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6. Increased alternative pathway regulation by using an anti complement regulator factor H potentiating antibody

9. Heterogeneity but individual constancy of epitopes, isotypes and avidity of factor H autoantibodies in atypical hemolytic uremic syndrome

10. Complement factor H, FHR-3 and FHR-1 variants associate in an extended haplotype conferring increased risk of atypical hemolytic uremic syndrome

11. The molecular and structural bases for the association of complement C3 mutations with atypical hemolytic uremic syndrome

17. Proteomics-based discovery of an abnormal, internally duplicated CFHR1 protein which associates with renal pathology in a Spanish family

18. Factor H autoantibodies in a Hemolytic Uremic Syndrome patient presenting homozygous CFHR1 and CFHR4A deficiency

20. Identification and functional characterisation of a relatively frequent CFH haplotype carrying two polymorphisms (S890I and V1007L) associated with aHUS

25. Novel complement factor H mutation in SCR7 in a patient with age-related macular degeneration and membranoproliferative glomerulonephritis type II

28. Mutations in complement factor B are associated with atypical hemolytic uremic syndrome

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