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Browsing publications by
Dr Victoria Nesbitt.
Newcastle Authors
Title
Year
Full text
Dr Yi Ng
Dr Nichola Lax
Dr Alasdair Blain
Dr Daniel Erskine
Professor Mark Baker
et al.
Forecasting stroke-like episodes and outcomes in mitochondrial disease
2022
Professor Rita Horvath
Dr Wei Wei
Dr Robert Pitceathly
Professor Michael Hanna
Professor John Sayer
et al.
Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: Cohort study
2021
Professor Patrick Chinnery
Professor Rita Horvath
Professor Bobby McFarland
Dr Victoria Nesbitt
Dr Hannah Steele
et al.
Diagnosis of 'possible' mitochondrial disease: an existential crisis
2019
Dr Yi Ng
Dr Mika Martikainen
Professor Grainne Gorman
Dr Alasdair Blain
Dr Andrew Schaefer
et al.
Pathogenic variants in MT-ATP6: A United Kingdom–based mitochondrial disease cohort study
2019
Professor Roger Whittaker
Professor Grainne Gorman
Dr Andrew Schaefer
Professor Rita Horvath
Dr Yi Ng
et al.
Epilepsy in Adults With Mitochondrial Disease: A Cohort Study
2015
Dr Victoria Nesbitt
Dr Robert Pitceathly
Emeritus Professor Doug Turnbull
Professor Robert Taylor
Professor Bobby McFarland
et al.
The UK MRC Mitochondrial Disease Patient Cohort Study: clinical phenotypes associated with the m.3243A>G mutation—implications for diagnosis and management
2013
Dr Nichola Lax
Philippa Hepplewhite
Dr Amy Reeve
Dr Victoria Nesbitt
Professor Bobby McFarland
et al.
Cerebellar Ataxia in Patients With Mitochondrial DNA Disease: A Molecular Clinicopathological Study
2012
Dr Matt Bates
Dr Victoria Nesbitt
Dr Langping He
Dr Charlotte Alston
Dr Malcolm Brodlie
et al.
Mitochondrial respiratory chain disease in children undergoing cardiac transplantation: A prospective study
2012
Dr Victoria Nesbitt
Natural disease course and genotype-phenotype correlations in Complex I deficiency caused by nuclear gene defects: what we learned from 130 cases
2012
Dr Victoria Nesbitt
Emeritus Professor Allan Colver
Dr Rob Forsyth
Risk and causes of death in children with a seizure disorder
2012
Dr Victoria Nesbitt
Dr Charlotte Alston
Professor Bobby McFarland
Professor Robert Taylor
The clinical spectrum of the m.10191T > C mutation in complex I-deficient Leigh syndrome
2012
Dr Victoria Nesbitt
Dr Robert Pitceathly
Dr Simon Cockell
Professor Michael Hanna
Emeritus Professor Doug Turnbull
et al.
The medical research council neuromuscular centre for translational research mitochondrial disease patient cohort study UK: from conceptualisation to utilisation
2012
Dr Victoria Nesbitt
Dr Robert Pitceathly
Professor Bobby McFarland
Emeritus Professor Doug Turnbull
A3243G - more than just MELAS!
2011
Dr Victoria Nesbitt
Professor Kim Bartlett
Professor Robert Taylor
Professor Bobby McFarland
Congenital lactic acidosis and mitochondrial disease - when to suspect and how to manage
2011
Dr Victoria Nesbitt
Dr Matt Bates
Emeritus Professor Doug Turnbull
Professor Bobby McFarland
Diabetes is a risk factor for hypertension in adults with the m.3243A > G mitochondrial DNA mutation
2011
Dr Victoria Nesbitt
Professor Bobby McFarland
Diabetes is not a common feature in children with mtDNA disease
2011
Dr Victoria Nesbitt
Professor Roger Whittaker
Emeritus Professor Doug Turnbull
Professor Bobby McFarland
Professor Robert Taylor
et al.
mtDNA disease for the neurologist
2011
Dr Victoria Nesbitt
Dr Robert Pitceathly
Emeritus Professor Doug Turnbull
Professor Bobby McFarland
The MRC Centre for Translational Research in Neuromuscular Disease: Mitochondrial Disease Patient Cohort Study UK
2011
Dr Robert Pitceathly
Dr Victoria Nesbitt
Professor Bobby McFarland
Emeritus Professor Doug Turnbull
MRC mitochondrial cohort study: development of a UK database
2010