Menu

Newcastle to coordinate Neuromuscular European Reference Network

We are delighted to announce that the Neuromuscular European Reference Network (EURO-NMD) has passed the final step of the evaluation process and was approved by the Board of Member States. European Reference Networks (ERN) create …


Article published on 20 December 2016

Outcome of the British EU referendum

The outcome of the British EU referendum makes this a sad day for the John Walton Muscular Dystrophy Research Centre, for research and education in the UK and for British patients with rare diseases. A …


Article published on 27 July 2016

Drug development project receives £4.6m to help boys with rare illness

Millions of pounds have been invested in a drug development programme to help boys with a rare life-limiting disease The John Walton Muscular Dystrophy Research Centre at Newcastle University has received £4.6 million from the …


Article published on 16 March 2016

Princess Eugenie visits centre

Princess Eugenie of York returned to the University, where she herself studied, to find out about the pioneering research undertaken at the John Walton Muscular Dystrophy Research Centre. Her Royal Highness met with Newcastle University’s …


Article published on 16 October 2015
Menu