Browsing publications by Dr David Kavanagh

Newcastle AuthorsTitleYear
Dr Edwin Wong
Holly Anderson
Rachel Challis
Dr Lisa Turnbull
Daniel Ahlert
et al.
Characterization of a Factor H Mutation That Perturbs the Alternative Pathway of Complement in a Family with Membranoproliferative GN2014
Dr David Kavanagh
Thrombotic Microangiopathy Associated with Interferon Beta2014
Rachel Challis
Holly Anderson
Dr Edwin Wong
Dr Lisa Turnbull
Dr Kevin Marchbank
et al.
Atypical haemolytic uraemic syndrome associated with a novel hybrid CFH/CFHR3 gene2013
Dr David Kavanagh
Professor Tim Goodship
Dr Anna Richards
Atypical hemolytic uremic syndrome2013
Dr Edwin Wong
Professor Tim Goodship
Dr David Kavanagh
Complement therapy in atypical haemolytic uraemic syndrome (aHUS)2013
Dr Lucy Holmes
Dr Lisa Turnbull
Dr Iain Moore
Dr Kevin Marchbank
Dr David Kavanagh
et al.
Determining the Population Frequency of the CFHR3/CFHR1 Deletion at 1q322013
Holly Anderson
Dr David Kavanagh
Rare variants in CFI, C3 and C9 are associated with high risk of advancedage-related macular degeneration.2013
Dr David Kavanagh
Dr Lisa Turnbull
Dr Kevin Marchbank
Professor Tim Goodship
A novel hybrid CFH/CFHR3 gene generated by a microhomology-mediated deletion in familial atypical hemolytic uremic syndrome2012
Professor Tim Goodship
Dr Isabel Pappworth
Dr Iain Moore
Dr Eva-Maria Hunze
James Staniforth
et al.
Factor H autoantibodies in membranoproliferative glomerulonephritis2012
Dr David Kavanagh
Dr Isabel Pappworth
Christine Hayes
Dr Iain Moore
Dr Eva-Maria Hunze
et al.
Factor I Autoantibodies in Patients with Atypical Hemolytic Uremic Syndrome: Disease-Associated or an Epiphenomenon?2012
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