Browsing publications by Dr Grainne Gorman

Newcastle AuthorsTitleYear
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
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 Grainne Gorman
Josh Wood
Professor Michael Trenell
Physical Activity, Exercise, and Aging2014
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
Dr Matthew Bates
Jane Newman
Dr Djordje Jakovljevic
Dr Kieren Hollingsworth
Professor Andrew Blamire
et al.
Defining cardiac adaptations and safety of endurance training in patients with m.3243A>g-related mitochondrial disease2013
John Grady
Georgia Campbell
Gavin Falkous
Dr Victoria Nesbitt
Dr Andrew Schaefer
et al.
Disease progression in patients with single, large-scale mitochondrial DNA deletions2013
Jane Newman
Dr Brook Galna
Dr Djordje Jakovljevic
Dr Matthew Bates
Dr Andrew Schaefer
et al.
Evaluation of Functional Outcome Measures as a Surrogate Marker of Disease Severity in Patients with Mitochondrial Disease2013
Dr Joanna Elson
Mark Cadogan
Dr Roger Whittaker
Professor Michael Trenell
Professor Rita Horvath
et al.
Initial development and validation of a mitochondrial disease quality of life scale2013
Charlotte Alston
Dr Andrew Schaefer
Kim Krishnan
Dr Langping He
Kate Craig
et al.
Late-Onset Respiratory Failure Due to Tk2 Mutations Causing Multiple MtDNA Deletions2013
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