Launched in November 2014, the Centre brings together and consolidates Newcastle's distinguished, international and world-leading record in research and care for neuromuscular diseases.
Our team, based at the Institute of Translational and Clinical Research, Newcastle University, and its associated hospitals, work together towards the development and application of genomic and translational medicine to improve the health outcomes of people living with neuromuscular diseases.
As a group we have developed a close and important link between research and clinical activities, and we actively pursue new partnerships with other stakeholders such as patient organisations, regulators and pharma.
The John Walton Muscular Dystrophy Research Centre (JWMDRC) is structured around four important Strands of activity; Clinical Care & Diagnostics, Clinical Research, Laboratory Research and Networking & Collaborations. All are strongly interlinked and the work across these teams is key to our success and impact in the neuromuscular field.
We are immensely proud to have continued to build, shape and develop this Centre's team of international experts and to be leading them now under the auspicious name of Lord John Walton, who first established a dedicated and integrated neuromuscular clinical and research unit at Newcastle Upon Tyne in the 1950s.
Latest News
FSHD Northeast & Cumbria Engagement Day
To celebrate World FSHD Day, Prof Giorgio Tasca & the JWMDRC are delighted to announce the 3rd annual FSHD Engagement Day in Newcastle on 15 August
Newcastle has a long history as a centre of international excellence in muscle disease diagnosis, care and research.
First established as the Muscular Dystrophy Laboratories at Newcastle General Hospital, the team here has grown over the years and now comprises a group of experts across many fields within muscular dystrophy who together form the John Walton Muscular Dystrophy Research Centre.
Whilst we are structured around four core areas of clinical care & diagnostics, basic research, clinical research and networks & collaborations it is the significant and important level of collaboration and linkage between these areas that is responsible for the success of the team as a whole.
One of the great strengths of the Centre is its multidisciplinary and cooperative approach, both within the team at Newcastle and with other leading experts around the world.
Genetic neuromuscular disease includes some very rare conditions and it is through establishing these partnerships that the biggest strides towards improving diagnosis, care and treatment for patients can be made.
The John Walton Muscular Dystrophy Research Centre team are members of the MRC Centre for Neuromuscular Diseases, a joint enterprise between University College London and Newcastle promoting translational research in neuromuscular diseases. The MRC Centre is a major source of support for activity in Newcastle, including the MRC Centre Biobank and for activities in magnetic resonance imaging (MRI). It also funds several PhD and clinical students in various disease areas.
In addition to this the team has, in the past five years, trained more than 20 visitors from five continents. Thanks to extensive international networking, in recent years the Centre has also become recognised for its leadership in the rare disease field more broadly and has become part of major global rare disease initiatives including the Global Alliance for Genomics and Health and the International Rare Diseases Research Consortium.
Professor Volker Straub leads the John Walton Muscular Dystrophy Research Centre and holds a joint appointment between Newcastle University and the NHS. With over 300 publications, Volker’s time is split between research and clinical commitments, all of which have a focus on neuromuscular disease whilst providing leadership across the five strands of the Centre.
Baseline characterisation of adults living with spinal muscular atrophy in the UK: insight from the Adult SMA REACH Real-World Data Collection Study
Neuromuscular Disorders 2026 Aug:65:106465. doi: 10.1016/j.nmd.2026.106465. Epub 2026 Jun 9.
Elena Karkkainen, Jess Page, Sonia Segovia, Laura Simms, Jose Verdu-Diaz, Aleks Carver, Jassi Michell-Sodhi, Stephanie Tanner, Dionne Moat, Robert Muni Lofra, Chiara Marini-Bettolo; Adult SMA REACH clinical network
Vamorolone for Duchenne Muscular Dystrophy: A Cross-Trial Efficacy Comparison With Classic Corticosteroids From the FOR-DMD Trial
Neurology. 2026 Jul 14;107(1):e214756. doi: 10.1212/WNL.0000000000214756. Epub 2026 May 27.
