Browsing publications by Dr Grainne Gorman

Newcastle AuthorsTitleYear
Dr Grainne Gorman
Dr John Grady
Dr Andrew Schaefer
Dr Richard McNally
Professor Patrick Chinnery
et al.
Mitochondrial Donation: How Many Women Could Benefit?2015
Dr Brook Galna
Jane Newman
Dr Djordje Jakovljevic
Dr Matthew Bates
Dr Andrew Schaefer
et al.
Discrete gait characteristics are associated with m.3243A > G and m.8344A > G variants of mitochondrial disease and its pathological consequences2014
Charlotte Alston
Gavin Falkous
Professor Doug Turnbull
Professor Robert Taylor
Dr Grainne Gorman
et al.
Distal weakness with respiratory insufficiency caused by the m.8344A > G "MERRF" mutation2014
Dr Gerald Pfeffer
Dr Grainne Gorman
Dr Helen Griffin
Dr Marzena Kurzawa-Akanbi
Dr Ian Wilson
et al.
Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance2014
Dr James Frith
Professor Fai Ng
Professor Chris Day
Dr Brendan Payne
Professor Neil Sheerin
et al.
Orthostatic intolerance is common in chronic disease - A clinical cohort study2014
Dr Grainne Gorman
Josh Wood
Professor Michael Trenell
Physical Activity, Exercise, and Aging2014
Professor Robert Taylor
Dr Angela Pyle
Dr Helen Griffin
Dr Jennifer Duff
Dr Langping He
et al.
Use of Whole-Exome Sequencing to Determine the Genetic Basis of Multiple Mitochondrial Respiratory Chain Complex Deficiencies2014
Dr Anna Sarkozy
Dr Debbie Hicks
Dr Steven Laval
Dr Rita Barresi
Dr Lizzie Harris
et al.
ANO5 Gene Analysis in a Large Cohort of Patients with Anoctaminopathy: Confirmation of Male Prevalence and High Occurrence of the Common Exon 5 Gene Mutation2013
Katherine Jones
Dr Roger Whittaker
Dr James Miller
Dr Djordje Jakovljevic
Professor Doug Turnbull
et al.
Can high intensity interval training improve functional capacity and clinical symptoms in inflammatory and mitochondrial myopathies?2013
Dr Matthew Bates
Dr Kieren Hollingsworth
Jane Newman
Dr Djordje Jakovljevic
Professor Andrew Blamire
et al.
Concentric hypertrophic remodeling and subendocardial dysfunction in mitochondrial DNA point mutation carriers2013
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