Dr Hannah Steele Dr Angela Pyle Sila Hopton Jane Newman Dr Renae Stefanetti et al. | Metabolic effects of bezafibrate in mitochondrial disease. | 2020 |
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Dr Boglárka Bánsági Dr Helen Griffin Professor Roger Whittaker Dr Teresinha Evangelista Dr James Miller et al. | Genetic heterogeneity of motor neuropathies | 2017 |
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Dr Hannah Steele Professor Rita Horvath Professor Patrick Chinnery
| Monitoring clinical progression with mitochondrial disease biomarkers | 2017 |
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Dr Michael Keogh Dr Stephan Jaiser Dr Hannah Steele Professor Rita Horvath Professor Patrick Chinnery et al. | PLP1 mutations and central demyelination: evidence from electrophysiologic phenotyping in female manifesting carriers | 2017 |
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Dr Hannah Steele Dr Angela Pyle Dr Yvonne Hart Dr Richard Quinton Professor Patrick Chinnery et al. | A Woman With Intellectual Disability, Amenorrhoea, Seizures, and Balance Problems | 2016 |
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Dr Hannah Steele Dr Lizzie Harris Dr Rita Barresi Dr John Bourke Professor Volker Straub et al. | Cardiac involvement in hereditary myopathy with early respiratory failure: A cohort study | 2016 |
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Dr Hannah Steele Professor Rita Horvath Professor Robert Taylor
| The swinging pendulum of biomarkers in mitochondrial disease: the role of FGF21 | 2016 |
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Dr Michael Keogh Daniyal Daud Dr Angela Pyle Dr Jennifer Duff Dr Helen Griffin et al. | A novel de novo STXBP1 mutation is associated with mitochondrial complex I deficiency and late-onset juvenile-onset parkinsonism | 2015 |
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Dr Michael Keogh Dr Hannah Steele Dr Konstantinos Douroudis Dr Angela Pyle Dr Jennifer Duff et al. | Frequency of rare recessive mutations in unexplained late onset cerebellar ataxia | 2015 |
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Dr Hannah Steele Professor Patrick Chinnery
| Mitochondrial Causes of Epilepsy: Evaluation, Diagnosis, and Treatment | 2015 |
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Dr Hannah Steele Dr Anna Basu Professor Patrick Chinnery
| The Eye of the Tiger with Night Blindness: Retinitis Pigmentosa as a presenting feature of PKAN | 2015 |
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