Publications by Dr Victoria Nesbitt - ePrints

Browsing publications by Dr Victoria Nesbitt.

Newcastle Authors	Title	Year
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