galactose has been researched along with Deficiency, Glucosephosphatase in 22 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 15 (68.18) | 18.7374 |
| 1990's | 4 (18.18) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 3 (13.64) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Boss, A; Derks, TGJ; Groen, AK; Heerschap, A; Hijmans, BS; Mithieux, G; Mutel, E; Oosterveer, MH; Rajas, F; Reijngoud, DJ; Soty, M; van Dijk, TH; Wolters, H | 1 |
| Antonopoulos, A; Dell, A; Föll, D; Haslam, SM; Letkemann, R; Marquardt, T; Podskabi, T; Wittkowski, H | 1 |
| GRASSI, A; TORCIGLIANI, A | 1 |
| HUIJING, F | 1 |
| Nuki, G; Parker, J | 1 |
| Bashan, N; Gopas, J; Horn, S; Peleg, N | 1 |
| Burchell, A; Hawkins, RA; Kamath, KR; Scott, HM | 1 |
| Applegarth, DA; Davidson, AG; Kirby, L; Rigg, JM; Tze, WJ; Wong, LT | 1 |
| Stamm, WE; Webb, DI | 1 |
| Osang, M; Schaub, J | 1 |
| Chalmers, RA; Ryman, BE; Watts, RW | 1 |
| Arashima, S; Matsuda, I; Mitsuyama, T; Nagai, B; Ohkubo, I; Oka, Y | 1 |
| Bartolozzi, G; Bernini, G; Marianelli, L; Nassi, P | 1 |
| Chibisov, IV; Popova, IA; Rosenfield, EL | 1 |
| Dykes, JR; Spencer-Peet, J | 1 |
| Bierich, JR; Rager, K; Schönberg, D | 1 |
| Mukhopadhyay, D; Rennert, OM | 1 |
| Fernandes, J; Huijing, F; van de Kamer, JH | 1 |
| Schöni, MH | 1 |
| Bashan, N; Moran, A; Moses, SW; Peleg, N; Potashnik, R | 2 |
22 other study(ies) available for galactose and Deficiency, Glucosephosphatase
| Article | Year |
|---|---|
Hepatocytes contribute to residual glucose production in a mouse model for glycogen storage disease type Ia.
Topics: alpha-Glucosidases; Animals; Disease Models, Animal; Galactose; Glucose; Glucose-6-Phosphatase; Glycerol; Glycogen Storage Disease Type I; Hepatocytes; Male; Mice | 2017 |
Partial correction of neutrophil dysfunction by oral galactose therapy in glycogen storage disease type Ib.
Topics: Administration, Oral; Antiporters; Female; Galactose; Genotype; Glucose; Glycogen Storage Disease Type I; Glycosylation; Humans; Hypoglycemia; Infant; Monosaccharide Transport Proteins; NADPH Oxidases; Neutrophils; Oxidative Stress; Young Adult | 2017 |
[Galactose, glucagon, BZ 55 and thyroid in hepatic glycogenosis (Gierke's disease)].
Topics: Carbutamide; Galactose; Glucagon; Glycogen Storage Disease; Glycogen Storage Disease Type I; Hormones; Humans; Thyroid Gland | 1960 |
GLYCOGEN STORAGE DISEASE. BIOCHEMICAL AND CLINICAL DATA IN SIXTEEN CASES.
Topics: Biochemical Phenomena; Biochemistry; Blood; Blood Glucose; Child; Galactose; Glucosidases; Glycogen Storage Disease; Glycogen Storage Disease Type I; Hepatomegaly; Humans; Infant; Infant, Newborn; Lactates; Leukocytes; Liver; Liver Diseases; Liver Glycogen; Phosphotransferases | 1965 |
Clinical and enzymological studies in a child with type I glycogen storage disease associated with partial deficiency of hepatic glucose-6-phosphatase.
Topics: Blood Glucose; Erythrocytes; Female; Follow-Up Studies; Galactose; Glucagon; Glucose-6-Phosphatase; Glucosidases; Glycogen Debranching Enzyme System; Glycogen Storage Disease Type I; Humans; Hypoxanthine Phosphoribosyltransferase; Infant; Kinetics; Liver; Liver Glycogen; Phosphoribosyl Pyrophosphate | 1980 |
Membrane glycoprotein modifications of G6PD deficient red blood cells.
Topics: Animals; beta-Galactosidase; Blotting, Western; Electrophoresis, Polyacrylamide Gel; Erythrocyte Membrane; Erythrocytes; Female; Galactose; Glycogen Storage Disease Type I; Hemostasis; Humans; Macrophages; Male; Mannose; Membrane Glycoproteins; Mice; Mice, Inbred BALB C; Phagocytosis | 1995 |
Multiple transport protein defects in a patient with glycogen storage disease type 1: GSD 1b/1c beta.
Topics: Antiporters; Blood Glucose; Galactose; Glucagon; Glycogen Storage Disease Type I; Humans; Infant; Kinetics; Male; Microsomes, Liver; Monosaccharide Transport Proteins; Phosphotransferases | 1995 |
Glycogen storage disease type I: effect of continuous nocturnal nasogastric feeding.
