List of works - Pilar Sánchez-Corral

Anti-factor H antibody affecting factor H cofactor activity in a patient with dense deposit disease.

scientific article published on 15 March 2012

Atypical aHUS: State of the art.

scientific article

Atypical hemolytic uremic syndrome-associated variants and autoantibodies impair binding of factor h and factor h-related protein 1 to pentraxin 3.

scientific article

Characterization of complement factor H-related (CFHR) proteins in plasma reveals novel genetic variations of CFHR1 associated with atypical hemolytic uremic syndrome

scientific article

Complement Genetic Variants and FH Desialylation in <i>S. pneumoniae</i>-Haemolytic Uraemic Syndrome

scientific article published on 11 March 2021

Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significance

scientific article

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

scientific article

Complement mutations in diacylglycerol kinase-ε-associated atypical hemolytic uremic syndrome

scientific article

Eculizumab long-term therapy for pediatric renal transplant in aHUS with CFH/CFHR1 hybrid gene

scientific article

Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome

scientific article

Insights into hemolytic uremic syndrome: segregation of three independent predisposition factors in a large, multiple affected pedigree

scientific article

Mutations in proteins of the alternative pathway of complement and the pathogenesis of atypical hemolytic uremic syndrome

scientific article

Potentiation of complement regulator factor H protects human endothelial cells from complement attack in aHUS sera

scientific article published on 01 February 2019

Predisposition to atypical hemolytic uremic syndrome involves the concurrence of different susceptibility alleles in the regulators of complement activation gene cluster in 1q32.

scientific article

Structural and functional characterization of factor H mutations associated with atypical hemolytic uremic syndrome

scientific article

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

scientific article

List of works by Pilar Sánchez-Corral

Anti-factor H antibody affecting factor H cofactor activity in a patient with dense deposit disease.

Atypical aHUS: State of the art.

Atypical hemolytic uremic syndrome-associated variants and autoantibodies impair binding of factor h and factor h-related protein 1 to pentraxin 3.

Characterization of complement factor H-related (CFHR) proteins in plasma reveals novel genetic variations of CFHR1 associated with atypical hemolytic uremic syndrome

Complement Genetic Variants and FH Desialylation in <i>S. pneumoniae</i>-Haemolytic Uraemic Syndrome

Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significance

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

Complement mutations in diacylglycerol kinase-ε-associated atypical hemolytic uremic syndrome

Eculizumab long-term therapy for pediatric renal transplant in aHUS with CFH/CFHR1 hybrid gene

Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome

Insights into hemolytic uremic syndrome: segregation of three independent predisposition factors in a large, multiple affected pedigree

Mutations in proteins of the alternative pathway of complement and the pathogenesis of atypical hemolytic uremic syndrome

Potentiation of complement regulator factor H protects human endothelial cells from complement attack in aHUS sera

Predisposition to atypical hemolytic uremic syndrome involves the concurrence of different susceptibility alleles in the regulators of complement activation gene cluster in 1q32.

Structural and functional characterization of factor H mutations associated with atypical hemolytic uremic syndrome

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