Compounds > glucose, (beta-d)-isomer
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glucose, (beta-d)-isomer and Glycogenosis

glucose, (beta-d)-isomer has been researched along with Glycogenosis in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19904 (66.67)18.7374
1990's0 (0.00)18.2507
2000's1 (16.67)29.6817
2010's1 (16.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Carrizo, ME; Curtino, JA; Issoglio, FM; Romero, JM1
Liebrand van Sambeek, R; Morava, E; van Diggelen, OP; van Essen, HZ; Wevers, R; Wortmann, SB1
Butterworth, J; Droadhead, DM1
Brouwer-Kelder, B; Donker-Koopman, WE; Hamers, MN; Loonen, C; Schram, AW; Tager, JM1
Broadhead, DM; Butterworth, J1
Blitzer, MG; Dunn, DW; Shapira, E; Temple, JK1

Other Studies

6 other study(ies) available for glucose, (beta-d)-isomer and Glycogenosis

ArticleYear
Structural and biochemical insight into glycogenin inactivation by the glycogenosis-causing T82M mutation.
    FEBS letters, 2012, Feb-03, Volume: 586, Issue:3

    Topics: Amino Acid Substitution; Animals; Apoenzymes; Crystallography, X-Ray; Enzyme Activation; Glucosides; Glucosyltransferases; Glycogen Storage Disease; Glycoproteins; Glycosylation; Hydrogen Bonding; Hydrolysis; Models, Molecular; Muscles; Mutant Proteins; Mutation; Protein Conformation; Rabbits; Uridine Diphosphate Glucose

2012
Biochemical characteristics and increased tetraglucoside excretion in patients with phosphorylase kinase deficiency.
    Journal of inherited metabolic disease, 2005, Volume: 28, Issue:5

    Topics: 1-Propanol; Biochemistry; Blood Chemical Analysis; Butanols; Cholesterol; Chromatography, Thin Layer; Erythrocytes; Family Health; Female; Glucosides; Glycogen Storage Disease; Hemoglobins; Heterozygote; Humans; Male; Oligosaccharides; Phosphorylase Kinase

2005
Diagnosis of Pompe's disease in cultured skin fibroblasts and primary amniotic fluid cells using 4-methylumbelliferyl-alpha-D-glucopyranoside as substrate.
    Clinica chimica acta; international journal of clinical chemistry, 1977, Jul-15, Volume: 78, Issue:2

    Topics: Amniotic Fluid; Cells, Cultured; Drug Stability; Female; Fibroblasts; Glucosidases; Glucosides; Glycogen Storage Disease; Glycogen Storage Disease Type II; Humans; Hydrogen-Ion Concentration; Hymecromone; Kinetics; Pregnancy; Prenatal Diagnosis; Skin

1977
Use of immobilized antibodies in investigating acid alpha-glucosidase in urine in relation to Pompe's disease.
    Biochimica et biophysica acta, 1979, Apr-12, Volume: 567, Issue:2

    Topics: alpha-Glucosidases; Glucosidases; Glucosides; Glycogen Storage Disease; Glycogen Storage Disease Type II; Hexosaminidases; Humans; Hydrogen-Ion Concentration; Immunoenzyme Techniques; Kinetics; Liver

1979
Pompe's disease: diagnosis in kidney and leucocytes using 4-methylumbelliferyl-alpha-D-glucopyranoside.
    Clinical genetics, 1978, Volume: 13, Issue:6

    Topics: alpha-Glucosidases; Glucosides; Glycogen Storage Disease; Glycogen Storage Disease Type II; Humans; Hymecromone; Kidney; Leukocytes; Umbelliferones

1978
The "muscular variant" of Pompe disease: clinical, biochemical and histologic characteristics.
    American journal of medical genetics, 1985, Volume: 21, Issue:3

    Topics: alpha-Glucosidases; Child, Preschool; Fibroblasts; Genes, Recessive; Genetic Variation; Glucosides; Glycogen Storage Disease; Glycogen Storage Disease Type II; Humans; Hymecromone; Leukocytes; Male; Muscles; Muscular Diseases; Respiratory Insufficiency

1985