Browsing publications by Christine Hayes

Newcastle AuthorsTitleYear
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
Christine Hayes
Sonia Bussey
Podiatric Medicine Unravelled2011
Dr Isabel Pappworth
Christine Hayes
Dr Andrew Knight
Dr Kevin Marchbank
The role of complement in the formation of B regulatory cells2010
Professor Robert Taylor
Dr Andrew Schaefer
Christine Hayes
Dr Bobby McFarland
Professor Doug Turnbull
et al.
Catastrophic presentation of mitochondrial disease due to a mutation in the tRNAHis gene2004
Dr Bobby McFarland
Dr Andrew Schaefer
Dr Julie Murphy
Dr Stephen Lynn
Christine Hayes
et al.
Familial Myopathy: New Insights into the T14709C Mitochondrial tRNA Mutation2004
Professor Robert Taylor
Dr Hugh Bain
Christine Hayes
Dr Martin Barron
Professor Robert Lightowlers
et al.
A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy2003
Dr Andrew Schaefer
Dr Bobby McFarland
Dr Julie Murphy
Dr Stephen Lynn
Christine Hayes
et al.
Familial mitochondrial myopathy: New insights into the T14709C mitochondrial tRNA mutation2003
Professor Robert Taylor
Christine Hayes
Mary Johnson
Professor Katherine Bushby
Professor Doug Turnbull
et al.
Investigation of mitochondrial function in hereditary spastic paraparesis2002
Professor Robert Taylor
Christine Hayes
Professor Doug Turnbull
Molecular and functional effects of the T14709C point mutation in the mitochondrial DNA of a patient with maternally inherited diabetes and deafness2002
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