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Journal Abstract Search

344 related items for PubMed ID: 26911616

  • 1. Diabetic ketoacidosis presenting with atypical hemolytic uremic syndrome associated with a variant of complement factor B in an adult: a case report.
    Zhu Z, Chen H, Gill R, Wang J, Spitalewitz S, Gotlieb V.
    J Med Case Rep; 2016 Feb 24; 10():38. PubMed ID: 26911616
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  • 2. [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 24; 34(2):74-81. PubMed ID: 28682564
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  • 3. Novel Complement Factor B Gene Mutation Identified in a Kidney Transplant Recipient with a Shiga Toxin-Triggered Episode of Thrombotic Microangiopathy.
    Korzycka J, Pawłowicz-Szlarska E, Masajtis-Zagajewska A, Nowicki M.
    Am J Case Rep; 2022 Oct 28; 23():e936565. PubMed ID: 36306276
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  • 4. Mutation of complement factor B causing massive fluid-phase dysregulation of the alternative complement pathway can result in atypical hemolytic uremic syndrome.
    Zhang Y, Kremsdorf RA, Sperati CJ, Henriksen KJ, Mori M, Goodfellow RX, Pitcher GR, Benson CL, Borsa NG, Taylor RP, Nester CM, Smith RJH.
    Kidney Int; 2020 Nov 28; 98(5):1265-1274. PubMed ID: 32540405
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  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. Atypical hemolytic uremic syndrome: a case report.
    Basnayake BMDB, Wazil AWM, Nanayakkara N, Samarakoon SMDK, Senavirathne EMSK, Thangarajah BUEWDR, Karunasena N, Mahanama RMBSS.
    J Med Case Rep; 2020 Jan 13; 14(1):11. PubMed ID: 31928535
    [Abstract] [Full Text] [Related]

  • 7. An extremely rare splice site mutation in the gene encoding complement factor I in a patient with atypical hemolytic uremic syndrome.
    Ipe TS, Lim J, Reyes MA, Ero M, Leveque C, Lewis B, Kain J.
    J Clin Apher; 2017 Dec 13; 32(6):584-588. PubMed ID: 28455885
    [Abstract] [Full Text] [Related]

  • 8. C3 mesangial proliferative glomerulonephritis initially presenting with atypical hemolytic uremic syndrome: a case report.
    Huzmeli C, Candan F, Seker A, Yildiz E, Terzi H, Kayatas M.
    J Med Case Rep; 2016 Jul 27; 10():206. PubMed ID: 27460033
    [Abstract] [Full Text] [Related]

  • 9. Atypical hemolytic uremic syndrome and acute tubular necrosis induced by complement factor B gene (CFB) mutation: A case report.
    Wu H, Su S, Li L, Zhang L.
    Medicine (Baltimore); 2021 Mar 19; 100(11):e25069. PubMed ID: 33725982
    [Abstract] [Full Text] [Related]

  • 10. Atypical Hemolytic Uremic Syndrome Presenting as Acute Heart Failure-A Rare Presentation: Diagnosis Supported by Skin Biopsy.
    Kichloo A, Chugh SS, Gupta S, Pandav J, Chander P.
    J Investig Med High Impact Case Rep; 2019 Mar 19; 7():2324709619842905. PubMed ID: 31010328
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  • 15. Rare genetic variant in the CFB gene presenting as atypical hemolytic uremic syndrome and immune complex diffuse membranoproliferative glomerulonephritis, with crescents, successfully treated with eculizumab.
    Alfakeeh K, Azar M, Alfadhel M, Abdullah AM, Aloudah N, Alsaad KO.
    Pediatr Nephrol; 2017 May 19; 32(5):885-891. PubMed ID: 28210841
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  • 19. Hemolytic uremic syndrome with multiple organ involvement secondary to complement factor H p.Arg1215X mutation.
    Yeşilbaş O, Şevketoğlu E, Petmezci MT, Kıhtır HS, Benzer M, Berdeli A.
    Turk J Pediatr; 2017 May 19; 59(5):576-580. PubMed ID: 29745120
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