Pauline Hensman

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

Maurizio Scarpa, Zsuzsanna Almássy, Michael Beck et al. · Orphanet Journal of Rare Diseases · 2011 · 223 citations · Full text

Outcomes of Long-Term Treatment with Laronidase in Patients with Mucopolysaccharidosis Type I

Sarah Laraway, Jean Mercer, Elisabeth Jameson et al. · The Journal of Pediatrics · 2016 · 53 citations · Full text

Mucopolysaccharidosis Type, Long-term Treatment, Pathology +2

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

Alexander Broomfield, James Davison, Joseph Roberts et al. · Molecular Genetics and Metabolism · 2019 · 49 citations

Enzyme Replacement Therapy, Pediatrics, Pathology +2

Rapidly Progressive White Matter Involvement in Early Childhood: The Expanding Phenotype of Infantile Onset Pompe?

Alexander Broomfield, Joan Fletcher, Pauline Hensman et al. · JIMD Reports · 2017 · 30 citations · Full text

Assessment of musculoskeletal abnormalities in children with mucopolysaccharidoses using pGALS

Mercedes Chan, Ethan S Sen, Elizabeth Hardy et al. · Pediatric Rheumatology · 2014 · 21 citations · Full text