Hunter syndrome (MPS II) publications

Burton BK and Giugliani R. Diagnosing Hunter syndrome in pediatric practice: practical considerations and common pitfalls. Eur J Pediatr 2012; 171(4): 631–9. www.ncbi.nlm.nih.gov/pubmed/22383073

Giugliani R, et al. Guidelines for diagnosis and treatment of Hunter Syndrome for clinicians in Latin America. Genet Mol Biol 2014; 37(2): 315–29. www.ncbi.nlm.nih.gov/pubmed/25071396

Holt JB, et al. Natural progression of neurological disease in mucopolysaccharidosis type II. Pediatrics 2011; 127(5) :e1258–65. www.ncbi.nlm.nih.gov/pubmed/21518713

Kamin W. Diagnosis and management of respiratory involvement in Hunter syndrome. Acta Paediatr Suppl 2008; 97(457): 57–60. www.ncbi.nlm.nih.gov/pubmed/18339190

Kampmann C, et al. Prevalence and characterization of cardiac involvement in Hunter syndrome. J Pediatr 2011; 159(2): 327–31.e2. www.ncbi.nlm.nih.gov/pubmed/21529823

Keilmann A, et al. Hearing loss in patients with mucopolysaccharidosis II: data from HOS – the Hunter Outcome Survey. J Inherit Metab Dis. 2012; 35(2): 343–53. www.ncbi.nlm.nih.gov/pubmed/21866356

Link B, et al. Orthopedic manifestations in patients with mucopolysaccharidosis type II (Hunter syndrome) enrolled in the Hunter Outcome Survey. Orthop Rev (Pavia) 2010; 2(2): e16. www.ncbi.nlm.nih.gov/pubmed/21808707

Martin R, et al. Recognition and diagnosis of mucopolysaccharidosis II (Hunter syndrome). Pediatrics 2008; 121(2): e377–86. www.ncbi.nlm.nih.gov/pubmed/18245410

Mendelsohn NJ, et al. Importance of surgical history in diagnosing mucopolysaccharidosis type II (Hunter syndrome): data from the Hunter Outcome Survey. Genet Med 2010; 12(12): 816–22. www.ncbi.nlm.nih.gov/pubmed/21045710

Muenzer J, et al. Multidisciplinary management of Hunter syndrome. Pediatrics 2009; 124(6): e1228–39. www.ncbi.nlm.nih.gov/pubmed/19901005

Muenzer J. Overview of the mucopolysaccharidoses. Rheumatology (Oxford) 2011; 50 Suppl 5: v4–12. www.ncbi.nlm.nih.gov/pubmed/22210669

Scarpa M, et al. Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease. Orphanet J Rare Dis 2011; 6: 72. www.ncbi.nlm.nih.gov/pubmed/22059643

Wraith JE, et al. Initial report from the Hunter Outcome Survey. Genet Med 2008; 10(7): 508–16. www.ncbi.nlm.nih.gov/pubmed/18580692