Author:
Langereis Eveline J.,Wagemans Tom,Kulik Wim,Lefeber Dirk J.,van Lenthe Henk,Oussoren Esmee,van der Ploeg Ans T.,Ruijter George J.,Wevers Ron A.,Wijburg Frits A.,van Vlies Naomi
Publisher
Public Library of Science (PLoS)
Reference27 articles.
1. The Metabolic and Molecular Bases of Inherited Disease;EF Neufeld,2014
2. Braulke T, Raas-Rothschild A, Kornfeld S. I-cell disease and pseudo-Hurler polydystrophy: Disorders of lysosomal enzyme phosphorilation and localization. In: Valle D, Beaudet A, Vogelstein B, Kinzler K, Antonarakis S, Ballabio A, et al., editors. The Metabolic & Molecular Basis of Inherited Disease. 2014. pp. 3469–82.
3. Measuring urinary glycosaminoglycans in the presence of protein: An improved screening procedure for mucopolysaccharidoses based on dimethylmethylene blue;JGN De Jong;Clin Chem,1992
4. Dimethylmethylene blue-based spectrophotometry of glycosaminoglycans in untreated urine: a rapid screening procedure for mucopolysaccharidoses;JG De Jong;Clin Chem,1989
5. Development and Testing of New Screening Method for Keratan Sulfate in Mucopolysaccharidosis IVA;S Tomatsu;Pediatr Res,2004
Cited by
37 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献