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Journal Abstract Search

231 related items for PubMed ID: 32553244

  • 61. [Atypical hemolytic uremic syndrome with C3 p.I1157T missense mutation successfully treated with eculizumab].
    Okano M, Matsumoto T, Nakamori Y, Ino K, Miyazaki K, Fujieda A, Sugimoto Y, Tawara I, Yamaguchi M, Ohishi K, Miwa H, Masuya M, Wada H, Katayama N.
    Rinsho Ketsueki; 2018; 59(2):178-181. PubMed ID: 29515070
    [Abstract] [Full Text] [Related]

  • 62.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Martín B, Smith RJH.
    ; 1993. PubMed ID: 20301598
    [Abstract] [Full Text] [Related]

  • 63. Anti-factor H autoantibodies in C3 glomerulopathies and in atypical hemolytic uremic syndrome: one target, two diseases.
    Blanc C, Togarsimalemath SK, Chauvet S, Le Quintrec M, Moulin B, Buchler M, Jokiranta TS, Roumenina LT, Fremeaux-Bacchi V, Dragon-Durey MA.
    J Immunol; 2015 Jun 01; 194(11):5129-38. PubMed ID: 25917093
    [Abstract] [Full Text] [Related]

  • 64. CFHR Gene Variations Provide Insights in the Pathogenesis of the Kidney Diseases Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy.
    Zipfel PF, Wiech T, Stea ED, Skerka C.
    J Am Soc Nephrol; 2020 Feb 01; 31(2):241-256. PubMed ID: 31980588
    [Abstract] [Full Text] [Related]

  • 65. Pathology of renal diseases associated with dysfunction of the alternative pathway of complement: C3 glomerulopathy and atypical hemolytic uremic syndrome (aHUS).
    Sethi S, Fervenza FC.
    Semin Thromb Hemost; 2014 Jun 01; 40(4):416-21. PubMed ID: 24799306
    [Abstract] [Full Text] [Related]

  • 66. Clinical characteristics and genetic backgrounds of Japanese patients with atypical hemolytic uremic syndrome.
    Fujisawa M, Kato H, Yoshida Y, Usui T, Takata M, Fujimoto M, Wada H, Uchida Y, Kokame K, Matsumoto M, Fujimura Y, Miyata T, Nangaku M.
    Clin Exp Nephrol; 2018 Oct 01; 22(5):1088-1099. PubMed ID: 29511899
    [Abstract] [Full Text] [Related]

  • 67. Analysis of patients with atypical hemolytic uremic syndrome treated at the Mie University Hospital: concentration of C3 p.I1157T mutation.
    Matsumoto T, Fan X, Ishikawa E, Ito M, Amano K, Toyoda H, Komada Y, Ohishi K, Katayama N, Yoshida Y, Matsumoto M, Fujimura Y, Ikejiri M, Wada H, Miyata T.
    Int J Hematol; 2014 Nov 01; 100(5):437-42. PubMed ID: 25135378
    [Abstract] [Full Text] [Related]

  • 68. [Atypical HUS caused by complement-related abnormalities].
    Yoshida Y, Matsumoto M.
    Rinsho Ketsueki; 2015 Feb 01; 56(2):185-93. PubMed ID: 25765799
    [Abstract] [Full Text] [Related]

  • 69. Atypical hemolytic uremic syndrome with C3 mutation: A case report and literature review.
    Liu J, Xiao J, Chen L, Peng Y.
    Clin Nephrol; 2021 Mar 01; 95(3):156-160. PubMed ID: 33210998
    [Abstract] [Full Text] [Related]

  • 70. 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]

  • 71. Hot Spot of Complement Factor I Rare Variant p.Ile357Met in Patients With Hemolytic Uremic Syndrome.
    Schwotzer N, Fakhouri F, Martins PV, Delmas Y, Caillard S, Zuber J, Moranne O, Mesnard L, Frémeaux-Bacchi V, El-Sissy C.
    Am J Kidney Dis; 2024 Aug 10; 84(2):244-249. PubMed ID: 38423159
    [Abstract] [Full Text] [Related]

  • 72. Contribution of functional and quantitative genetic variants of Complement Factor H and Factor H-Related (FHR) proteins on renal pathology.
    Gómez Delgado I, Sánchez-Corral P.
    Nefrologia (Engl Ed); 2022 Aug 10; 42(3):280-289. PubMed ID: 36154806
    [Abstract] [Full Text] [Related]

  • 73. A complement factor B mutation in a large kindred with atypical hemolytic uremic syndrome.
    Funato M, Uemura O, Ushijima K, Ohnishi H, Orii K, Kato Z, Yamakawa S, Nagai T, Ohara O, Kaneko H, Kondo N.
    J Clin Immunol; 2014 Aug 10; 34(6):691-5. PubMed ID: 24906628
    [Abstract] [Full Text] [Related]

  • 74.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 75. Disturbed sialic acid recognition on endothelial cells and platelets in complement attack causes atypical hemolytic uremic syndrome.
    Hyvärinen S, Meri S, Jokiranta TS.
    Blood; 2016 Jun 02; 127(22):2701-10. PubMed ID: 27006390
    [Abstract] [Full Text] [Related]

  • 76. Clinical characterization and identification of rare genetic variants in atypical hemolytic uremic syndrome: A Swedish retrospective observational study.
    Åkesson A, Martin M, Blom AM, Rossing M, Gabrielaite M, Zetterberg E, Klintman J.
    Ther Apher Dial; 2021 Dec 02; 25(6):988-1000. PubMed ID: 33609329
    [Abstract] [Full Text] [Related]

  • 77.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 78. Atypical haemolytic uraemic syndrome with underlying glomerulopathies. A case series and a review of the literature.
    Manenti L, Gnappi E, Vaglio A, Allegri L, Noris M, Bresin E, Pilato FP, Valoti E, Pasquali S, Buzio C.
    Nephrol Dial Transplant; 2013 Sep 02; 28(9):2246-59. PubMed ID: 23787552
    [Abstract] [Full Text] [Related]

  • 79. Genotypic analysis of a large cohort of patients with suspected atypical hemolytic uremic syndrome.
    Connaughton DM, Bhai P, Isenring P, Mahdi M, Sadikovic B, Schenkel LC.
    J Mol Med (Berl); 2023 Aug 02; 101(8):1029-1040. PubMed ID: 37466676
    [Abstract] [Full Text] [Related]

  • 80. Whole-exome sequencing detects mutations in pediatric patients with atypical hemolytic uremic syndrome in Taiwan.
    Tseng MH, Tsai JD, Tsai IJ, Huang SM, Huang JL, Fan WL, Lee HJ, Wu TW, Lin SH.
    Clin Chim Acta; 2019 Jul 02; 494():143-150. PubMed ID: 30905589
    [Abstract] [Full Text] [Related]

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