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Acta Neurologica Taiwanica|October 29, 2004
The clinical presentation of lysosomal storage disordersJames E WraithTherapeutics and Clinical Risk Management|December 4, 2009
New therapies in the management of Niemann-Pick type C disease: clinical utility of miglustatJames E Wraith, Jackie ImrieThe Cochrane Database of Systematic Reviews|October 3, 2013
Enzyme replacement therapy with laronidase (Aldurazyme) for treating mucopolysaccharidosis type IElisabeth Jameson, Simon Jones, James E WraithPediatrics|August 3, 2007
Management guidelines for mucopolysaccharidosis VIRoberto Giugliani, Paul Harmatz, James E WraithThe Cochrane Database of Systematic Reviews|November 22, 2013
Enzyme replacement therapy with laronidase (Aldurazyme(®)) for treating mucopolysaccharidosis type IElisabeth Jameson, Simon Jones, James E WraithPediatrics|January 2, 2009
Mucopolysaccharidosis I: management and treatment guidelinesJoseph Muenzer, James E Wraith, Lorne A Clarke, et al.Molecular Genetics and Metabolism|June 1, 2013
Does early use of enzyme replacement therapy alter the natural history of mucopolysaccharidosis I? Experience in three siblingsSarah Laraway, Catherine Breen, Jean Mercer, et al.The Annals of Otology, Rhinology, and Laryngology|September 13, 2014
Airway-related symptoms and surgeries in patients with mucopolysaccharidosis IPamela Arn, Iain A Bruce, James E Wraith, et al.The Lancet. Neurology|August 11, 2007
Miglustat for treatment of Niemann-Pick C disease: a randomised controlled studyMarc C Patterson, Darleen Vecchio, Helena Prady, et al.Pediatric Rehabilitation|June 19, 2004
Physical performance testing in mucopolysaccharidosis I: a pilot studyHelene M Dumas, Maria A Fragala, Stephen M Haley, et al.Pageof 4