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Journal Abstract Search

205 related items for PubMed ID: 23314101

  • 1. 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; 54(2):238-46. PubMed ID: 23314101
    [Abstract] [Full Text] [Related]

  • 2. 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; 5(10):1844-59. PubMed ID: 20595690
    [Abstract] [Full Text] [Related]

  • 3. A novel quantitative hemolytic assay coupled with restriction fragment length polymorphisms analysis enabled early diagnosis of atypical hemolytic uremic syndrome and identified unique predisposing mutations in Japan.
    Yoshida Y, Miyata T, Matsumoto M, Shirotani-Ikejima H, Uchida Y, Ohyama Y, Kokubo T, Fujimura Y.
    PLoS One; 2015 Oct; 10(5):e0124655. PubMed ID: 25951460
    [Abstract] [Full Text] [Related]

  • 4. Complement factor H-related protein 1 deficiency and factor H antibodies in pediatric patients with atypical hemolytic uremic syndrome.
    Hofer J, Janecke AR, Zimmerhackl LB, Riedl M, Rosales A, Giner T, Cortina G, Haindl CJ, Petzelberger B, Pawlik M, Jeller V, Vester U, Gadner B, van Husen M, Moritz ML, Würzner R, Jungraithmayr T, German-Austrian HUS Study Group.
    Clin J Am Soc Nephrol; 2013 Mar; 8(3):407-15. PubMed ID: 23243267
    [Abstract] [Full Text] [Related]

  • 5. Atypical hemolytic uremic syndrome.
    Loirat C, Frémeaux-Bacchi V.
    Orphanet J Rare Dis; 2011 Sep 08; 6():60. PubMed ID: 21902819
    [Abstract] [Full Text] [Related]

  • 6. [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 08; 32(4):232-40. PubMed ID: 21376430
    [Abstract] [Full Text] [Related]

  • 7. 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 Apr 08; 43(3):160-9. PubMed ID: 27064621
    [Abstract] [Full Text] [Related]

  • 8. 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 08; 24(3):475-86. PubMed ID: 23431077
    [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 08; 71():10-22. PubMed ID: 26826462
    [Abstract] [Full Text] [Related]

  • 10. 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 08; 100(5):437-42. PubMed ID: 25135378
    [Abstract] [Full Text] [Related]

  • 11. 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 08; 27(1):73-81. PubMed ID: 21706448
    [Abstract] [Full Text] [Related]

  • 12. Thrombomodulin mutations in atypical hemolytic-uremic syndrome.
    Delvaeye M, Noris M, De Vriese A, Esmon CT, Esmon NL, Ferrell G, Del-Favero J, Plaisance S, Claes B, Lambrechts D, Zoja C, Remuzzi G, Conway EM.
    N Engl J Med; 2009 Jul 23; 361(4):345-57. PubMed ID: 19625716
    [Abstract] [Full Text] [Related]

  • 13. 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 23; 49(1-2):48-55. PubMed ID: 21868097
    [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 Oct 23; 114(4):c219-35. PubMed ID: 20090363
    [Abstract] [Full Text] [Related]

  • 15. Clinical and Genetic Characteristics of Atypical Hemolytic Uremic Syndrome in Children: A Chinese Cohort Study.
    Wu D, Chen J, Ling C, Chen Z, Fan J, Sun Q, Meng Q, Liu X.
    Nephron; 2021 Oct 23; 145(4):415-427. PubMed ID: 33873197
    [Abstract] [Full Text] [Related]

  • 16. 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 23; 22(5):1088-1099. PubMed ID: 29511899
    [Abstract] [Full Text] [Related]

  • 17. Membrane cofactor protein mutations in atypical hemolytic uremic syndrome (aHUS), fatal Stx-HUS, C3 glomerulonephritis, and the HELLP syndrome.
    Fang CJ, Fremeaux-Bacchi V, Liszewski MK, Pianetti G, Noris M, Goodship TH, Atkinson JP.
    Blood; 2008 Jan 15; 111(2):624-32. PubMed ID: 17914026
    [Abstract] [Full Text] [Related]

  • 18. Rare Functional Variants in Complement Genes and Anti-FH Autoantibodies-Associated aHUS.
    Valoti E, Alberti M, Iatropoulos P, Piras R, Mele C, Breno M, Cremaschi A, Bresin E, Donadelli R, Alizzi S, Amoroso A, Benigni A, Remuzzi G, Noris M.
    Front Immunol; 2019 Jan 15; 10():853. PubMed ID: 31118930
    [Abstract] [Full Text] [Related]

  • 19. Genetic and functional analyses of membrane cofactor protein (CD46) mutations in atypical hemolytic uremic syndrome.
    Fremeaux-Bacchi V, Moulton EA, Kavanagh D, Dragon-Durey MA, Blouin J, Caudy A, Arzouk N, Cleper R, Francois M, Guest G, Pourrat J, Seligman R, Fridman WH, Loirat C, Atkinson JP.
    J Am Soc Nephrol; 2006 Jul 15; 17(7):2017-25. PubMed ID: 16762990
    [Abstract] [Full Text] [Related]

  • 20. Implications of the initial mutations in membrane cofactor protein (MCP; CD46) leading to atypical hemolytic uremic syndrome.
    Richards A, Kathryn Liszewski M, Kavanagh D, Fang CJ, Moulton E, Fremeaux-Bacchi V, Remuzzi G, Noris M, Goodship TH, Atkinson JP.
    Mol Immunol; 2007 Jan 15; 44(1-3):111-22. PubMed ID: 16882452
    [Abstract] [Full Text] [Related]

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