The Wellcome Trust Centre for Mitochondrial Research is built on our long standing clinical and scientific expertise in mitochondrial disease. We are totally committed to provide the best of care for our patients. We have very close links to the NHS Highly Specialised NHS Service for Rare Mitochondrial Disorders of Adults and Children. This Clinical Service is based within the Newcastle upon Tyne Hospitals NHS Foundation Trust and provides care for patients throughout the UK both in terms of diagnosis and management. It is led by Professor Doug Turnbull for adults and Dr Robert McFarland for children. There is a diagnostic laboratory led by Professor Rob Taylor providing tests for both biochemical and genetic diagnosis. For more information please click on the links to the left.
Press the escape key to close the dialog menu.
Menu
- Menu
- Search
- News & Events
Tabs in this tab group open the tab panel widget in a dialog. Once a tab is interacted with, press the escape key to exit the dialog and return to the page content.
- Home
- Coronavirus Advice
- Coronavirus: latest government advice on shielding
- Coronavirus: latest psychology update
- Coronavirus: psychology update for Mental Health Awareness Week
- Coronavirus: psychology update
- Coronavirus: latest psychology advice
- Coronavirus: psychology update
- Coronavirus: latest psychological advice for patients and families
- Coronavirus: latest psychological advice (FACE COVID)
- Coronavirus: Mental Health and Well-being
- Our Science Home Page
- Patient And Public
- What are mitochondria?
- About Our Clinic
- General information about mitochondrial disease
- Mitochondrial Reproductive Options
- Specific conditions
- Large-scale mitochondrial DNA deletions
- Neurogenic weakness, Ataxia, and Retinitis Pigmentosa (NARP)
- Multiple mitochondrial DNA deletions
- Mitochondrial Neuro-gastro-intestinal encephalopathy (MNGIE)
- Myoclonic Epilepsy and Ragged Red Fibres (MERRF 8344 A>G)
- Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis and Stroke-Like Episodes (MELAS) 3243 A>G mutation
- Leigh syndrome
- Mitochondrial DNA depletion syndrome (MDDS)
- Alpers’ syndrome
- Our Patient Days
- Mitonews
- Fundraising
- Clinical Professionals
- Clinical Guidelines
- Mitochondrial Patient Cohort
- Engagement
- Team members
- Principal Investigators
- Professor Zofia Chrzanowska-Lightowlers
- Dr Grainne Gorman
- Dr Laura Greaves
- Dr Gavin Hudson
- Professor Mary Herbert
- Professor Robert Lightowlers
- Professor Robert McFarland
- Dr Brendan Payne
- Prof Robert Taylor
- Prof Sir Doug Turnbull
- Dr Tom Nicholls
- Dr Amy Reeve
- Dr Oliver Russell
- Dr Amy Vincent
- Dr Sarah Pickett
- Dr Yi Shiau Ng
- Dr Charlotte Alston
- Post Doctoral Scientists
- Clinical Team Members
- Associated Researchers
- NHS Diagnostic Laboratory Team Members
- Post Graduate Students
- Administrative and Technical
- Principal Investigators
- WCMR Seminars
- Contact Us
