acebutolol has been researched along with Glycogenosis in 19 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 18 (94.74) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (5.26) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| de Vries, JM; Goudriaan, DA; Huijmans, JG; Reuser, AJ; Ruijter, GJ; Sluiter, W; van den Bosch, JC; van der Ploeg, AT; van Gelder, CM | 1 |
| Carey, WF; Nelson, PV; Pollard, AC | 1 |
| Beratis, NG; Hirschhorn, K; LaBadie, GU | 1 |
| Seiter, CW; Summer, GK | 1 |
| Rosenfeld, EL | 1 |
| Cox, RP; Dancis, J; Hutzler, J; Lynfield, J | 1 |
| Alexandre, Y; Dreyfus, JC | 1 |
| de Barsy, T; Devos, P; Hers, HG; Jacquemin, P | 1 |
| Fluharty, AL; Kihara, H; Porter, MT; Scott, ML; Towner, JW; Wilson, MG | 1 |
| Hers, HG | 1 |
| Brown, BI; Brown, DH | 1 |
| Angelini, C; Engel, AG | 1 |
| Angelini, C; Engel, AG; Titus, JL | 1 |
| Hülsmann, WC; Koster, JF; Slee, RG | 1 |
| Fernandes, J | 1 |
| de Barsy, T; Hers, HG; Jacquemin, P; Van Hoof, F | 1 |
| Rosenkranz, A | 1 |
| Brown, BI; Brown, DH; Jeffrey, PL | 1 |
| Palmer, TN | 1 |
2 review(s) available for acebutolol and Glycogenosis
| Article | Year |
|---|---|
Alpha-glucosidases (gamma-amylases) in human and animal organisms.
Topics: Amylases; Amyloidosis; Animals; Chromatography, Gel; Chromatography, Ion Exchange; Enzyme Activation; Glucosidases; Glycogen; Glycogen Storage Disease; Humans; Liver; Maltose; Muscles; Rabbits; Rats | 1975 |
Enzyme replacement in Pompe disease: an attempt with purified human acid alpha-glucosidase.
Topics: Cardiomyopathies; Fibroblasts; Glucose; Glucosidases; Glycogen; Glycogen Storage Disease; Humans; Infant; Infusions, Parenteral; Leukocytes; Liver; Male; Maltose; Microscopy, Electron; Muscles; Placenta; Skin; Syndrome | 1973 |
17 other study(ies) available for acebutolol and Glycogenosis
| Article | Year |
|---|---|
Rapid ultraperformance liquid chromatography-tandem mass spectrometry assay for a characteristic glycogen-derived tetrasaccharide in Pompe disease and other glycogen storage diseases.
Topics: Adolescent; Adult; Age Factors; Aged; Child; Child, Preschool; Chromatography, Liquid; Glycogen; Glycogen Storage Disease; Glycogen Storage Disease Type II; Glycogen Storage Disease Type III; Glycogen Storage Disease Type IV; Humans; Infant; Infant, Newborn; Maltose; Middle Aged; Oligosaccharides; Reference Values; Spectrometry, Mass, Electrospray Ionization; Tandem Mass Spectrometry; Young Adult | 2012 |
A micro-radiochemical assay for alpha-1,4-glucosidase and its use in the assessment of type II glycogenosis (Pompe's disease).
Topics: Amnion; Cell Line; Clinical Enzyme Tests; Fibroblasts; Glucosidases; Glycogen Storage Disease; Glycogen Storage Disease Type II; Humans; Hydrogen-Ion Concentration; Leukocytes; Maltose; Time Factors | 1977 |
Characterization of the molecular defect in infantile and adult acid alpha-glucosidase deficiency fibroblasts.
Topics: Adult; alpha-Glucosidases; Antibody Formation; Cross Reactions; Electrophoresis, Polyacrylamide Gel; Electrophoresis, Starch Gel; Female; Fibroblasts; Genes; Glucosidases; Glycogen Storage Disease; Glycogen Storage Disease Type II; Humans; Hydrogen-Ion Concentration; Immunodiffusion; Infant; Male; Maltose; Mutation; Placenta; Pregnancy; Skin | 1978 |
Glycogen metabolism in human skin fibroblasts. Influence of maltose on the activity of acid alpha-1, 4-glucosidase.
Topics: Adolescent; Cells, Cultured; Culture Media; Female; Fetus; Fibroblasts; Glucose; Glucosidases; Glycogen; Glycogen Storage Disease; Humans; Infant; Male; Maltose; Skin | 1975 |
Absence of acid maltase in glycogenesis type 2(Pompe's disease) in tissue culture.
Topics: Biopsy; Carbon Isotopes; Cardiomegaly; Culture Techniques; Female; Fibroblasts; Glucose; Glucosidases; Glycogen Storage Disease; Humans; Infant, Newborn; Maltose; Skin | 1969 |
Electrophoretic characterization of acidic and neutral amylo 1-4-glucosidase (acid maltase) in human tissues and evidence for two electrophoretic variants in acid maltase deficiency.
