Dr Victoria NesbittClinical Research Associate
Lax NZ, Hepplewhite PD, Reeve AK, Nesbitt V, McFarland R, Jaros E, Taylor RW, Turnbull DM. Cerebellar Ataxia in Patients With Mitochondrial DNA Disease: A Molecular Clinicopathological Study .
Journal of Neuropathology and Experimental Neurology 2012, 71 (2), 148-161.
Bates MG, Nesbitt V, Kirk R, He L, Blakely EL, Alston CL, Brodlie M, Hasan A, Taylor RW, McFarland R. Mitochondrial respiratory chain disease in children undergoing cardiac transplantation: A prospective study .
International Journal of Cardiology 2012, 155 (2), 305–306.
Koene S, Rodenburg RJ, van der Knaap MS, Willemsen MAAP, Sperl W, Laugel V, Ostergaard E, Tarnopolsky M, Martin MA, Nesbitt V, Fletcher J, Edvardson S, Procaccio V, Slama A, van den Heuvel LPWJ, Smeitink JAM. Natural disease course and genotype-phenotype correlations in Complex I deficiency caused by nuclear gene defects: what we learned from 130 cases .
Journal of Inherited Metabolic Disease 2012, 35 (5), 737-747.
Nesbitt V, Kirkpatrick M, Pearson G, Colver A, Forsyth R. Risk and causes of death in children with a seizure disorder .
Developmental Medicine and Child Neurology 2012, 54 (7), 612-617.
Nesbitt V, Morrison PJ, Crushell E, Donnelly DE, Alston CL, He LP, Mcfarland R, Taylor RW. The clinical spectrum of the m.10191T > C mutation in complex I-deficient Leigh syndrome .
Developmental Medicine and Child Neurology 2012, 54 (6), 500-506.
Nesbitt V, Pitceathly R, Cockell S, Poulton J, Rahman S, Hanna M, Turnbull D, McFarland R. The medical research council neuromuscular centre for translational research mitochondrial disease patient cohort study UK: from conceptualisation to utilisation .
In: United Kingdom Neuromuscular Translational Research Conference . 2012, Newcastle upon Tyne: Elsevier Ltd.
Nesbitt V, Pitceathly RDS, Rahman S, Hanna MG, McFarland R, Turnbull DM. A3243G - more than just MELAS! .
In: UK Neuromuscular Translational Research Conference . 2011, London: Neuromuscular Disorders: Pergamon.
Nesbitt V, Bartlett K, Taylor RW, McFarland R. Congenital lactic acidosis and mitochondrial disease - when to suspect and how to manage .
Journal of Neonatal and Perinatal Medicine 2011, 4 (3), 179-187.
Nesbitt V, Bates MGD, Turnbull DM, McFarland R. Diabetes is a risk factor for hypertension in adults with the m.3243A > G mitochondrial DNA mutation .
In: UK Neuromuscular Translational Research Conference . 2011, London: Neuromuscular Disorders: Pergamon.
Nesbitt V, McFarland R. Diabetes is not a common feature in children with mtDNA disease .
In: UK Neuromuscular Translational Research Conference . 2011, London: Neuromuscular Disorders: Pergamon.
Nesbitt V, Whittaker R, Turnbull D, McFarland R, Taylor R. mtDNA disease for the neurologist .
Future Neurology 2011, 6 (1), 63-80.
Nesbitt V, Pitceathly RDS, Rahman S, Poulton J, Turnbull DM, Hanna MG, McFarland R. The MRC Centre for Translational Research in Neuromuscular Disease: Mitochondrial Disease Patient Cohort Study UK .
In: UK Neuromuscular Translational Research Conference . 2011, London: Neuromuscular Disorders: Pergamon.
