List of works - Lisa Strain

A novel hybrid CFH/CFHR3 gene generated by a microhomology-mediated deletion in familial atypical hemolytic uremic syndrome

scientific article

A novel non-synonymous polymorphism (p.Arg240His) in C4b-binding protein is associated with atypical hemolytic uremic syndrome and leads to impaired alternative pathway cofactor activity

scientific article

Association of a factor H mutation with hemolytic uremic syndrome following a diarrheal illness

scientific article

Association of factor H autoantibodies with deletions of CFHR1, CFHR3, CFHR4, and with mutations in CFH, CFI, CD46, and C3 in patients with atypical hemolytic uremic syndrome

scientific article

Atypical haemolytic uraemic syndrome associated with a hybrid complement gene

scientific article (publication date: October 2006)

Atypical relapse of hemolytic uremic syndrome after transplantation

scientific article

Challenges in the management of infantile factor H associated hemolytic uremic syndrome.

scientific article

Characterization of a factor H mutation that perturbs the alternative pathway of complement in a family with membranoproliferative GN.

scientific article

Chromosomal rearrangement-A rare cause of complement factor I associated atypical haemolytic uraemic syndrome

scientific article published on 10 May 2016

Common genetic variants in complement genes other than CFH, CD46 and the CFHRs are not associated with aHUS.

scientific article

Complement factor H-associated atypical hemolytic uremic syndrome in monozygotic twins: concordant presentation, discordant response to treatment

scientific article

Complement factor h autoantibodies and age-related macular degeneration.

scientific article

De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome

scientific article

Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome

scientific article

Determining the population frequency of the CFHR3/CFHR1 deletion at 1q32.

scientific article

Factor I autoantibodies are associated with atypical haemolytic uraemic syndrome

scholarly article by David Kavanagh et al published August 2010 in Molecular Immunology

Factor I autoantibodies in patients with atypical hemolytic uremic syndrome: disease-associated or an epiphenomenon?

scientific article

Factors determining penetrance in familial atypical haemolytic uraemic syndrome

scientific article

Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome

scientific article

Posttransplantation cytomegalovirus-induced recurrence of atypical hemolytic uremic syndrome associated with a factor H mutation: successful treatment with intensive plasma exchanges and ganciclovir

scientific article

The complement factor H R1210C mutation is associated with atypical hemolytic uremic syndrome

scientific article

Thrombotic Microangiopathy in Inverted Formin 2-Mediated Renal Disease

scientific article

Triggering of atypical hemolytic uremic syndrome by influenza A (H1N1).

scientific article

List of works by Lisa Strain

A novel hybrid CFH/CFHR3 gene generated by a microhomology-mediated deletion in familial atypical hemolytic uremic syndrome

A novel non-synonymous polymorphism (p.Arg240His) in C4b-binding protein is associated with atypical hemolytic uremic syndrome and leads to impaired alternative pathway cofactor activity

Association of a factor H mutation with hemolytic uremic syndrome following a diarrheal illness

Association of factor H autoantibodies with deletions of CFHR1, CFHR3, CFHR4, and with mutations in CFH, CFI, CD46, and C3 in patients with atypical hemolytic uremic syndrome

Atypical haemolytic uraemic syndrome associated with a hybrid complement gene

Atypical relapse of hemolytic uremic syndrome after transplantation

Challenges in the management of infantile factor H associated hemolytic uremic syndrome.

Characterization of a factor H mutation that perturbs the alternative pathway of complement in a family with membranoproliferative GN.

Chromosomal rearrangement-A rare cause of complement factor I associated atypical haemolytic uraemic syndrome

Common genetic variants in complement genes other than CFH, CD46 and the CFHRs are not associated with aHUS.

Complement factor H-associated atypical hemolytic uremic syndrome in monozygotic twins: concordant presentation, discordant response to treatment

Complement factor h autoantibodies and age-related macular degeneration.

De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome

Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome

Determining the population frequency of the CFHR3/CFHR1 deletion at 1q32.

Factor I autoantibodies are associated with atypical haemolytic uraemic syndrome

Factor I autoantibodies in patients with atypical hemolytic uremic syndrome: disease-associated or an epiphenomenon?

Factors determining penetrance in familial atypical haemolytic uraemic syndrome

Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome

Posttransplantation cytomegalovirus-induced recurrence of atypical hemolytic uremic syndrome associated with a factor H mutation: successful treatment with intensive plasma exchanges and ganciclovir

The complement factor H R1210C mutation is associated with atypical hemolytic uremic syndrome

Thrombotic Microangiopathy in Inverted Formin 2-Mediated Renal Disease

Triggering of atypical hemolytic uremic syndrome by influenza A (H1N1).