| Phrase | Consultant | Town | Special Interests |
| Assessing cognition in patients with mitochondrial disease | *Consultant(s)* | *Towns* | Assessing cognition in patients with mitochondrial disease |
| maternally inherited mitochondrial DNA mutations | *Consultant(s)* | *Towns* | Neonatal medicine, maternally inherited mitochondrial DNA mutations |
| mitochondrial disease | *Consultant(s)* | *Towns* | Paediatric neurology, mitochondrial disease |
| Mitochondrial disease | *Consultant(s)* | *Towns* | Mitochondrial disease, neuromuscular junction disorders |
| mitochondrial disorders | *Consultant(s)* | *Towns* | Paediatric neuropathy, mitochondrial disorders, idiopathic intracranial hypertension, neurofibromatosis type 1, neuromuscular disorders, opsoclonus myoclonus |
| Mitochondrial disorders | *Consultant(s)* | *Towns* | Mitochondrial disorders, inherited metabolic diseases |
| mitochondrial disorders | *Consultant(s)* | *Towns* | Parkinson's disease, migraine, degenerative disorders, movement disorders, mitochondrial disorders, restless legs syndrome |
| Mitochondrial DNA diseases | *Consultant(s)* | *Towns* | Mitochondrial DNA diseases, genetics |
| mitochondrial dysfunction in critically ill patients | *Consultant(s)* | *Towns* | Paediatric intensive care, mitochondrial dysfunction in critically ill patients, multi-organ dysfunction |
| mitochondrial eye diseases | *Consultant(s)* | *Towns* | Neuro-ophthalmology, neurogenetics, inherited eye diseases, mitochondrial eye diseases |
| mitochondrial genetics and sepsis | *Consultant(s)* | *Towns* | Upper gastrointestinal anaesthesia, mitochondrial genetics and sepsis |
| Rare mitochondrial disease | *Consultant(s)* | *Towns* | Rare mitochondrial disease, neurogenetics, muscle disease |
| Rare mitochondrial disorders | *Consultant(s)* | *Towns* | Rare mitochondrial disorders |
