Lisa Strain

Newcastle Upon Tyne, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 12 publications

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

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

Journal: Immunobiology

Published: February 24, 2016

Thrombotic Microangiopathy in Inverted Formin 2-Mediated Renal Disease.

Thrombotic Microangiopathy in Inverted Formin 2-Mediated Renal Disease.

Journal: Journal of the American Society of Nephrology : JASN

Published: October 30, 2015

Exome Sequencing of an Adult Pituitary Atypical Teratoid Rhabdoid Tumor.

Exome Sequencing of an Adult Pituitary Atypical Teratoid Rhabdoid Tumor.

Journal: Frontiers in oncology

Published: July 28, 2015

A De Novo Deletion in the Regulators of Complement Activation Cluster Producing a Hybrid Complement Factor H/Complement Factor H-Related 3 Gene in Atypical Hemolytic Uremic Syndrome.

A De Novo Deletion in the Regulators of Complement Activation Cluster Producing a Hybrid Complement Factor H/Complement Factor H-Related 3 Gene in Atypical Hemolytic Uremic Syndrome.

Journal: Journal of the American Society of Nephrology : JASN

Published: January 27, 2015

Factors determining penetrance in familial atypical haemolytic uraemic syndrome.

Factors determining penetrance in familial atypical haemolytic uraemic syndrome.

Journal: Journal of medical genetics

Published: September 28, 2014

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

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

Journal: Journal of the American Society of Nephrology : JASN

Published: April 12, 2014

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

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

Journal: PloS one

Published: November 14, 2012

Postpartum aHUS secondary to a genetic abnormality in factor H acquired through liver transplantation.

Postpartum aHUS secondary to a genetic abnormality in factor H acquired through liver transplantation.

Journal: American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons

Published: March 17, 2012

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

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

Journal: Clinical journal of the American Society of Nephrology : CJASN

Published: January 07, 2012

Factor H autoantibodies in membranoproliferative glomerulonephritis.

Factor H autoantibodies in membranoproliferative glomerulonephritis.

Journal: Molecular immunology

Published: January 05, 2012

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

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

Journal: Molecular immunology

Published: November 08, 2011

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

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

Journal: Blood

Published: November 08, 2011

Showing 1-12 of 12

Last Updated: 09/26/2026