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Journal Abstract Search

157 related items for PubMed ID: 28167400

  • 1. Postpartum atypical hemolytic uremic syndrome with complement factor H mutation complicated by reversible cerebrovascular constriction syndrome successfully treated with eculizumab.
    Yamaguchi M, Hori M, Hiroshi N, Maruyama S.
    Thromb Res; 2017 Mar; 151():79-81. PubMed ID: 28167400
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  • 5. Atypical Hemolytic Uremic Syndrome Associated with Complement Factor H Mutation and IgA Nephropathy: A Case Report Successfully Treated with Eculizumab.
    Nakamura H, Anayama M, Makino M, Makino Y, Tamura K, Nagasawa M.
    Nephron; 2018 Mar; 138(4):324-327. PubMed ID: 29241200
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  • 6. Plasma resistant atypical hemolytic uremic syndrome associated with a CFH mutation treated with eculizumab: a case report.
    Sevinc M, Basturk T, Sahutoglu T, Sakaci T, Koc Y, Ahbap E, Akgol C, Kara E, Brocklebank V, Goodship TH, Kavanagh D, Unsal A.
    J Med Case Rep; 2015 Apr 29; 9():92. PubMed ID: 25925370
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  • 7. Prophylactic eculizumab for kidney transplantation in a child with atypical hemolytic uremic syndrome due to complement factor H mutation.
    Ranch D, Crowther B, Arar M, Assanasen C.
    Pediatr Transplant; 2014 Sep 29; 18(6):E185-9. PubMed ID: 24931815
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  • 8. Eculizumab for the treatment of an atypical hemolytic uremic syndrome with mutations in complement factor I and C3.
    Ferreira E, Oliveira N, Marques M, Francisco L, Santos A, Carreira A, Campos M.
    Nefrologia; 2016 Sep 29; 36(1):72-5. PubMed ID: 26541438
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  • 9. Discontinuation of Eculizumab in a Patient With Atypical Hemolytic Uremic Syndrome Due to a Mutation in CFH.
    Habbig S, Bergmann C, Weber LT.
    Am J Kidney Dis; 2016 Mar 29; 67(3):532-3. PubMed ID: 26724167
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  • 11. A complicated case of atypical hemolytic uremic syndrome with frequent relapses under eculizumab.
    Schalk G, Kirschfink M, Wehling C, Gastoldi S, Bergmann C, Hoppe B, Weber LT.
    Pediatr Nephrol; 2015 Jun 29; 30(6):1039-42. PubMed ID: 25752761
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  • 12. [Atypical hemolytic uremic syndrome with C3 p.I1157T missense mutation successfully treated with eculizumab].
    Okano M, Matsumoto T, Nakamori Y, Ino K, Miyazaki K, Fujieda A, Sugimoto Y, Tawara I, Yamaguchi M, Ohishi K, Miwa H, Masuya M, Wada H, Katayama N.
    Rinsho Ketsueki; 2018 Jun 29; 59(2):178-181. PubMed ID: 29515070
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  • 16. Thrombotic Microangiopathy with Complement Factor H Gene Mutations Unassociated with Atypical Hemolytic Uremic Syndrome.
    Oymak Y, Karapınar TH, Ay Y, Özcan E, Müminoğlu N, Aydın Köker S, Töret E, Berdeli A, Serdaroğlu E, Vergin C.
    Turk J Haematol; 2015 Sep 29; 32(3):275-6. PubMed ID: 26376595
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  • 20. [Human genetics in atypical hemolytic uremic syndrome-its role in diagnosis and treatment].
    Knoop M, Haller H, Menne J.
    Internist (Berl); 2018 Aug 29; 59(8):799-804. PubMed ID: 29995248
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