Publications by Dr Vicky Brocklebank - ePrints

Browsing publications by Dr Vicky Brocklebank.

Newcastle Authors	Title	Year
Dr Thomas Hallam Tom Cox Dr Kate Smith-Jackson Dr Vicky Brocklebank April Baral et al.	A novel method for real-time analysis of the complement C3b:FH:FI complex reveals dominant negative CFI variants in Age-related Macular Degeneration	2022
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 AMD	2021
Tom Hallam Gladys - 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 nephropathy	2020
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 STAT2	2019
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 Syndrome	2018
Dr Vicky Brocklebank Dr Katrina Wood Professor David Kavanagh	Thrombotic microangiopathy and the kidney	2018
Dr Vicky Brocklebank Professor David Kavanagh	Complement C5-inhibiting therapy for the thrombotic microangiopathies: accumulating evidence, but not a panacea	2017
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 Ireland	2017
Professor David Kavanagh Dr Edwin Wong Dr Vicky Brocklebank	Hemolytic Uremic Syndrome in Pregnancy and Post-Partum	2017
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 essential	2017
Rachel Challis Dr Edwin Wong Dr Vicky Brocklebank Dr Valerie Wilson Professor Kevin Marchbank et al.	Thrombotic Microangiopathy in Inverted Formin 2-Mediated Renal Disease	2017
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 Syndrome	2016
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 microangiopathies	2016
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 Transplant	2015
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 report	2015
Dr Vicky Brocklebank Dr Edwin Wong Professor Tim Goodship Professor David Kavanagh	Atypical haemolytic uraemic syndrome associated with a CD46 mutation triggered by Shigella flexneri	2014
Dr Vicky Brocklebank Professor David Kavanagh	Protecting the kidney from complement: atypical haemolytic uraemic syndrome	2014