C. Stewart

发表

Response of 33 UK patients with infantile-onset Pompe disease to enzyme replacement therapy

A. Broomfield, S. Santra, A. Chakrapani, 2016, Journal of Inherited Metabolic Disease.

Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease

L. de Meirleir, J. Zeman, P. Hensman, 2011, Orphanet journal of rare diseases.

Ten years of enzyme replacement therapy in paediatric onset mucopolysaccharidosis II in England.

U. Ramaswami, A. Broomfield, P. Hensman, 2020, Molecular genetics and metabolism.

Management of the behavioural manifestations of Hunter syndrome.

Jane Roberts, S. Kearney, C. Stewart, 2016, British journal of nursing.