Page last updated: 2024-08-17

galactose and Deficiency, Hexosediphosphatase

galactose has been researched along with Deficiency, Hexosediphosphatase in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19904 (80.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hoffmann, B; Mayatepek, E; Meissner, T1
Förster, H1
Osang, M; Schaub, J1
Froesch, ER1
Cohn, RM; Segal, S; Yudkoff, M1

Reviews

1 review(s) available for galactose and Deficiency, Hexosediphosphatase

ArticleYear
Inborn errors of carbohydrate metabolism.
    Best practice & research. Clinical gastroenterology, 2010, Volume: 24, Issue:5

    Topics: Adult; Child; Dietary Carbohydrates; Fructose Intolerance; Fructose Metabolism, Inborn Errors; Fructose-1,6-Diphosphatase Deficiency; Galactose; Galactosemias; Glycogen Storage Disease; Humans; Infant; Liver Diseases; Liver Transplantation; Prognosis

2010

Other Studies

4 other study(ies) available for galactose and Deficiency, Hexosediphosphatase

ArticleYear
[Hypoglycemia. 3. Hypoglycemias caused by defined metabolic defects; hormonal regulation of blood glucose concentration and its disorders].
    Fortschritte der Medizin, 1976, Feb-12, Volume: 94, Issue:5

    Topics: Fructose-1,6-Diphosphatase Deficiency; Galactose; Gluconeogenesis; Glucosephosphate Dehydrogenase Deficiency; Glycogen; Glycogen Storage Disease; Glycoside Hydrolases; Humans; Hyperinsulinism; Hypoglycemia; Hypothyroidism; Insulin; Lactates; Leucine; Parathyroid Hormone; Phosphorylases; Pyruvate Carboxylase Deficiency Disease

1976
[Congenital enzyme deficiency in carbohydrate metabolism. Its significance for clinical pediatrics and human biochemical genetics (author's transl)].
    MMW, Munchener medizinische Wochenschrift, 1976, May-07, Volume: 118, Issue:19

    Topics: Carbohydrate Metabolism, Inborn Errors; Fructose Intolerance; Fructose-1,6-Diphosphatase Deficiency; Galactose; Galactosemias; Glycogen Storage Disease Type I; Glycogen Storage Disease Type II; Glycogen Storage Disease Type III; Glycogen Storage Disease Type VI; Glycogen Synthase; Humans; Infant; Infant, Newborn; Lactates; Liver; Phosphotransferases; Pyruvate Carboxylase Deficiency Disease; Pyruvate Dehydrogenase Complex Deficiency Disease; Racemases and Epimerases

1976
Disorders of fructose metabolism.
    Clinics in endocrinology and metabolism, 1976, Volume: 5, Issue:3

    Topics: Aging; Carbohydrate Metabolism, Inborn Errors; Fructose; Fructose Intolerance; Fructose-1,6-Diphosphatase Deficiency; Galactose; Humans; Infant; Infant, Newborn

1976
Errors of carbohydrate metabolism in infants and children: a survey.
    Clinical pediatrics, 1978, Volume: 17, Issue:11

    Topics: Carbohydrate Metabolism, Inborn Errors; Diarrhea; Fructokinases; Fructose Intolerance; Fructose-1,6-Diphosphatase Deficiency; Galactokinase; Galactose; Galactosemias; Glucose; Humans; Lactose Intolerance; Malabsorption Syndromes; Sucrase-Isomaltase Complex; Syndrome; Transferases; Uridine Diphosphate Galactose

1978