Compounds > glucose tetrasaccharide
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glucose tetrasaccharide and Glycogenosis

glucose tetrasaccharide has been researched along with Glycogenosis in 6 studies

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 Glycogenosis

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