Page last updated: 2024-09-05

glucose tetrasaccharide and glycogen

glucose tetrasaccharide has been researched along with glycogen in 7 studies

Compound Research Comparison

Studies (glucose tetrasaccharide)	Trials (glucose tetrasaccharide)	Recent Studies (post-2010) (glucose tetrasaccharide)	Studies (glycogen)	Trials (glycogen)	Recent Studies (post-2010) (glycogen)
21	2	9	25,566	576	3,794

Research

Studies (7)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (28.57)	29.6817
2010's	5 (71.43)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Amalfitano, A; An, Y; Chen, YT; Corz, D; Kishnani, PS; Millington, DS; Young, SP	1
Bali, D; Corzo, D; Kishnani, PS; Millington, DS; Thurberg, BL; Young, SP; Zhang, H	1
Bali, DS; Bashir, MR; Goldstein, JL; Kishnani, PS; Laforet, P; Millington, DS; Piraud, M; Rehder, C; Young, SP; Zhang, H	1
Higuchi, I; Kawano, Y; Maegaki, Y; Maruyama, S; Nanba, E; Narita, A; Ohno, K; Toyoshima, M; Yonee, C; Young, SP	1
Bobillo Lobato, J; Durán Parejo, P; Jiménez Jiménez, LM; Tejero Díez, P	1
Ahmadipour, F; Aryani, O; Fani, S; Houshmand, M; Kamalidehghan, B; Khalili, E; Manshadi, MD; Tondar, M	1
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

Trials

2 trial(s) available for glucose tetrasaccharide and glycogen

Article	Year
Long-term monitoring of patients with infantile-onset Pompe disease on enzyme replacement therapy using a urinary glucose tetrasaccharide biomarker. Genetics in medicine : official journal of the American College of Medical Genetics, 2009, Volume: 11, Issue:7 Topics: Alanine Transaminase; alpha-Glucosidases; Aspartate Aminotransferases; Biomarkers; Creatine Kinase; Glycogen; Glycogen Storage Disease Type II; Humans; Infant; Infant, Newborn; Monitoring, Physiologic; Muscle, Skeletal; Oligosaccharides; Tandem Mass Spectrometry	2009
[Tetra-saccharide glucose as a diagnostic biomarker for Pompe disease: a study with 35 patients]. Medicina clinica, 2013, Aug-04, Volume: 141, Issue:3 Topics: Adolescent; Adult; Age of Onset; Area Under Curve; Biomarkers; Child; Child, Preschool; Chromatography, High Pressure Liquid; Female; Glycogen; Glycogen Storage Disease Type II; Humans; Infant; Male; Middle Aged; Oligosaccharides; ROC Curve; Young Adult	2013

Article

Year

Long-term monitoring of patients with infantile-onset Pompe disease on enzyme replacement therapy using a urinary glucose tetrasaccharide biomarker.

Genetics in medicine : official journal of the American College of Medical Genetics, 2009, Volume: 11, Issue:7

Topics: Alanine Transaminase; alpha-Glucosidases; Aspartate Aminotransferases; Biomarkers; Creatine Kinase; Glycogen; Glycogen Storage Disease Type II; Humans; Infant; Infant, Newborn; Monitoring, Physiologic; Muscle, Skeletal; Oligosaccharides; Tandem Mass Spectrometry

2009

[Tetra-saccharide glucose as a diagnostic biomarker for Pompe disease: a study with 35 patients].

Medicina clinica, 2013, Aug-04, Volume: 141, Issue:3

Topics: Adolescent; Adult; Age of Onset; Area Under Curve; Biomarkers; Child; Child, Preschool; Chromatography, High Pressure Liquid; Female; Glycogen; Glycogen Storage Disease Type II; Humans; Infant; Male; Middle Aged; Oligosaccharides; ROC Curve; Young Adult

2013

Other Studies

5 other study(ies) available for glucose tetrasaccharide and glycogen

Article	Year
Glucose tetrasaccharide as a biomarker for monitoring the therapeutic response to enzyme replacement therapy for Pompe disease. Molecular genetics and metabolism, 2005, Volume: 85, Issue:4 Topics: alpha-Amylases; alpha-Glucosidases; Biomarkers; Case-Control Studies; Glucan 1,4-alpha-Glucosidase; Glycogen; Glycogen Storage Disease Type II; Humans; Monitoring, Physiologic; Oligosaccharides	2005
Assessing disease severity in Pompe disease: the roles of a urinary glucose tetrasaccharide biomarker and imaging techniques. American journal of medical genetics. Part C, Seminars in medical genetics, 2012, Feb-15, Volume: 160C, Issue:1 Topics: Adult; Age Factors; Aged; alpha-Glucosidases; Biomarkers; Child; Child, Preschool; Diagnostic Imaging; Disease Progression; Enzyme Replacement Therapy; Glycogen; Glycogen Storage Disease Type II; Humans; Infant; Infant, Newborn; Middle Aged; Muscle, Skeletal; Mutation; Oligosaccharides; Prognosis; Sequence Analysis, DNA; Treatment Outcome; Young Adult	2012
Quantitative computed tomography for enzyme replacement therapy in Pompe disease. Brain & development, 2012, Volume: 34, Issue:10 Topics: alpha-Glucosidases; Child, Preschool; Enzyme Replacement Therapy; Female; Glycogen; Glycogen Storage Disease Type II; Humans; Liver; Muscle, Skeletal; Oligosaccharides; Tomography, X-Ray Computed	2012
A newly identified c.1824_1828dupATACG mutation in exon 13 of the GAA gene in infantile-onset glycogen storage disease type II (Pompe disease). Molecular biology reports, 2014, Volume: 41, Issue:9 Topics: alpha-Glucosidases; Cardiomyopathies; Consanguinity; Exons; Genetic Predisposition to Disease; Genome-Wide Association Study; Genome, Human; Genotype; Genotyping Techniques; Glucan 1,4-alpha-Glucosidase; Glycogen; Glycogen Storage Disease Type II; Humans; Infant; Iran; Male; Mutation; Oligosaccharides; Sequence Analysis, DNA	2014
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