Paula R Clemens, Anders Berglund, Marianela Schiava, Meredith K James, Michael P McDermott, Katherine Bushby, Erik Lampa, Edward Thomas James Rochford, Leanne M Ward, Robert C Griggs, Eric P Hoffman, Michela Guglieri
Identification of prognostic biomarkers in a large cohort of patients with LGMD R2
Journal of Neurology. 2026 May 26;273(6):344. doi: 10.1007/s00415-026-13868-0.
Carla F Bolano-Diaz, Jose Verdu-Diaz, Dan Hao, Meredith K James, Laura Rufibach, Andrew Blamire, Harmen Reyngoudt, Pierre G Carlier, Heather Gordish-Dressman, Heather Hilsden, Simone Spuler, John Day, Kristi J Jones, Diana Bharucha-Goebel, Alan Pestronk, Maggie C Walter, Carmen Paradas, Tanya Stojkovic, Madoka Mori-Yoshimura, Elena Bravver, Elena Pegoraro, Jerry Mendell; Jain COS Consortium; Volker Straub, Jordi Diaz-Manera
Sensory neuronopathy secondary to gene therapy with AT845 for Pompe disease
Laura Pena-Guzman, Carla Bolano-Díaz, Cinta Lleixà, Luis Querol, Christina Trainor, Karen Suetterlin, Volker Straub, Jordi Díaz-Manera
Neurobehavioral Profiles in Young Steroid-Naive Boys With Duchenne Muscular Dystrophy: A Baseline Data Analysis From the FOR-DMD Trial
Neurology. 2026 Jun 9;106(11):e218094. doi: 10.1212/WNL.0000000000218094. Epub 2026 May 15.
Giulio Gadaleta, Chloe Geagan, Marianela Schiava, Pietro Riguzzi, Jos Hendriksen, Craig Campbell, Michael P McDermott, William B Martens, Stephanie J Gregory, Tiziana Enrica Mongini, Robert C Griggs, Michela Guglieri; FOR-DMD Investigators of the Muscle Study Group
Cracking the Code: Genotype-Phenotype Correlation Models in Sarcoglycanopathies
Annals of Clinical & Translational Neurology. 2026 Mar 19:10.1002/acn3.70361. doi: 10.1002/acn3.70361.
Leonela Luce, Goknur Selen Kocak, José Verdú-Díaz, Jorge Alonso-Pérez, Kristl G Claeys, Tanya Stojkovic, Gorka Fernández-Eulate, Pascal Laforêt, Najoua Miladi, Filipe Di Pace, Cristiane Araujo Martins Moreno, Edmar Zanoteli, Conrad C Weihl, Volker Straub, Ana Töpf, Jordi Díaz-Manera; Sarcoglycan European Cohort Consortium
John Walton
Lord Walton’s contribution to the field of muscle disease research and patient care is enormous. He was a leading figure in the field for over 50 years and trained many of the current leaders in the neuromuscular field.
Born locally in Rowlands Gill, John Walton qualified from Newcastle Medical School in 1945, then part of the University of Durham. In 1959 he co-founded the Muscular Dystrophy Campaign, now known as Muscular Dystrophy UK, of which he was Honorary Life President. He went on to become both a Consultant Neurologist and Professor of Neurology at Newcastle, and from 1971-1981 was Dean of Medicine at the University.
John Walton’s work in the 1950s was a milestone in the classification and description of muscular dystrophies as different entities. His landmark paper with Professor Nattrass in 1954 changed the research and diagnostic landscape for muscle disease.
It was John Walton’s pioneering work that saw his department at Newcastle first become recognised as a leader in neuromuscular disorders and established it as the internationally acclaimed centre for muscle disease research that it is today.
John Walton was awarded a Life Peerage, becoming Lord Walton of Detchant in 1989.
Sadly, Lord Walton passed away in April 2016.
Let's stay in touch Join our social media
Cookie consent
We use some essential cookies to make this website work.
We also use cookies set by other sites to help us deliver content from their services, like fonts and maps.