Liquid Chromatographic Assay for a Glucose Tetrasaccharide, a Putative Biomarker for the Diagnosis of Pompe Disease
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference26 articles.
1. The Metabolic and Molecular Bases of Inherited Disease;Hirschhorn,1995
2. Clinical and metabolic correction of pompe disease by enzyme therapy in acid maltase-deficient quail.
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4. Systemic correction of the muscle disorder glycogen storage disease type II after hepatic targeting of a modified adenovirus vector encoding human acid- -glucosidase
5. Increased Excretion of a Glucose-Containing Tetrasaccharide in the Urine of a Patient with Glycogen Storage Disease Type II (Pompe's Disease)
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2. Development of a rapid simultaneous assay of two urinary tetrasaccharide metabolites using differential ion mobility and tandem mass spectrometry and its application to patients with glycogen storage disease (type Ib and II);Analytical and Bioanalytical Chemistry;2023-09-29
3. Rapid ultra-performance liquid chromatography-tandem mass spectrometry method for the simultaneous determination of three characteristic urinary saccharide metabolites in patients with glycogen storage diseases (type Ⅰb and Ⅱ);Journal of Chromatography B;2023-09
4. Combined targeted and untargeted high-resolution mass spectrometry analyses to investigate metabolic alterations in pompe disease;Metabolomics;2023-03-29
5. Development of a kit for urine collection on filter paper as an alternative for Pompe disease screening and monitoring by LC-HRMS;Analytical Methods;2023
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