Plasmatic and Urinary Glycosaminoglycans Characterization in Mucopolysaccharidosis II Patient Treated with Enzyme-Replacement Therapy with Idursulfase-Reference-Cited by-同舟云学术

Plasmatic and Urinary Glycosaminoglycans Characterization in Mucopolysaccharidosis II Patient Treated with Enzyme-Replacement Therapy with Idursulfase

Published:2011 Issue: Volume: Page:79-90
ISSN:2192-8304
Container-title:JIMD Reports
language:
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Author:

Coppa Giovanni V.,Buzzega Dania,Zampini Lucia,Maccari Francesca,Santoro Lucia,Galeotti Fabio,Galeazzi Tiziana,Gabrielli Orazio,Volpi Nicola

Publisher

Springer Berlin Heidelberg

Link

http://link.springer.com/content/pdf/10.1007/8904_2011_75

Reference33 articles.

1. Alcalde-Martín C, Muro-Tudelilla JM, Cancho-Candela R et al (2010) First experience of enzyme replacement therapy with idursulfase in Spanish patients with Hunter syndrome under 5 years of age: case observations from the Hunter Outcome Survey (HOS). Eur J Med Genet 53:371–377

2. Burlingame RW, Thomas GH, Stevens RL et al (1981) Direct quantitation of glycosaminoglycans in 2 mL of urine from patients with mucopolysaccharidoses. Clin Chem 27:124–128

3. Buzzega D, Pederzoli F, Maccari F et al (2010) Comparison of CPC and CETAB extractive procedures for quantification and characterization of human urinary glycosaminoglycans. Clin Chem Lab Med 48:1133–1139

4. Chi L, Wolff JJ, Laremore TN et al (2008) Structural analysis of bikunin glycosaminoglycan. J Am Chem Soc 130:2617–2625

5. Coppa GV, Singh J, Nichols BL et al (1973) Urinary excretion of disulfated disaccharides in hunter syndrome: correction by infusion of a serum fraction. Anal Lett 6:225–229

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