Scientific Online Resource System

International Bulletin of Otorhinolaryngology

Mucopolysaccharidosis II (Hunter's syndrome)

Svetlan Simeonov

Abstract

.

Full Text


References

NEUFELD EF et al. In: The metabolic and molecular bases of inherited disease, 2001:3421–52.

WRAITH JE et al. Genet Med. 2008;10:508–16.

MARTIN R et al. Pediatrics. 2008; 121:e377–86.

BURTON BK et al. Eur J Pediatr. 2012; 171:631‒9.

SCARPA M. et al, Orphanet J Rare Dis. 2011; 72-89.

LINK B et al. Orthoped Rev. 2010; 2:56–64.

MENDELSOHN NJ et al. Genet Med. 2010; 12:816–22.

YOUNG ID, HARPER PS. Dev Med Child Neurol. 1983; 25:481‒9.

KEILMANN A. et al, Int J Pediatr Otorhinolaryngol. 2015 Feb; 79(2):115-8.

GAITINI L. et al, J Laryngol Otol. 1998 Apr; 112(4):380-2.

MEIKLE PJ et al. JAMA. 1999; 281(3):249–254.

CULLEN KA et al. National Health Statistics Reports 2009; 11:1–28.

MUENZER J. Rheumatology. 2011; 50: v4–v12.

TUSCHL K et al. Pediatr Neurol. 2005; 32(4):270–272.

SUMMARY OF PRODUCT CHARACTERISTICS: https://www.ema.europa.eu/documents/product-information/elaprase-epar-productinformation_en.pdf




DOI: http://dx.doi.org/10.14748/orl.v15i2.6710

Refbacks

Font Size


|