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  • Home
  • Patient and Public
    • What are mitochondria?
    • Engagement
    • Coronavirus
    • About Our Clinic
    • General information about mitochondrial disease
    • Specific conditions
    • Mitochondrial Reproductive Options
    • Mitochondrial Patient Cohort
    • Our Patient Days
    • WCMR Seminars
    • Mitonews
    • Fundraising
  • Research
    • Clinical Research
    • Mitochondrial Gene Expression
    • Preventing Mitochondrial disease transmission
    • Mitochondria In Common Disease
    • Young Scientists
    • Career support
  • Clinical
    • Clinical Guidelines
    • Clinical Services
    • Diagnostic Laboratory
    • m.3243A>G Heteroplasmy Tool
    • Exercise Training in Neuromuscular Disorders Outcome Measures Database
    • Newcastle Mitochondrial Disease Scale for Adults
  • Clinical Trials
  • Team members
    • Principal Investigators
    • Post Doctoral Scientists
    • Clinical Team
    • Clinical Research Team
    • Associated Researchers
    • NHS Diagnostic Laboratory Team
    • Post Graduate Students
    • Administrative and Technical Team
  • News
  • Contact
  • All Trials
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  • Completed
Find

A new non-invasive diagnostic method for detection of pathogenic mitochondrial DNA variants using faecal-derived DNA samples

MDP

Muscle disease progression in mitochondrial DNA deletions

LION

Leigh syndrome: Investigating Outcome measures & Natural history - a prospective, longitudinal cohort study

Facial Imaging

Interrogating mitochondrial dysfunction in facial appearance and ageing

Mito Ataxia

Understanding and Investigating Cerebellar Ataxia in Adult Mitochondrial Disease

White Blood Cell

Predicting the progression of m.3243A>G-related mitochondrial disease using white blood cell heteroplasmy

PET MRI

Development of PET-MRS methodology for neurodegenerative diseases v7

PDH Study

Natural History Study of Pyruvate Dehydrogenase Deficiency

Wellcome Centre for Mitochondrial Research Patient Cohort

A Natural History Study and Patient Registry

The Newcastle Mitochondrial Research Biobank
Auditory Study

Evaluating auditory and vestibular dysfunction in mitochondrial patients harbouring the m.3243A>G mutation

Bladder Study

Bladder Dysfunction in Patients with Mitochondrial Disease

Prefer (Quantitative Phase)

Quantifying patient preferences in neuromuscular disorders.

Prefer (Qualitative Phase)

PREFER project case study: Patient and caregiver unmet health priorities and risk tolerance for neuromuscular treatments (qualitative phase).

Low Residue Diet

Phase II feasibility study of the efficacy and acceptability of a low residue diet in adult patients with mitochondrial disease

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