Browsing publications by Dr Florence Burte

Newcastle AuthorsTitleYearFull text
David Moore
Dr Florence Burte
Dr Patrick Yu Wai Man
A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca2+ homeostasis and ER-mitochondria interactions2017
David Moore
Dr Florence Burte
Dr Patrick Yu Wai Man
Corrigendum: A novel CISD2 mutation associated with a classical wolfram syndrome phenotype alters Ca21 homeostasis and ER-mitochondria interactions. [Human Molecular Genetics (2017)], doi: 10.1093/hmg/ddx0602017
Dr Patrick Yu Wai Man
David Moore
Dr Florence Burte
Evaluating the therapeutic potential of idebenone and related quinone analogues in Leber hereditary optic neuropathy2017
Dr Florence Burte
Dr Dave Houghton
Hannah Lowes
Dr Angela Pyle
Sarah Nesbitt
et al.
Metabolic profiling of Parkinson's disease and mild cognitive impairment2017
Dr Florence Burte
Dr Patrick Yu Wai Man
CHCHD10 mutations promote loss of mitochondrial cristae junctions with impaired mitochondrial genome maintenance and inhibition of apoptosis2016
Dr Patrick Yu Wai Man
Dr Florence Burte
A neurodegenerative perspective on mitochondrial optic neuropathies2016
Padraig Flannery
Dr Florence Burte
Professor Robert Taylor
Professor Laurence Bindoff
Dr Patrick Yu Wai Man
et al.
Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous OPA1 mutation2016
Dr Florence Burte
The IL17F and IL17RA Genetic Variants Increase Risk of Cerebral Malaria in Two African Populations2016
Dr Florence Burte
Professor Patrick Chinnery
Dr Patrick Yu Wai Man
Disturbed mitochondrial dynamics and neurodegenerative disorders2015
Dr Florence Burte
Malaria Induces Anemia through CD8+ T Cell-Dependent Parasite Clearance and Erythrocyte Removal in the Spleen2015
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