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Developmental Medicine and Child Neurology|April 17, 2012
Risk and causes of death in children with a seizure disorderVictoria Nesbitt, Martin Kirkpatrick, Gale Pearson, et al.JIMD Reports|September 11, 2015
Causes of Death in Adults with Mitochondrial DiseaseMarlieke Barends, Lotte Verschuren, Eva Morava, et al.Acta Paediatrica (Oslo, Norway : 1992)|January 28, 2022
Age at diagnosis, anthropometry and birthweight in two ethnically different cohorts of children with type 1 diabetes living in Northwest England or SingaporeSze May Ng, Surendran Chandrasekaran, Victoria Nesbitt, et al.Developmental Medicine and Child Neurology|February 28, 2012
The clinical spectrum of the m.10191T>C mutation in complex I-deficient Leigh syndromeVictoria Nesbitt, Patrick J Morrison, Ellen Crushell, et al.Journal of Neuropathology and Experimental Neurology|January 18, 2012
Cerebellar ataxia in patients with mitochondrial DNA disease: a molecular clinicopathological studyNichola Zoe Lax, Philippa Denis Hepplewhite, Amy Katherine Reeve, et al.Journal of Clinical Medicine|August 22, 2017
Use of FGF-21 as a Biomarker of Mitochondrial Disease in Clinical PracticeAlireza Morovat, Gayani Weerasinghe, Victoria Nesbitt, et al.Journal of Neurology, Neurosurgery, and Psychiatry|January 29, 2013
The UK MRC Mitochondrial Disease Patient Cohort Study: clinical phenotypes associated with the m.3243A>G mutation--implications for diagnosis and managementVictoria Nesbitt, Robert D S Pitceathly, Doug M Turnbull, et al.European Journal of Human Genetics : EJHG|March 20, 2014
A national perspective on prenatal testing for mitochondrial diseaseVictoria Nesbitt, Charlotte L Alston, Emma L Blakely, et al.Ophthalmology. Retina|July 14, 2021
Mitochondrial RetinopathyJohannes Birtel, Christina von Landenberg, Martin Gliem, et al.Brain : a Journal of Neurology|November 27, 2013
Disease progression in patients with single, large-scale mitochondrial DNA deletionsJohn P Grady, Georgia Campbell, Thiloka Ratnaike, et al.Pageof 2