S. Wendt

A phase II/III clinical study of enzyme replacement therapy with idursulfase in mucopolysaccharidosis II (Hunter syndrome)

C. Eng, M. Shinawi, U. Ramaswami, 2006, Genetics in Medicine.

Enzyme replacement therapy with agalsidase alfa in children with Fabry disease

U. Ramaswami, G. Pintos-Morell, R. Parini, 2007, Acta paediatrica.

Successful pregnancy outcome in a patient with Fabry disease receiving enzyme replacement therapy with agalsidase alfa

C. Whybra, C. Kampmann, M. Beck, 2005, Journal of Inherited Metabolic Disease.