CCL18: A urinary marker of Gaucher cell burden in Gaucher patients
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/s10545-006-0318-8
Reference20 articles.
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2. Aerts JM, Hollak C, Boot R, et al (2003) Biochemistry of glycosphingolipids storage disorders: implications for therapeutic intervention. Philos Trans R Soc Lond B Biol Sci 358: 905–914.
3. Aguilera B, Ghauharali-Van Der Vlugt K, Helmond MT, et al (2003) Transglycosidase activity of chitotriosidase: improved enzymatic assay for the human macrophage chitinase. J Biol Chem 278: 40911–40916.
4. Baldellou A, Andria G, Campbell PE, et al (2004) Paediatric non-neuronopathic Gaucher disease: recommendations for treatment and monitoring. Eur J Pediatr 163: 67–75.
5. Barton NW, Brady RO, Dambrosia JM, et al (1991) Replacement therapy for inherited enzyme deficiency: macrophage-targeted glucocerebrosidase for Gaucher's disease. N Engl J Med 324: 1464–1470.
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