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Journal Abstract Search

189 related items for PubMed ID: 20877372

  • 21. Atypical hemolytic uremic syndrome associated with complement factor H autoantibodies and CFHR1/CFHR3 deficiency.
    Lee BH, Kwak SH, Shin JI, Lee SH, Choi HJ, Kang HG, Ha IS, Lee JS, Dragon-Durey MA, Choi Y, Cheong HI.
    Pediatr Res; 2009 Sep; 66(3):336-40. PubMed ID: 19531976
    [Abstract] [Full Text] [Related]

  • 22. Epidemiological approach to identifying genetic predispositions for atypical hemolytic uremic syndrome.
    Sullivan M, Erlic Z, Hoffmann MM, Arbeiter K, Patzer L, Budde K, Hoppe B, Zeier M, Lhotta K, Rybicki LA, Bock A, Berisha G, Neumann HP.
    Ann Hum Genet; 2010 Jan; 74(1):17-26. PubMed ID: 20059470
    [Abstract] [Full Text] [Related]

  • 23. 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. PubMed ID: 24799305
    [Abstract] [Full Text] [Related]

  • 24. 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; 19(3):639-46. PubMed ID: 18235085
    [Abstract] [Full Text] [Related]

  • 25. 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]

  • 26. Functional characterization of two novel non-synonymous alterations in CD46 and a Q950H change in factor H found in atypical hemolytic uremic syndrome patients.
    Mohlin FC, Nilsson SC, Levart TK, Golubovic E, Rusai K, Müller-Sacherer T, Arbeiter K, Pállinger É, Szarvas N, Csuka D, Szilágyi Á, Villoutreix BO, Prohászka Z, Blom AM.
    Mol Immunol; 2015 Jun 01; 65(2):367-76. PubMed ID: 25733390
    [Abstract] [Full Text] [Related]

  • 27. Factor H gene variants in Japanese: its relation to atypical hemolytic uremic syndrome.
    Mukai S, Hidaka Y, Hirota-Kawadobora M, Matsuda K, Fujihara N, Takezawa Y, Kubota S, Koike K, Honda T, Yamauchi K.
    Mol Immunol; 2011 Oct 01; 49(1-2):48-55. PubMed ID: 21868097
    [Abstract] [Full Text] [Related]

  • 28. Haemolytic uraemic syndrome caused by factor H mutation: is single kidney transplantation under intensive plasmatherapy an option?
    Hirt-Minkowski P, Schaub S, Mayr M, Schifferli JA, Dickenmann M, Frémeaux-Bacchi V, Steiger J.
    Nephrol Dial Transplant; 2009 Nov 01; 24(11):3548-51. PubMed ID: 19633317
    [Abstract] [Full Text] [Related]

  • 29. Analysis of genetic and predisposing factors in Japanese patients with atypical hemolytic uremic syndrome.
    Fan X, Yoshida Y, Honda S, Matsumoto M, Sawada Y, Hattori M, Hisanaga S, Hiwa R, Nakamura F, Tomomori M, Miyagawa S, Fujimaru R, Yamada H, Sawai T, Ikeda Y, Iwata N, Uemura O, Matsukuma E, Aizawa Y, Harada H, Wada H, Ishikawa E, Ashida A, Nangaku M, Miyata T, Fujimura Y.
    Mol Immunol; 2013 Jun 01; 54(2):238-46. PubMed ID: 23314101
    [Abstract] [Full Text] [Related]

  • 30. Recurrent atypical hemolytic uremic syndrome associated with factor I mutation in a living related renal transplant recipient.
    Chan MR, Thomas CP, Torrealba JR, Djamali A, Fernandez LA, Nishimura CJ, Smith RJ, Samaniego MD.
    Am J Kidney Dis; 2009 Feb 01; 53(2):321-6. PubMed ID: 18805611
    [Abstract] [Full Text] [Related]

  • 31. Interpretation of genetic variants of uncertain significance in atypical hemolytic uremic syndrome.
    Kavanagh D, Anderson HE.
    Kidney Int; 2012 Jan 01; 81(1):11-3. PubMed ID: 22170528
    [Abstract] [Full Text] [Related]

  • 32. 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 01; 81(1):56-63. PubMed ID: 21881555
    [Abstract] [Full Text] [Related]

  • 33. Successful therapeutic plasma exchange in a 3.2-kg body weight neonate with atypical hemolytic uremic syndrome.
    Jung S, Kang ES, Ki CS, Kim DW, Paik KH, Chang YS.
    J Clin Apher; 2011 Jan 01; 26(3):162-5. PubMed ID: 21322001
    [Abstract] [Full Text] [Related]

  • 34. 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 01; 25(7):2195-202. PubMed ID: 20106822
    [Abstract] [Full Text] [Related]

  • 35. Complement genes strongly predict recurrence and graft outcome in adult renal transplant recipients with atypical hemolytic and uremic syndrome.
    Le Quintrec M, Zuber J, Moulin B, Kamar N, Jablonski M, Lionet A, Chatelet V, Mousson C, Mourad G, Bridoux F, Cassuto E, Loirat C, Rondeau E, Delahousse M, Frémeaux-Bacchi V.
    Am J Transplant; 2013 Mar 01; 13(3):663-75. PubMed ID: 23356914
    [Abstract] [Full Text] [Related]

  • 36. 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]

  • 37. Distal Angiopathy and Atypical Hemolytic Uremic Syndrome: Clinical and Functional Properties of an Anti-Factor H IgAλ Antibody.
    Rigothier C, Delmas Y, Roumenina LT, Contin-Bordes C, Lepreux S, Bridoux F, Goujon JM, Bachelet T, Touchard G, Frémeaux-Bacchi V, Combe C.
    Am J Kidney Dis; 2015 Aug 11; 66(2):331-6. PubMed ID: 26015278
    [Abstract] [Full Text] [Related]

  • 38. A novel hybrid CFH/CFHR3 gene generated by a microhomology-mediated deletion in familial atypical hemolytic uremic syndrome.
    Francis NJ, McNicholas B, Awan A, Waldron M, Reddan D, Sadlier D, Kavanagh D, Strain L, Marchbank KJ, Harris CL, Goodship TH.
    Blood; 2012 Jan 12; 119(2):591-601. PubMed ID: 22058112
    [Abstract] [Full Text] [Related]

  • 39. Atypical haemolytic uraemic syndrome associated with a hybrid complement gene.
    Venables JP, Strain L, Routledge D, Bourn D, Powell HM, Warwicker P, Diaz-Torres ML, Sampson A, Mead P, Webb M, Pirson Y, Jackson MS, Hughes A, Wood KM, Goodship JA, Goodship TH.
    PLoS Med; 2006 Oct 12; 3(10):e431. PubMed ID: 17076561
    [Abstract] [Full Text] [Related]

  • 40. The major autoantibody epitope on factor H in atypical hemolytic uremic syndrome is structurally different from its homologous site in factor H-related protein 1, supporting a novel model for induction of autoimmunity in this disease.
    Bhattacharjee A, Reuter S, Trojnár E, Kolodziejczyk R, Seeberger H, Hyvärinen S, Uzonyi B, Szilágyi Á, Prohászka Z, Goldman A, Józsi M, Jokiranta TS.
    J Biol Chem; 2015 Apr 10; 290(15):9500-10. PubMed ID: 25659429
    [Abstract] [Full Text] [Related]

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