubMed ID: 32553244
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  • 53. CFH-CFHR1 hybrid genes in two cases of atypical hemolytic uremic syndrome.
    Sugawara Y, Kato H, Nagasaki M, Yoshida Y, Fujisawa M, Minegishi N, Yamamoto M, Nangaku M.
    J Hum Genet; 2023 Jun 04; 68(6):427-430. PubMed ID: 36755127
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  • 54. Distinct genetic profile with recurrent population-specific missense variants in Korean adult atypical hemolytic uremic syndrome.
    Yun JW, Oh J, Lee KO, Lee SJ, Kim JO, Kim NK, Kim JS, Koh Y, Yoon SS, Yhim HY, Jo SK, Park Y, Lee JE, Park J, Lee JW, Kim SH, Kim HJ, Oh D, Korean TTP Registry investigators, aHUS working group.
    Thromb Res; 2020 Oct 04; 194():45-53. PubMed ID: 33213850
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  • 55. Kidney Transplantation in Patients with Atypical Hemolytic Uremic Syndrome due to Complement Factor H Deficiency: Impact of Liver Transplantation.
    Kim S, Park E, Min SI, Yi NJ, Ha J, Ha IS, Cheong HI, Kang HG.
    J Korean Med Sci; 2018 Jan 01; 33(1):e4. PubMed ID: 29215813
    [Abstract] [Full Text] [Related]

  • 56. Complement Factor I Variants in Complement-Mediated Renal Diseases.
    Zhang Y, Goodfellow RX, Ghiringhelli Borsa N, Dunlop HC, Presti SA, Meyer NC, Shao D, Roberts SM, Jones MB, Pitcher GR, Taylor AO, Nester CM, Smith RJH.
    Front Immunol; 2022 Jan 01; 13():866330. PubMed ID: 35619721
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  • 57. CFH and CFHR structural variants in atypical Hemolytic Uremic Syndrome: Prevalence, genomic characterization and impact on outcome.
    Piras R, Valoti E, Alberti M, Bresin E, Mele C, Breno M, Liguori L, Donadelli R, Rigoldi M, Benigni A, Remuzzi G, Noris M.
    Front Immunol; 2022 Jan 01; 13():1011580. PubMed ID: 36793547
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  • 58. Favorable long-term outcomes of isolated liver transplantation in a child with atypical hemolytic uremic syndrome caused by a novel complement factor H mutation
.
    Cho H, Lee Y.
    Clin Nephrol; 2017 Jul 01; 88(1):52-56. PubMed ID: 28502324
    [Abstract] [Full Text] [Related]

  • 59. The role of complement in Streptococcus pneumoniae-associated haemolytic uraemic syndrome.
    Szilágyi A, Kiss N, Bereczki C, Tálosi G, Rácz K, Túri S, Györke Z, Simon E, Horváth E, Kelen K, Reusz GS, Szabó AJ, Tulassay T, Prohászka Z.
    Nephrol Dial Transplant; 2013 Sep 01; 28(9):2237-45. PubMed ID: 23787556
    [Abstract] [Full Text] [Related]

  • 60. Molecular Studies and an ex vivo Complement Assay on Endothelium Highlight the Genetic Complexity of Atypical Hemolytic Uremic Syndrome: The Case of a Pedigree With a Null CD46 Variant.
    Piras R, Iatropoulos P, Bresin E, Todeschini M, Gastoldi S, Valoti E, Alberti M, Mele C, Galbusera M, Cuccarolo P, Benigni A, Remuzzi G, Noris M.
    Front Med (Lausanne); 2020 Sep 01; 7():579418. PubMed ID: 33224962
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