List of works - Pilar Sánchez-Corral

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

scientific article

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

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

scientific article

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

scientific article

Atypical aHUS: State of the art.

scientific article

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

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

Complement mutations in diacylglycerol kinase-ε-associated 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

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

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

scientific article

Early treatment with eculizumab in atypical haemolytic uraemic syndrome

scientific article published on January 31, 2012

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

scientific article

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

scientific article published on 15 March 2012

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

scientific article published on 01 February 2019

Complement Genetic Variants and FH Desialylation in S. pneumoniae-Haemolytic Uraemic Syndrome

scientific article published on 11 March 2021

List of works by Pilar Sánchez-Corral

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

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

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

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

Atypical aHUS: State of the art.

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

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

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

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

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

Early treatment with eculizumab in atypical haemolytic uraemic syndrome

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

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

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

Complement Genetic Variants and FH Desialylation in S. pneumoniae-Haemolytic Uraemic Syndrome