Dr Simon Jones was born in Northern Ireland and attended Edinburgh University Medical School, qualifying with a BSc in neurosciences. He moved to London and trained in paediatrics at Guy’s and St Thomas’ Hospital. Simon has been working at the Willink Biochemical Genetics Unit, now part of Genetic Medicine at St Mary’s Hospital, Manchester, since September 2005. He has been principal investigator or actively involved in many phase I-IV international multicentre trials of enzyme replacement therapy for lysosomal storage disorders. Since 2008 he has been a Consultant in paediatric inherited metabolic diseases at the Willink Unit.
General metabolic, glycogen storage disease, lysosomal storage disease