Topics: Child; Enteral Nutrition; Food, Formulated; Galactose; Glucagon; Glucose; Glucose Tolerance Test; Glycogen Storage Disease Type I; Humans; Infant; Male; Time Factors | 1978 |
Partial deficiency of hepatic glucose-6-phosphatase in an adult patient.
Topics: Adult; Arthritis, Rheumatoid; Biopsy, Needle; Drug Tolerance; Epinephrine; Female; Galactose; Glucose-6-Phosphatase; Glycogen Storage Disease Type I; Gout; Humans; Liver | 1975 |
[Congenital enzyme deficiency in carbohydrate metabolism. Its significance for clinical pediatrics and human biochemical genetics (author's transl)].
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 |
Studies on a patient with in vivo evidence of type I glycogenosis and normal enzyme activities in vitro.
Topics: Fructose-Bisphosphatase; Galactose; Glucagon; Glucose Tolerance Test; Glucose-6-Phosphatase; Glucosyltransferases; Glycogen Debranching Enzyme System; Glycogen Storage Disease Type I; Humans; Infant; Ketoglutaric Acids; Liver; Liver Glycogen; Male; Phosphorylases | 1978 |
Glucose-6-phosphatase activity in liver and blood platelets of two patients with glycogen storage disease type I.
Topics: Alanine; Blood Glucose; Blood Platelets; Child, Preschool; Female; Galactose; Glucagon; Glucose-6-Phosphatase; Glycerophosphates; Glycogen Storage Disease Type I; Humans; Liver; Liver Glycogen | 1978 |
[Type I glycogenosis. Description of 2 cases with hyperuricemia].
Topics: Biopsy; Child; Galactose; Glucagon; Glucose Tolerance Test; Glycogen Storage Disease Type I; Gout; Humans; Lactates; Lipids; Liver; Liver Glycogen; Male; Pyruvates; Uric Acid | 1975 |
Some cases of Type III glycogen storage disease.
Topics: Blood Glucose; Child; Child, Preschool; Erythrocytes; Female; Galactose; Glucose Tolerance Test; Glucosyltransferases; Glycogen; Glycogen Debranching Enzyme System; Glycogen Storage Disease; Glycogen Storage Disease Type I; Glycogen Storage Disease Type III; Humans; Hypoglycemia; Lactates; Liver; Male; Phosphorylases | 1976 |
Hepatic glycogen synthetase deficiency. Further studies on a family.
Topics: Adolescent; Blood Glucose; Child; Child, Preschool; Diagnosis, Differential; Fasting; Female; Galactose; Glucagon; Glucose; Glucose Tolerance Test; Glucosyltransferases; Glycogen; Glycogen Storage Disease Type I; Hexosaminidases; Humans; Hydrocortisone; Hypoglycemia; Infant; Insulin; Liver; Male; Metabolism, Inborn Errors | 1972 |
[Diagnosis of glycogenosis].
Topics: Diagnosis, Differential; Galactose; Glucagon; Glucose; Glucose Tolerance Test; Glucosidases; Glycogen Storage Disease; Glycogen Storage Disease Type I; Humans; Infant; Liver Diseases; Male | 1973 |
Endocrinological findings in patients with glycogenosis.
Topics: Blood Glucose; Fatty Acids, Nonesterified; Galactose; Glucagon; Glucosidases; Glycogen Storage Disease; Glycogen Storage Disease Type I; Growth Hormone; Humans; Hydrocortisone; Insulin | 1973 |
Diazoxide in von Gierke's disease.
Topics: Animals; Blood Glucose; Carbohydrate Metabolism, Inborn Errors; Child; Diazoxide; Dogs; Galactose; Glucose; Glucose Tolerance Test; Glycogen Storage Disease; Glycogen Storage Disease Type I; Hirsutism; Humans; Infant; Liver Glycogen; Male; Rats | 1968 |
A screening method for liver glycogen diseases.
Topics: Adolescent; Biological Assay; Child; Child, Preschool; Clinical Enzyme Tests; Female; Fructose; Galactose; Glucagon; Glucose Tolerance Test; Glucosyltransferases; Glycogen Storage Disease; Glycogen Storage Disease Type I; Humans; Infant; Liver Diseases; Liver Function Tests; Male; Mass Screening | 1969 |
[Too small, too large, too fat, too thin?].
Topics: Glycogen Storage Disease Type I; Hexoses; Humans; Neutrophils | 2013 |
Uptake and transport of hexoses into polymorphonuclear leukocytes of patients with glycogen storage disease type 1b.
Topics: 3-O-Methylglucose; Adolescent; Adult; Biological Transport; Child; Child, Preschool; Deoxyglucose; Glycogen Storage Disease Type I; Hexoses; Humans; Infant; Methylglucosides; Neutrophils; Pentose Phosphate Pathway; Phosphorylation | 1990 |
Hexose uptake and transport in polymorphonuclear leukocytes from patients with glycogen storage disease Ib.
Topics: 3-O-Methylglucose; Adolescent; Biological Transport, Active; Child, Preschool; Deoxyglucose; Glycogen Storage Disease Type I; Hexoses; Humans; In Vitro Techniques; Infant; Kinetics; Methylglucosides; Neutrophils; Pentose Phosphate Pathway; Phosphorylation | 1990 |