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Journal Abstract Search

126 related items for PubMed ID: 21868097

  • 1. 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; 49(1-2):48-55. PubMed ID: 21868097
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries.
    Neumann HP, Salzmann M, Bohnert-Iwan B, Mannuelian T, Skerka C, Lenk D, Bender BU, Cybulla M, Riegler P, Königsrainer A, Neyer U, Bock A, Widmer U, Male DA, Franke G, Zipfel PF.
    J Med Genet; 2003 Sep; 40(9):676-81. PubMed ID: 12960213
    [Abstract] [Full Text] [Related]

  • 4. The complement factor H R1210C mutation is associated with atypical hemolytic uremic syndrome.
    Martinez-Barricarte R, Pianetti G, Gautard R, Misselwitz J, Strain L, Fremeaux-Bacchi V, Skerka C, Zipfel PF, Goodship T, Noris M, Remuzzi G, de Cordoba SR, European Working Party on the Genetics of HUS.
    J Am Soc Nephrol; 2008 Mar; 19(3):639-46. PubMed ID: 18235085
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. 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]

  • 7. Complement factor H, FHR-3 and FHR-1 variants associate in an extended haplotype conferring increased risk of atypical hemolytic uremic syndrome.
    Bernabéu-Herrero ME, Jiménez-Alcázar M, Anter J, Pinto S, Sánchez Chinchilla D, Garrido S, López-Trascasa M, Rodríguez de Córdoba S, Sánchez-Corral P.
    Mol Immunol; 2015 Oct; 67(2 Pt B):276-86. PubMed ID: 26163426
    [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; 24(3):475-86. PubMed ID: 23431077
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. 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]

  • 11. High Complement Factor H-Related (FHR)-3 Levels Are Associated With the Atypical Hemolytic-Uremic Syndrome-Risk Allele CFHR3*B.
    Pouw RB, Gómez Delgado I, López Lera A, Rodríguez de Córdoba S, Wouters D, Kuijpers TW, Sánchez-Corral P.
    Front Immunol; 2018 Oct; 9():848. PubMed ID: 29740447
    [Abstract] [Full Text] [Related]

  • 12. Clustering of missense mutations in the C-terminal region of factor H in atypical hemolytic uremic syndrome.
    Pérez-Caballero D, González-Rubio C, Gallardo ME, Vera M, López-Trascasa M, Rodríguez de Córdoba S, Sánchez-Corral P.
    Am J Hum Genet; 2001 Feb; 68(2):478-84. PubMed ID: 11170895
    [Abstract] [Full Text] [Related]

  • 13. Insights into hemolytic uremic syndrome: segregation of three independent predisposition factors in a large, multiple affected pedigree.
    Esparza-Gordillo J, Jorge EG, Garrido CA, Carreras L, López-Trascasa M, Sánchez-Corral P, de Córdoba SR.
    Mol Immunol; 2006 Apr; 43(11):1769-75. PubMed ID: 16386793
    [Abstract] [Full Text] [Related]

  • 14. Atypical hemolytic uremic syndrome: telling the difference between H and Y.
    Goicoechea de Jorge E, Pickering MC.
    Kidney Int; 2010 Oct; 78(8):721-3. PubMed ID: 20877372
    [Abstract] [Full Text] [Related]

  • 15. Interpretation of genetic variants of uncertain significance in atypical hemolytic uremic syndrome.
    Kavanagh D, Anderson HE.
    Kidney Int; 2012 Jan; 81(1):11-3. PubMed ID: 22170528
    [Abstract] [Full Text] [Related]

  • 16. 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; 57(3):431-8. PubMed ID: 25443527
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. [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]

  • 19. Partial ADAMTS13 deficiency in atypical hemolytic uremic syndrome.
    Feng S, Eyler SJ, Zhang Y, Maga T, Nester CM, Kroll MH, Smith RJ, Afshar-Kharghan V.
    Blood; 2013 Aug 22; 122(8):1487-93. PubMed ID: 23847193
    [Abstract] [Full Text] [Related]

  • 20. The interactive Factor H-atypical hemolytic uremic syndrome mutation database and website: update and integration of membrane cofactor protein and Factor I mutations with structural models.
    Saunders RE, Abarrategui-Garrido C, Frémeaux-Bacchi V, Goicoechea de Jorge E, Goodship TH, López Trascasa M, Noris M, Ponce Castro IM, Remuzzi G, Rodríguez de Córdoba S, Sánchez-Corral P, Skerka C, Zipfel PF, Perkins SJ.
    Hum Mutat; 2007 Mar 22; 28(3):222-34. PubMed ID: 17089378
    [Abstract] [Full Text] [Related]

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