Effect of 6 years of enzyme replacement therapy on plasma and urine glycosaminoglycans in attenuated MPS I patients
Author:
Publisher
Oxford University Press (OUP)
Subject
Biochemistry
Link
http://academic.oup.com/glycob/article-pdf/20/10/1259/5846985/cwq088.pdf
Reference33 articles.
1. Stability of urinary glycosaminoglycans in patients with mucopolysaccharidoses
2. Direct quantitation of glycosaminoglycans in 2 mL of urine from patients with mucopolysaccharidoses.
3. Structural Analysis of Bikunin Glycosaminoglycan
4. Reliability of 1,9-dimethylmethylene blue tests in comparison to agarose gel electrophoresis for quantification of urinary glycosaminoglycans
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1. Application of pathogenicity scores as diagnostic and prognostic markers for MPS disorders: In-silico analysis in MPS I;2023-01-09
2. Glycosaminoglycan signatures in body fluids of mucopolysaccharidosis type II mouse model under long-term enzyme replacement therapy;Journal of Molecular Medicine;2022-07-11
3. The Value of Case Reports in Systematic Reviews from Rare Diseases. The Example of Enzyme Replacement Therapy (ERT) in Patients with Mucopolysaccharidosis Type II (MPS-II);International Journal of Environmental Research and Public Health;2020-09-10
4. Enzyme replacement therapy for mucopolysaccharidoses; past, present, and future;Journal of Human Genetics;2019-08-27
5. Total and single species of uronic acid-bearing glycosaminoglycans in urine of newborns of 2–3 days of age for early diagnosis application;Clinica Chimica Acta;2016-12
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