maltotetraose has been researched along with Glycogen Storage Disease in 1 studies
*Glycogen Storage Disease: A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent liver involvement is presented. In others, more generalized storage of glycogen occurs, sometimes with prominent cardiac involvement. [MeSH]
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| de Vries, JM; Goudriaan, DA; Huijmans, JG; Reuser, AJ; Ruijter, GJ; Sluiter, W; van den Bosch, JC; van der Ploeg, AT; van Gelder, CM | 1 |
1 other study(ies) available for maltotetraose and Glycogen Storage Disease
| Article | Year |
|---|---|
Rapid ultraperformance liquid chromatography-tandem mass spectrometry assay for a characteristic glycogen-derived tetrasaccharide in Pompe disease and other glycogen storage diseases.
Topics: Adolescent; Adult; Age Factors; Aged; Child; Child, Preschool; Chromatography, Liquid; Glycogen; Glycogen Storage Disease; Glycogen Storage Disease Type II; Glycogen Storage Disease Type III; Glycogen Storage Disease Type IV; Humans; Infant; Infant, Newborn; Maltose; Middle Aged; Oligosaccharides; Reference Values; Spectrometry, Mass, Electrospray Ionization; Tandem Mass Spectrometry; Young Adult | 2012 |