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Plos One|April 25, 2013
Determining the population frequency of the CFHR3/CFHR1 deletion at 1q32Lucy V Holmes, Lisa Strain, Scott J Staniforth, et al.
Current Opinion in Nephrology and Hypertension|July 10, 2002
The genetics and pathogenesis of haemolytic uraemic syndrome and thrombotic thrombocytopenic purpuraAnna Richards, Judith A Goodship, Timothy H J Goodship
Molecular Immunology|August 3, 2006
Implications of the initial mutations in membrane cofactor protein (MCP; CD46) leading to atypical hemolytic uremic syndromeAnna Richards, M Kathryn Liszewski, David Kavanagh, et al.
Immunobiology|June 9, 2016
Chromosomal rearrangement-A rare cause of complement factor I associated atypical haemolytic uraemic syndromePatrick J Gleeson, Valerie Wilson, Thomas E Cox, et al.
Journal of the American Society of Nephrology : JASN|May 27, 2005
Mutations in complement factor I predispose to development of atypical hemolytic uremic syndromeDavid Kavanagh, Elizabeth J Kemp, Elizabeth Mayland, et al.
Blood|November 8, 2011
A novel hybrid CFH/CFHR3 gene generated by a microhomology-mediated deletion in familial atypical hemolytic uremic syndromeNigel J Francis, Bairbre McNicholas, Atif Awan, et al.
Molecular Immunology|June 29, 2007
Characterization of mutations in complement factor I (CFI) associated with hemolytic uremic syndromeDavid Kavanagh, Anna Richards, Marina Noris, et al.
Clinical Kidney Journal|September 29, 2015
Use of eculizumab in crescentic IgA nephropathy: proof of principle and conundrum?Troels Ring, Birgitte Bang Pedersen, Giedrius Salkus, et al.
Human Mutation|November 11, 2005
An interactive web database of factor H-associated hemolytic uremic syndrome mutations: insights into the structural consequences of disease-associated mutationsRebecca E Saunders, Timothy H J Goodship, Peter F Zipfel, et al.
Nephron Extra|October 29, 2013
Prevalence in the General Population of a CFH Sequence Variant Associated with Atypical Haemolytic Uraemic Syndrome in an Extensive Family from Southwest EnglandAlexander J Hamilton, Carl B A Lyons, Timothy H J Goodship, et al.
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