These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
6. The molecular and structural bases for the association of complement C3 mutations with atypical hemolytic uremic syndrome. Martínez-Barricarte R; Heurich M; López-Perrote A; Tortajada A; Pinto S; López-Trascasa M; Sánchez-Corral P; Morgan BP; Llorca O; Harris CL; Rodríguez de Córdoba S Mol Immunol; 2015 Aug; 66(2):263-73. PubMed ID: 25879158 [TBL] [Abstract][Full Text] [Related]
7. Atypical haemolytic uraemic syndrome and mutations in complement regulator genes. Dragon-Durey MA; Frémeaux-Bacchi V Springer Semin Immunopathol; 2005 Nov; 27(3):359-74. PubMed ID: 16189652 [TBL] [Abstract][Full Text] [Related]
9. 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; 17(7):2017-25. PubMed ID: 16762990 [TBL] [Abstract][Full Text] [Related]
10. Complement factor H deficiency and posttransplantation glomerulonephritis with isolated C3 deposits. Boyer O; Noël LH; Balzamo E; Guest G; Biebuyck N; Charbit M; Salomon R; Frémeaux-Bacchi V; Niaudet P Am J Kidney Dis; 2008 Apr; 51(4):671-7. PubMed ID: 18371543 [TBL] [Abstract][Full Text] [Related]
11. Varicella as a trigger of atypical haemolytic uraemic syndrome associated with complement dysfunction: two cases. Kwon T; Belot A; Ranchin B; Baudouin V; Fremeaux-Bacchi V; Dragon-Durey MA; Cochat P; Loirat C Nephrol Dial Transplant; 2009 Sep; 24(9):2752-4. PubMed ID: 19376828 [TBL] [Abstract][Full Text] [Related]
12. Inherited deficiency of membrane cofactor protein expression and varying manifestations of recurrent atypical hemolytic uremic syndrome in a sibling pair. Couzi L; Contin-Bordes C; Marliot F; Sarrat A; Grimal P; Moreau JF; Merville P; Fremeaux-Bacchi V Am J Kidney Dis; 2008 Aug; 52(2):e5-9. PubMed ID: 18514989 [TBL] [Abstract][Full Text] [Related]
13. Successful kidney transplant with eculizumab, thymoglobulin and belatacept therapy in a highly-sensitised patient with atypical haemolytic uraemic syndrome due to factor H mutation. Nieto-Ríos JF; Zuluaga-Quintero M; Bello-Márquez DC; Aristizabal-Alzate A; Ocampo-Kohn C; Serna-Higuita LM; Arias L; Zuluaga-Valencia G Nefrologia (Engl Ed); 2018; 38(4):433-437. PubMed ID: 29778558 [TBL] [Abstract][Full Text] [Related]
14. 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; 44(1-3):111-22. PubMed ID: 16882452 [TBL] [Abstract][Full Text] [Related]
15. A 'silent', new polymorphism of factor H and apparent de novo atypical haemolytic uraemic syndrome after kidney transplantation. Broeders EN; Stordeur P; Rorive S; Dahan K BMJ Case Rep; 2014 Dec; 2014():. PubMed ID: 25538218 [TBL] [Abstract][Full Text] [Related]
16. Atypical haemolytic uraemic syndrome: a case of rare genetic mutation. Sangeetha G; Jayaraj J; Ganesan S; Puttagunta S BMJ Case Rep; 2021 Jul; 14(7):. PubMed ID: 34330731 [TBL] [Abstract][Full Text] [Related]
17. A novel CD46 mutation in a patient with microangiopathy clinically resembling thrombotic thrombocytopenic purpura and normal ADAMTS13 activity. Rossio R; Lotta LA; Pontiggia S; Borsa NG; Garagiola I; Ardissino G; Mikovic D; Cugno M; Peyvandi F Haematologica; 2015 Mar; 100(3):e87-9. PubMed ID: 25381125 [No Abstract] [Full Text] [Related]
18. 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; 25(7):2195-202. PubMed ID: 20106822 [TBL] [Abstract][Full Text] [Related]
19. Defining the genetics of thrombotic microangiopathies. Vieira-Martins P; El Sissy C; Bordereau P; Gruber A; Rosain J; Fremeaux-Bacchi V Transfus Apher Sci; 2016 Apr; 54(2):212-9. PubMed ID: 27177491 [TBL] [Abstract][Full Text] [Related]
20. Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome. Servais A; Frémeaux-Bacchi V; Lequintrec M; Salomon R; Blouin J; Knebelmann B; Grünfeld JP; Lesavre P; Noël LH; Fakhouri F J Med Genet; 2007 Mar; 44(3):193-9. PubMed ID: 17018561 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]