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- Mitochondrial diseases in adults clinical study day
- Seminar: signalling pathways that control muscle mass, metabolism and longevity
- Seminar: Duchenne muscular dystrophy (DMD): a developmental disease
- MDUK Oxford Neuromuscular Centre Annual Meeting
- Seminar: Modeling muscle disease and regeneration in zebrafish - CANCELLED
- Online Seminar: Modeling muscle disease and regeneration in zebrafish
- Online Seminar: From Ion Channel Gating Pore Currents to International Genomic Medicine Initiatives in Neuromuscular Diseases
- Online Seminar: Digenic inheritance involving a muscle specific protein kinase and the giant titin protein causes a skeletal muscle myopathy
- Online Seminar: Optimizing therapeutic efficacy in spinal muscular atrophy
- Online Seminar: Therapy Development for Duchene Muscular Dystrophy: A long and winding road
- Online Seminar: Engineering human stem cells for muscle disease modelling and therapy development
- Online Seminar: Optimizing antisense mediated exon skipping for Duchenne muscular dystrophy and ultrarare diseases
- From gene to therapy for Duchenne muscular dystrophy
- Online Seminar: Myositis- morphology and molecular studies
- Online Seminar: Tricyclo-DNA: promising antisense oligonucleotides for the treatment of neuromuscular diseases
- Online Seminar: The Origin of Mitochondrial Diseases
- Quiz Fundraiser Night for MDUK Town and Gown
- Online Seminar: Diagnostic delay in Duchenne muscular dystrophy and the case for newborn screening
- Seminar: Distal myopathies – elucidation of mechanism and development of therapy
- Quiz Fundraiser Night for MDUK Town and Gown
- Bake Sale for MDUK Town and Gown
- Seminar: Protecting motor neurons from degeneration by targeting bioenergetics
- Seminar: Curbing mitochondrial dysfunction in neurodegeneration: lessons from neurogenetics
- Seminar: Emerging Oligonucleotide Therapeutics for Neuromuscular Diseases
- 2023 Annual Meeting - Register now!
- Seminar: Stem cells to treat muscular dystrophies
- Seminar: Sugars & proteins
- Seminar: Congenital disorders of autophagy and intracellular trafficking – a novel class of neurometabolic disorders linking aberrant neurodevelopment and neurodegeneration
- CANCELLED - WILL BE RESCHEDULED - Seminar: Mitochondrial DNA Disorders: the (long and winding) road to treatment
- Seminar: Wearables in mega-scale biobanks – are there some learnings for rare disease research?
- Seminar: Bridging the divide: translational research with a canine model of Duchenne Muscular Dystrophy
- MDUK Oxford Neuromuscular Centre Networking Session
- Seminar: Curating clinical science: the future of academic publishing
- A new research centre tackles neuromuscular diseases
- First steps towards treating myotonic dystrophy type 1
- NHS England to fund Spinraza drug, treating children with Spinal Muscular Atrophy
- MDUK Oxford Neuromuscular Centre researchers fundraise for MDUK
- Bake Sale for MDUK Oxford Town and Gown Support
- World-leading neurologist appointed to Professorship at MDUK Oxford Neuromuscular Centre
- MDUK-Oxford University partnership
- Two MDUK ONMC professors honoured by the Academy of Medical Sciences
- MDUK ONMC Professor, Angela Russell, awarded the 2021 Harrington UK Rare Disease Scholar Award
- The MDUK Oxford Neuromuscular Centre's First Annual Scientific Meeting
- University spinout PepGen awarded major financing to target Duchenne muscular dystrophy
- Why we must expand newborn screening
- Not a tea lady: The prime of Professor Dame Kay Davies
- Promising discovery for treatment of neuromuscular diseases
- The Duchenne Research Relay Team prove that ‘where there’s a Will, there’s a way’
- MDUK ONMC Town and Gown Team smashes fundraising target
- An opportunity for a physiotherapist to work with our team!
- Angelman syndrome: first patient to receive potential therapy in Oxford
- First UK pilot study of newborn screening for spinal muscular atrophy (SMA) launched in Oxford.
- A simple test at birth could positively transform the life of 70 families per year in the UK and save the NHS £280 every minute.
- Funding received for research into Motor Neuron Disease
- Ancient gene mutation found to cause rare hereditary condition
- Seminar Summary: Unravelling the inflammatory neuropathies
- Russell group research reveals molecular target of the Utrophin modulator Ezutromid
- Watch Kay Davies explore the latest promising genetic approaches for the diagnosis and treatment of Duchenne Muscular Dystrophy
- MDUK ONMC hits 2023 Town & Gown Fundraising target