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Journal Abstract Search

367 related items for PubMed ID: 26826462

  • 61. 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
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  • 62. 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
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  • 63. Atypical hemolytic uremic syndrome recurrence after kidney transplantation.
    Matar D, Naqvi F, Racusen LC, Carter-Monroe N, Montgomery RA, Alachkar N.
    Transplantation; 2014 Dec 15; 98(11):1205-12. PubMed ID: 24933457
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  • 65. Overactivity of Alternative Pathway Convertases in Patients With Complement-Mediated Renal Diseases.
    Michels MAHM, van de Kar NCAJ, Okrój M, Blom AM, van Kraaij SAW, Volokhina EB, van den Heuvel LPWJ.
    Front Immunol; 2018 Dec 15; 9():612. PubMed ID: 29670616
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  • 66. 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
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  • 67. 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 Aug 15; 145(4):415-427. PubMed ID: 33873197
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  • 68. Atypical hemolytic uremic syndrome and genetic aberrations in the complement factor H-related 5 gene.
    Westra D, Vernon KA, Volokhina EB, Pickering MC, van de Kar NC, van den Heuvel LP.
    J Hum Genet; 2012 Jul 15; 57(7):459-64. PubMed ID: 22622361
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  • 70. 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 15; 28(3):222-34. PubMed ID: 17089378
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  • 71. Targeted exome sequencing in anti-factor H antibody negative HUS reveals multiple variations.
    Thergaonkar RW, Narang A, Gurjar BS, Tiwari P, Puraswani M, Saini H, Sinha A, Varma B, Mukerji M, Hari P, Bagga A.
    Clin Exp Nephrol; 2018 Jun 15; 22(3):653-660. PubMed ID: 28939980
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  • 72. Anti-complement factor H (CFH) antibodies and a novel CFH gene mutation in an atypical hemolytic uremic syndrome patient with complement activation of the classical pathway.
    Minato S, Iijima H, Nakao H, Nishi K, Hidaka Y, Inoue N, Kubota M, Ishiguro A.
    Immunol Med; 2021 Dec 15; 44(4):274-277. PubMed ID: 33784485
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  • 73. Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome.
    Mele C, Lemaire M, Iatropoulos P, Piras R, Bresin E, Bettoni S, Bick D, Helbling D, Veith R, Valoti E, Donadelli R, Murer L, Neunhäuserer M, Breno M, Frémeaux-Bacchi V, Lifton R, Remuzzi G, Noris M.
    Clin J Am Soc Nephrol; 2015 Jun 05; 10(6):1011-9. PubMed ID: 25854283
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  • 79. Clinical characterization and identification of rare genetic variants in atypical hemolytic uremic syndrome: A Swedish retrospective observational study.
    Åkesson A, Martin M, Blom AM, Rossing M, Gabrielaite M, Zetterberg E, Klintman J.
    Ther Apher Dial; 2021 Dec 05; 25(6):988-1000. PubMed ID: 33609329
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  • 80. [Atypical HUS caused by complement-related abnormalities].
    Yoshida Y, Matsumoto M.
    Rinsho Ketsueki; 2015 Feb 05; 56(2):185-93. PubMed ID: 25765799
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