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Browsing publications by Dr Valerie Wilson

Newcastle AuthorsTitleYearFull text
Emily Glover
Dr Kate Smith-Jackson
Dr Vicky Brocklebank
Dr Valerie Wilson
Dr Patrick Walsh
et al.		Assessing the Impact of Prophylactic Eculizumab on Renal Graft Survival in Atypical Hemolytic Uremic Syndrome2023
Dr Vicky Brocklebank
Dr Patrick Walsh
Dr Kate Smith-Jackson
Dr Thomas Hallam
Professor Kevin Marchbank
et al.		Atypical haemolytic uraemic syndrome in the era of terminal complement inhibition- An observational cohort study2023
Dr Ruth Richardson
Dr Valerie Wilson
Dr Michael Wright
Further delineation of phenotypic spectrum of SCN2A-related disorder2022
Professor Kevin Marchbank
Dr Isabel Pappworth
Harriet Denton
Kate Cooke
Grant Richardson
et al.		C3 Glomerulopathy and Related Disorders in Children.2021
Dr Valerie Wilson
Professor Sir John Burn
Dr Akhtar Husain
Professor Neil Rajan
Detection of genetic tumour predisposition syndromes using electronic health records2020
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 Majid Arefi
Dr Valerie Wilson
Dr Siobhan Muthiah
Dr Simon Zwolinski
Dr Dalvir Bajwa
et al.		Diverse presentations of cutaneous mosaicism occur in CYLD cutaneous syndrome and may result in parent-to-child transmission2019
Professor David Kavanagh
Dr Valerie Wilson
Professor Tim Goodship
Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy2018
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 Valerie Wilson
Tom Cox
Dr Kate Smith-Jackson
Professor David Kavanagh
Professor Tim Goodship
Chromosomal rearrangement – a rare cause of complement factor I associated atypical haemolytic uraemic syndrome2016
Dr Valerie Wilson
Dr David Bourn
Professor Neil Rajan
CYLD Genetic Testing for Brooke-Spiegler Syndrome, Familial Cylindromatosis and Multiple Familial Trichoepitheliomas2015
Dr Valerie Wilson
Professor Tim Goodship
Dr Veronique Fremaux-Bacchi
Mapping interactions between complement C3 and regulators using mutations in atypical hemolytic uremic syndrome2015
Professor Heather Cordell
Dr Valerie Wilson
Professor Judith Goodship
Professor Tim Goodship
Factors determining penetrance in familial atypical haemolytic uraemic syndrome2014
Dr Valerie Wilson
Dr Rebecca Darlay
Dr Katrina Wood
Professor Claire Harris
Dr Eva-Maria Hunze
et al.		Genotype/Phenotype Correlations in Complement Factor H Deficiency Arising From Uniparental Isodisomy2013
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