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Browsing publications by Joanna Stewart.

Newcastle AuthorsTitleYearFull text
Kamil Sitarz
Dr Patrick Yu Wai Man
Dr Angela Pyle
Joanna Stewart
Professor Rita Horvath
et al.
MFN2 mutations cause compensatory mitochondrial DNA proliferation2012
Dr Kamil Sitarz
Dr Patrick Yu Wai Man
Dr Angela Pyle
Joanna Stewart
Professor Rita Horvath
et al.
MFN2 mutations cause compensatory mitochondrial DNA proliferation2012
Joanna Stewart
Kamil Sitarz
Professor Rita Horvath
Dr Angela Pyle
Dr Patrick Yu Wai Man
et al.
POLG mutations cause decreased mitochondrial DNA repopulation rates following induced depletion in human fibroblasts2011
Joanna Stewart
Professor Gavin Hudson
Professor Hanns Lochmuller
Professor Patrick Chinnery
Professor Rita Horvath
et al.
Late-onset ptosis and myopathy in a patient with a heterozygous insertion in POLG22010
Joanna Stewart
Professor Rita Horvath
Professor Chris Day
Professor Patrick Chinnery
Polymerase γ Gene POLG Determines the Risk of Sodium Valproate-Induced Liver Toxicity2010
Professor Grainne Gorman
Joanna Stewart
Dr Mark Buddles
Professor Patrick Chinnery
Emeritus Professor Doug Turnbull
et al.
Autosomal dominant Progressive External Ophthalmoplegia (adPEO) due to mutations in the PEO1 gene: A clinical, histochemical and molecular survey of 33 patients2009
Joanna Stewart
Professor Rita Horvath
Professor Patrick Chinnery
Common POLG Genetic Variants Increase the Risk of Sodium Valproate Induced Liver Injury and Failure2009
Joanna Stewart
Professor Patrick Chinnery
Professor Hanns Lochmuller
Professor Rita Horvath
In vitro supplementation with dAMP/dGMP leads to partial restoration of mtDNA levels in mitochondrial depletion syndromes2009
Joanna Stewart
Professor Gavin Hudson
Dr Patrick Yu Wai Man
Professor Rita Horvath
Philip Griffiths
et al.
OPA1 in multiple mitochondrial DNA deletion disorders2008
Joanna Stewart
Professor Robert Taylor
Professor Patrick Chinnery
Clonally expanded mitochondrial DNA mutations in epileptic individuals with mutated DNA polymerase gamma2008
Joanna Stewart
Professor Gavin Hudson
Professor Robert Taylor
Professor Patrick Chinnery
Mutations in POLG1 can present with autosomal recessive axonal Charcot-Marie-Tooth disease2008
Joanna Stewart
Dr Angela Pyle
Emeritus Professor Mike Sir Michael Rawlins
Professor Gavin Hudson
Dr Andrew Morris
et al.
Novel POLG1 mutations associated with neuromuscular and liver phenotypes in adults and children.2008
Joanna Stewart
Professor Gavin Hudson
Professor Robert Taylor
Professor Patrick Chinnery
POLG1 mutations manifesting as autosomal recessive axonal Charcot-Marie-Tooth disease2008
Joanna Stewart
A paediatric case of a solitary fibrous tumour of the parotid gland2004