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149 related items for PubMed ID: 27268256

  • 1. Chromosomal rearrangement-A rare cause of complement factor I associated atypical haemolytic uraemic syndrome.
    Gleeson PJ, Wilson V, Cox TE, Sharma SD, Smith-Jackson K, Strain L, Lappin D, McHale T, Kavanagh D, Goodship TH.
    Immunobiology; 2016 Oct; 221(10):1124-30. PubMed ID: 27268256
    [Abstract] [Full Text] [Related]

  • 2. 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; 32(6):584-588. PubMed ID: 28455885
    [Abstract] [Full Text] [Related]

  • 3. Thrombotic microangiopathy without renal involvement: two novel mutations in complement-regulator genes.
    Peyvandi F, Rossio R, Ferrari B, Lotta LA, Pontiggia S, Ghiringhelli Borsa N, Pizzuti M, Donadelli R, Piras R, Cugno M, Noris M.
    J Thromb Haemost; 2016 Feb; 14(2):340-5. PubMed ID: 26613809
    [Abstract] [Full Text] [Related]

  • 4. 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; 71():10-22. PubMed ID: 26826462
    [Abstract] [Full Text] [Related]

  • 5. Overactivation of Complement Alternative Pathway in Postpartum Atypical Hemolytic Uremic Syndrome Patients with Renal Involvement.
    Song D, Yu XJ, Wang FM, Xu BN, He YD, Chen Q, Wang SX, Yu F, Song WC, Zhao MH.
    Am J Reprod Immunol; 2015 Oct; 74(4):345-56. PubMed ID: 26011580
    [Abstract] [Full Text] [Related]

  • 6. 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 Oct; 10():853. PubMed ID: 31118930
    [Abstract] [Full Text] [Related]

  • 7. The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome.
    Dragon-Durey MA, Blanc C, Marliot F, Loirat C, Blouin J, Sautes-Fridman C, Fridman WH, Frémeaux-Bacchi V.
    J Med Genet; 2009 Jul; 46(7):447-50. PubMed ID: 19435718
    [Abstract] [Full Text] [Related]

  • 8. Genotype-phenotype correlations of low-frequency variants in the complement system in renal disease and age-related macular degeneration.
    Geerlings MJ, Volokhina EB, de Jong EK, van de Kar N, Pauper M, Hoyng CB, van den Heuvel LP, den Hollander AI.
    Clin Genet; 2018 Oct; 94(3-4):330-338. PubMed ID: 29888403
    [Abstract] [Full Text] [Related]

  • 9. [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]

  • 10. Complement Factor I Variants in Complement-Mediated Renal Diseases.
    Zhang Y, Goodfellow RX, Ghiringhelli Borsa N, Dunlop HC, Presti SA, Meyer NC, Shao D, Roberts SM, Jones MB, Pitcher GR, Taylor AO, Nester CM, Smith RJH.
    Front Immunol; 2022 Apr; 13():866330. PubMed ID: 35619721
    [Abstract] [Full Text] [Related]

  • 11. Genetic Analysis of 400 Patients Refines Understanding and Implicates a New Gene in Atypical Hemolytic Uremic Syndrome.
    Bu F, Zhang Y, Wang K, Borsa NG, Jones MB, Taylor AO, Takanami E, Meyer NC, Frees K, Thomas CP, Nester C, Smith RJH.
    J Am Soc Nephrol; 2018 Dec; 29(12):2809-2819. PubMed ID: 30377230
    [Abstract] [Full Text] [Related]

  • 12. Functional Analysis of Variants in Complement Factor I Identified in Age-Related Macular Degeneration and Atypical Hemolytic Uremic Syndrome.
    de Jong S, de Breuk A, Bakker B, Katti S, Hoyng CB, Nilsson SC, Blom AM, van den Heuvel LP, den Hollander AI, Volokhina EB.
    Front Immunol; 2021 Dec; 12():789897. PubMed ID: 35069568
    [Abstract] [Full Text] [Related]

  • 13. Anti-complement factor I antibody associated atypical hemolytic uremic syndrome - A new insight for future perspective!
    Govindarajan S, Rawat A, Ramachandran R, Hans R, Dawman L, Tiewsoh K.
    Immunobiology; 2020 Sep; 225(5):152000. PubMed ID: 32962820
    [Abstract] [Full Text] [Related]

  • 14. Effect of rare coding variants in the CFI gene on Factor I expression levels.
    de Jong S, Volokhina EB, de Breuk A, Nilsson SC, de Jong EK, van der Kar NCAJ, Bakker B, Hoyng CB, van den Heuvel LP, Blom AM, den Hollander AI.
    Hum Mol Genet; 2020 Aug 11; 29(14):2313-2324. PubMed ID: 32510551
    [Abstract] [Full Text] [Related]

  • 15. Atypical hemolytic uremic syndrome: Korean pediatric series.
    Lee JM, Park YS, Lee JH, Park SJ, Shin JI, Park YH, Yoo KH, Cho MH, Kim SY, Kim SH, Namgoong MK, Lee SJ, Lee JH, Cho HY, Han KH, Kang HG, Ha IS, Bae JS, Kim NK, Park WY, Cheong HI.
    Pediatr Int; 2015 Jun 11; 57(3):431-8. PubMed ID: 25443527
    [Abstract] [Full Text] [Related]

  • 16. Cocaine-associated atypical haemolytic uraemic syndrome in a genetically susceptible individual.
    Bongetti E, Kavanagh D, Martin K, Bendall A, Hill P, Steinberg A, Rajaram Y, Ierino F.
    Nephrology (Carlton); 2020 Jul 11; 25(7):518-521. PubMed ID: 31900968
    [Abstract] [Full Text] [Related]

  • 17. 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 11; 25(7):2195-202. PubMed ID: 20106822
    [Abstract] [Full Text] [Related]

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  • 19. Genetics of atypical hemolytic uremic syndrome (aHUS).
    Rodríguez de Córdoba S, Hidalgo MS, Pinto S, Tortajada A.
    Semin Thromb Hemost; 2014 Jun 11; 40(4):422-30. PubMed ID: 24799305
    [Abstract] [Full Text] [Related]

  • 20. A newly identified mutation in the complement factor I gene not associated with early post-transplant recurrence of atypical hemolytic-uremic syndrome: a case report.
    Ranghino A, Tognarelli G, Basso E, Messina M, Manzione AM, Daidola G, Segoloni GP.
    Transplant Proc; 2013 Sep 11; 45(7):2785-7. PubMed ID: 24034049
    [Abstract] [Full Text] [Related]

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