glucose tetrasaccharide has been researched along with Amylo-1,6-Glucosidase Deficiency in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (50.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Austin, S; Bali, D; Clinton, LK; Halaby, CA; Kishnani, PS; Mavis, AM; Pendyal, S; Schooler, GR; Smith, B; Stefanescu, E; Upadia, J; Young, SP | 1 |
| Chester, MA; Häger, A; Loonen, C; Lundblad, A; Sjöblad, S; Tager, JM; Zopf, D | 1 |
2 other study(ies) available for glucose tetrasaccharide and Amylo-1,6-Glucosidase Deficiency
| Article | Year |
|---|---|
Liver fibrosis during clinical ascertainment of glycogen storage disease type III: a need for improved and systematic monitoring.
Topics: Adolescent; Biomarkers; Child; Child, Preschool; Cholesterol; Female; Glycogen; Glycogen Storage Disease; Glycogen Storage Disease Type I; Glycogen Storage Disease Type III; Humans; Liver; Liver Cirrhosis; Liver Diseases; Male; Oligosaccharides; Transaminases; Triglycerides; Young Adult | 2019 |
Increased urinary excretion of a glycogen-derived tetrasaccharide in heterozygotes with glycogen storage diseases type II and III.
Topics: Adult; Aged; Child; Child, Preschool; Female; Glycogen Storage Disease; Glycogen Storage Disease Type II; Glycogen Storage Disease Type III; Heterozygote; Humans; Male; Middle Aged; Oligosaccharides | 1983 |