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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
Rachel Challis
Dr Edwin Wong
Dr Vicky Brocklebank
Dr Valerie Wilson
Professor Kevin Marchbank
et al.
Thrombotic Microangiopathy in Inverted Formin 2-Mediated Renal Disease2017
Rachel Challis
Dr Edwin Wong
Dr Holly Anderson
Dr Valerie Wilson
Dr Vicky Brocklebank
et al.
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 Syndrome2016
Dr Vicky Brocklebank
Dr Edwin Wong
Professor Kevin Marchbank
Professor Tim Goodship
Professor David Kavanagh
et al.
The role of ADAMTS-13 activity and complement mutational analysis in differentiating acute thrombotic microangiopathies2016
Dr Edwin Wong
Dr Vicky Brocklebank
Professor Tim Goodship
Professor David Kavanagh
Dr Anna Richards
et al.
Characterisation of a C3 Mutation with Increased Resistance to Complement Regulation in an Individual with Recurrent C3GN in a Renel Transplant2015
Dr Mustafa Sevinc
Dr Vicky Brocklebank
Professor Tim Goodship
Professor David Kavanagh
Plasma resistant atypical hemolytic uremic syndrome associated with a CFH mutation treated with eculizumab: A case report2015
Dr Vicky Brocklebank
Dr Edwin Wong
Professor Tim Goodship
Professor David Kavanagh
Atypical haemolytic uraemic syndrome associated with a CD46 mutation triggered by Shigella flexneri2014
Dr Vicky Brocklebank
Professor David Kavanagh
Protecting the kidney from complement: atypical haemolytic uraemic syndrome2014