Victoria Nesbitt
Oxford, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 23 publications
Autosomal dominant HK1-related neurodevelopmental disorder with visual defects and brain anomalies (NEDVIBA): An emerging mitochondrial disorder.
Journal: Genetics in medicine open
Published: April 06, 2024
Deoxyguanosine kinase deficiency: natural history and liver transplant outcome.
Journal: Brain communications
Published: November 29, 2023
Digenic Leigh syndrome on the background of the m.11778G>A Leber hereditary optic neuropathy variant.
Journal: Brain : a journal of neurology
Published: August 09, 2023
Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study.
Journal: BMJ (Clinical research ed.)
Published: November 04, 2021
Age at diagnosis, anthropometry and birthweight in two ethnically different cohorts of children with type 1 diabetes living in Northwest England or Singapore.
Journal: Acta paediatrica (Oslo, Norway : 1992)
Published: November 02, 2021
Forecasting stroke-like episodes and outcomes in mitochondrial disease.
Journal: Brain : a journal of neurology
Published: May 10, 2021
Natural History of Leigh Syndrome: A Study of Disease Burden and Progression.
Journal: Annals of neurology
Published: March 31, 2021
Consensus-based statements for the management of mitochondrial stroke-like episodes.
Journal: Wellcome open research
Published: December 06, 2019
A case-comparison study of pregnant women with mitochondrial disease - what to expect?
Journal: BJOG : an international journal of obstetrics and gynaecology
Published: February 19, 2019
Pathogenic variants in MT-ATP6: A United Kingdom-based mitochondrial disease cohort study.
Journal: Annals of neurology
Published: January 18, 2019
Diagnosis of 'possible' mitochondrial disease: an existential crisis.
Journal: Journal of medical genetics
Published: October 12, 2018
Last Updated: 09/26/2026