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Browsing publications by Dr Vicky Brocklebank

Newcastle AuthorsTitleYearFull text
Dr Edwin Wong
Thomas Hallam
Dr Vicky Brocklebank
Dr Patrick Walsh
Dr Kate Smith-Jackson
et al.
Functional characterisation of rare genetic variants in the N-terminus of complement factor H in aHUS, C3G and AMD2021
Tom Hallam
Professor Claire Harris
Nik Tzoumas
David Steel
Victoria Shuttleworth
et al.
The Rare C9 P167S Risk Variant for Age-related Macular Degeneration Increases Polymerization of the Terminal Component of the Complement Cascade.2021
Dr Vicky Brocklebank
Dr Kate Smith-Jackson
Dr Patrick Walsh
Professor Kevin Marchbank
Professor Claire Harris
et al.
Long-term outcomes and response to treatment in DGKE nephropathy2020
Dr Christopher Duncan
Dr Benjamin Thompson
Dr Rui Chen
Dr Florian Gothe
Victoria Shuttleworth
et al.
Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in STAT22019
Dr Patrick Walsh
Dr Sally Johnson
Dr Vicky Brocklebank
Dr Jacobo Salvatore
Professor David Kavanagh
et al.
Glucose-6-Phosphate Dehydrogenase Deficiency Mimicking Atypical Hemolytic Uremic Syndrome2018
Dr Vicky Brocklebank
Dr Katrina Wood
Professor David Kavanagh
Thrombotic microangiopathy and the kidney2018
Dr Vicky Brocklebank
Professor David Kavanagh
Complement C5-inhibiting therapy for the thrombotic microangiopathies: accumulating evidence, but not a panacea2017
Dr Vicky Brocklebank
Dr Sally Johnson
Dr Patrick Walsh
Dr Edwin Wong
Dr Larissa Kerecuk
et al.
Factor H autoantibody is associated with atypical hemolytic uremic syndrome in children in the United Kingdom and Ireland2017
Professor David Kavanagh
Dr Edwin Wong
Dr Vicky Brocklebank
Hemolytic Uremic Syndrome in Pregnancy and Post-Partum2017
Dr Katrina Wood
Dr Alison Brown
Professor David Kavanagh
Dr Vicky Brocklebank
Rare genetic variants in Shiga toxin–associated haemolytic uraemic syndrome: genetic analysis prior to transplantation is essential2017
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