Compounds > glucose tetrasaccharide
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glucose tetrasaccharide and Glycogen Storage Disease

glucose tetrasaccharide has been researched along with Glycogen Storage Disease in 6 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]

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19901 (16.67)18.7374
1990's1 (16.67)18.2507
2000's0 (0.00)29.6817
2010's2 (33.33)24.3611
2020's2 (33.33)2.80

Authors

AuthorsStudies
de Boer, F; Derks, TGJ; Fokkert-Wilts, MJ; Heiner-Fokkema, MR; Hoogeveen, IJ; Maatman, RGHJ; van der Krogt, J1
Austin, SL; Khan, AA; Kishnani, PS; Young, SP1
Austin, S; Bali, D; Clinton, LK; Halaby, CA; Kishnani, PS; Mavis, AM; Pendyal, S; Schooler, GR; Smith, B; Stefanescu, E; Upadia, J; Young, SP1
Bainbridge, K; Burke, D; Finnegan, N; Franses, R; Heales, S; Lam, A; Manwaring, V; Prunty, H; Vellodi, A1
Chester, MA; Häger, A; Loonen, C; Lundblad, A; Sjöblad, S; Tager, JM; Zopf, D1
Oberholzer, K; Sewell, AC1

Other Studies

6 other study(ies) available for glucose tetrasaccharide and Glycogen Storage Disease

ArticleYear
The multiple faces of urinary glucose tetrasaccharide as biomarker for patients with hepatic glycogen storage diseases.
    Genetics in medicine : official journal of the American College of Medical Genetics, 2020, Volume: 22, Issue:11

    Topics: Biomarkers; Glycogen Storage Disease; Glycogen Storage Disease Type II; Humans; Liver; Oligosaccharides

2020
Response to Heiner-Fokkema et al.
    Genetics in medicine : official journal of the American College of Medical Genetics, 2020, Volume: 22, Issue:11

    Topics: Biomarkers; Glycogen Storage Disease; Humans; Oligosaccharides; Urinary Tract

2020
Liver fibrosis during clinical ascertainment of glycogen storage disease type III: a need for improved and systematic monitoring.
    Genetics in medicine : official journal of the American College of Medical Genetics, 2019, Volume: 21, Issue:12

    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
Urine analysis of glucose tetrasaccharide by HPLC; a useful marker for the investigation of patients with Pompe and other glycogen storage diseases.
    Journal of inherited metabolic disease, 2012, Volume: 35, Issue:2

    Topics: Biomarkers; Child; Child, Preschool; Chromatography, High Pressure Liquid; Enzyme Replacement Therapy; Female; Glycogen Storage Disease; Glycogen Storage Disease Type II; Humans; Infant; Male; Middle Aged; Oligosaccharides

2012
Increased urinary excretion of a glycogen-derived tetrasaccharide in heterozygotes with glycogen storage diseases type II and III.
    Lancet (London, England), 1983, Apr-30, Volume: 1, Issue:8331

    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
Unique oligosaccharide (apparently glucotetrasaccharide) in urine of patients with glycogen storage diseases.
    Clinical chemistry, 1990, Volume: 36, Issue:7

    Topics: Glycogen Storage Disease; Humans; Oligosaccharides

1990