Biomarkers for lysosomal storage disorders: identification and application as exemplified by chitotriosidase in Gaucher disease-Reference-Cited by-同舟云学术

Biomarkers for lysosomal storage disorders: identification and application as exemplified by chitotriosidase in Gaucher disease

Published:2008-04 Issue:s457 Volume:97 Page:7-14
ISSN:0803-5253
Container-title:Acta Paediatrica
language:en
Short-container-title:Acta Paediatrica

Author:

Aerts Johannes M,van Breemen Marielle J,Bussink Anton P,Ghauharali Karen,Sprenger Richard,Boot Rolf G,Groener Johanna E,Hollak Carla E,Maas Mario,Smit Suzanne,Hoefsloot Huub C,Smilde Age K,Vissers Johannes PC,de Jong Sheryas,Speijer Dave,de Koster Chris G

Publisher

Wiley

Subject

General Medicine,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.2007.00641.x/fullpdf

Reference64 articles.

1. 1. EMEA . Report on the EMEA/CHMP Biomarkers Workshop, European Medicines Agency . 2006 : http://www.emea.europa.eu/pdfs/human/biomarkers/42720905en.pdf.

2. Quantification of Skeletal Involvement in Adults with Type I Gaucher's Disease: Fat Fraction Measured by Dixon Quantitative Chemical Shift Imaging as a Valid Parameter

3. Lysosomal storage diseases

4. Demonstration of a deficiency of glucocerebroside-cleaving enzyme in Gaucher's disease.

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