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Browsing publications by Professor Tim Goodship

Newcastle AuthorsTitleYearFull text
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
Professor Tim Goodship
Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference2017
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
Dr Rebecca Darlay
Aisling Stewart
Dr Yaobo Xu
Dr Mauro Santibanez Koref
Professor John Sayer
et al.		Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux2017
Rachel Challis
Dr Edwin Wong
Dr Vicky Brocklebank
Dr Valerie Wilson
Dr 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
Professor Neil Sheerin
Professor David Kavanagh
Professor Tim Goodship
Dr Sally Johnson
A national specialised service in England for atypical haemolytic uraemic syndrome – the first year’s experience2016
Professor Tim Goodship
An unusual case of haemolytic uraemic syndrome following endoscopic retrograde cholangiopancreatography rapidly improved with eculizumab2016
Dr Valerie Wilson
Tom Cox
Dr Kate Smith-Jackson
Professor David Kavanagh
Professor Tim Goodship
et al.		Chromosomal rearrangement – a rare cause of complement factor I associated atypical haemolytic uraemic syndrome2016
Dr Veronique Fremaux-Bacchi
Professor Tim Goodship
Database of Complement Gene Variants: A comprehensive database providing insights on function, structure and allele frequency for genetic variants identified in complement-mediated diseases2016
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