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Journal Abstract Search

183 related items for PubMed ID: 20108004

  • 1. A novel mutation in the complement factor B gene (CFB) and atypical hemolytic uremic syndrome.
    Tawadrous H, Maga T, Sharma J, Kupferman J, Smith RJ, Schoeneman M.
    Pediatr Nephrol; 2010 May; 25(5):947-51. PubMed ID: 20108004
    [Abstract] [Full Text] [Related]

  • 2. [Atypical hemolytic-uremic syndrome related to abnormalities within the complement system].
    Frémeaux-Bacchi V, Fakhouri F, Roumenina L, Dragon-Durey MA, Loirat C.
    Rev Med Interne; 2011 Apr; 32(4):232-40. PubMed ID: 21376430
    [Abstract] [Full Text] [Related]

  • 3. 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; 32(5):885-891. PubMed ID: 28210841
    [Abstract] [Full Text] [Related]

  • 4. 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; 24(3):475-86. PubMed ID: 23431077
    [Abstract] [Full Text] [Related]

  • 5. Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome.
    Maga TK, Nishimura CJ, Weaver AE, Frees KL, Smith RJ.
    Hum Mutat; 2010 Jun; 31(6):E1445-60. PubMed ID: 20513133
    [Abstract] [Full Text] [Related]

  • 6. Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome.
    Goicoechea de Jorge E, Harris CL, Esparza-Gordillo J, Carreras L, Arranz EA, Garrido CA, López-Trascasa M, Sánchez-Corral P, Morgan BP, Rodríguez de Córdoba S.
    Proc Natl Acad Sci U S A; 2007 Jan 02; 104(1):240-5. PubMed ID: 17182750
    [Abstract] [Full Text] [Related]

  • 7. 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 02; 34(6):691-5. PubMed ID: 24906628
    [Abstract] [Full Text] [Related]

  • 8. Manifestation of atypical hemolytic uremic syndrome caused by novel mutations in MCP.
    Provaznikova D, Rittich S, Malina M, Seeman T, Marinov I, Riedl M, Hrachovinova I.
    Pediatr Nephrol; 2012 Jan 02; 27(1):73-81. PubMed ID: 21706448
    [Abstract] [Full Text] [Related]

  • 9. 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 02; 71():10-22. PubMed ID: 26826462
    [Abstract] [Full Text] [Related]

  • 10. 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 02; 13(3):663-75. PubMed ID: 23356914
    [Abstract] [Full Text] [Related]

  • 11. Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome.
    Frémeaux-Bacchi V, Miller EC, Liszewski MK, Strain L, Blouin J, Brown AL, Moghal N, Kaplan BS, Weiss RA, Lhotta K, Kapur G, Mattoo T, Nivet H, Wong W, Gie S, Hurault de Ligny B, Fischbach M, Gupta R, Hauhart R, Meunier V, Loirat C, Dragon-Durey MA, Fridman WH, Janssen BJ, Goodship TH, Atkinson JP.
    Blood; 2008 Dec 15; 112(13):4948-52. PubMed ID: 18796626
    [Abstract] [Full Text] [Related]

  • 12. Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype.
    Noris M, Caprioli J, Bresin E, Mossali C, Pianetti G, Gamba S, Daina E, Fenili C, Castelletti F, Sorosina A, Piras R, Donadelli R, Maranta R, van der Meer I, Conway EM, Zipfel PF, Goodship TH, Remuzzi G.
    Clin J Am Soc Nephrol; 2010 Oct 15; 5(10):1844-59. PubMed ID: 20595690
    [Abstract] [Full Text] [Related]

  • 13. Atypical hemolytic uremic syndrome in children: complement mutations and clinical characteristics.
    Geerdink LM, Westra D, van Wijk JA, Dorresteijn EM, Lilien MR, Davin JC, Kömhoff M, Van Hoeck K, van der Vlugt A, van den Heuvel LP, van de Kar NC.
    Pediatr Nephrol; 2012 Aug 15; 27(8):1283-91. PubMed ID: 22410797
    [Abstract] [Full Text] [Related]

  • 14. Atypical hemolytic uremic syndrome: update on the complement system and what is new.
    Hirt-Minkowski P, Dickenmann M, Schifferli JA.
    Nephron Clin Pract; 2010 Aug 15; 114(4):c219-35. PubMed ID: 20090363
    [Abstract] [Full Text] [Related]

  • 15. 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 15; 27(10):1995-9. PubMed ID: 22669321
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. 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 19; 77(4):339-49. PubMed ID: 20016463
    [Abstract] [Full Text] [Related]

  • 18. Rapid recovery of membrane cofactor protein (MCP; CD46) associated atypical haemolytic uraemic syndrome with plasma exchange.
    Reid VL, Mullan A, Erwig LP.
    BMJ Case Rep; 2013 Sep 04; 2013():. PubMed ID: 24005975
    [Abstract] [Full Text] [Related]

  • 19. 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 04; 25(7):2195-202. PubMed ID: 20106822
    [Abstract] [Full Text] [Related]

  • 20. Update on evaluating complement in hemolytic uremic syndrome.
    Kavanagh D, Goodship TH.
    Curr Opin Nephrol Hypertens; 2007 Nov 04; 16(6):565-71. PubMed ID: 18089972
    [Abstract] [Full Text] [Related]

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