Topics: Amyloid; Cardiomegaly; Cells, Cultured; Child; Deficiency Diseases; Electrophoresis; Fibroblasts; Glucosidases; Glycogen Storage Disease; Heart Defects, Congenital; Heart Diseases; Humans; Hydrogen-Ion Concentration; Isoenzymes; Kidney; Leukocytes; Liver; Maltose; Muscles; Placenta; Skin | 1972 |
Rodent and human acid -glucosidase. Purification, properties and inhibition by antibodies. Investigation in type II glycogenosis.
Topics: Animals; Cardiomegaly; Chromatography, Gel; Cross Reactions; Female; Glucosidases; Glycogen; Glycogen Storage Disease; Heart Defects, Congenital; Heart Diseases; Humans; Hydrogen-Ion Concentration; Hydrolysis; Immunodiffusion; Immunoglobulins; Kinetics; Liver; Lysosomes; Maltose; Mice; Placenta; Pregnancy; Rabbits; Rats | 1972 |
Acid -glucosidase in amniotic fluid.
Topics: Amniotic Fluid; Carbon Isotopes; Cardiomegaly; Clinical Enzyme Tests; Disaccharides; Drug Stability; Embryonic and Fetal Development; Evaluation Studies as Topic; Female; Fibroblasts; Gestational Age; Glucosidases; Glycogen Storage Disease; Glycoside Hydrolases; Heart Defects, Congenital; Heart Diseases; Hot Temperature; Humans; Hydrogen-Ion Concentration; Lysosomes; Maltose; Nitrobenzenes; Potassium Chloride; Pregnancy | 1973 |
The role of lysosomes in the pathogeny of storage diseases.
Topics: Cardiomegaly; Cardiomyopathies; Cytoplasm; Glucosidases; Glycogen Storage Disease; Humans; Hydrogen-Ion Concentration; Liver; Lysosomes; Maltose; Metabolism, Inborn Errors; Microscopy, Electron | 1972 |
The subcellular distribution of enzymes in type II glycogenosis and the occurrence of an oligo-alpha-1,4-glucan glucohydrolase in human tissues.
Topics: Acid Phosphatase; Amylases; Chromatography, Paper; Glucose-6-Phosphatase; Glucosidases; Glucosyltransferases; Glycogen Storage Disease; Humans; In Vitro Techniques; Liver; Maltose; Oligosaccharides; Subcellular Fractions | 1965 |
Comparative study of acid maltase deficiency. Biochemical differences between infantile, childhood, and adult types.
Topics: Age Factors; Carbohydrate Metabolism, Inborn Errors; Child; Female; Glucosyltransferases; Glycogen Storage Disease; Glycoside Hydrolases; Humans; Hydrogen-Ion Concentration; Infant; Leukocytes; Liver; Male; Maltose; Metabolic Diseases; Middle Aged; Muscles; Myocardium | 1972 |
Adult acid maltase deficiency. Abnormalities in fibroblasts cultured from patients.
Topics: Adult; Age Factors; Cell Membrane; Cells, Cultured; Cytoplasm; Fascia; Fibroblasts; Glucosidases; Glycogen; Glycogen Storage Disease; Heart Diseases; Histocytochemistry; Humans; Hydrogen-Ion Concentration; Maltose; Microscopy, Electron; Middle Aged; Muscular Diseases; Skin | 1972 |
The use of leucocytes as an aid in the diagnosis of glycogen storage disease type II (Pompe's disease).
Topics: Antibodies; Antigen-Antibody Reactions; Cardiomyopathies; Glucosidases; Glycogen Storage Disease; Heterozygote; Humans; Hydrogen-Ion Concentration; Kinetics; Leukocytes; Liver; Lymphocytes; Maltose; Syndrome | 1974 |
The effect of disaccharides on the hyperlactacidaemia of glucose-6-phosphatase-deficient children.
Topics: Blood Glucose; Depression, Chemical; Female; Glycogen Storage Disease; Glycogen Storage Disease Type I; Humans; Infant; Lactates; Lactose; Maltose; Stimulation, Chemical; Sucrose; Time Factors | 1974 |
[Congenital disorders of carbohydrate metabolism in children].
Topics: Carbohydrate Metabolism, Inborn Errors; Child, Preschool; Female; Fructose; Galactosemias; Glycogen Storage Disease; Humans; Infant; Infant, Newborn; Lactose; Lactose Intolerance; Male; Maltose | 1965 |
Simultaneous absence of alpha-1,4-glucosidase and alpha-1,6-glucosidase activities (pH 4) in tissues of children with type II glycogen storage disease.
Topics: Autopsy; Biopsy; Child; Culture Techniques; Disaccharides; Drug Stability; Fibroblasts; Glucosidases; Glycogen; Glycogen Storage Disease; Glycoside Hydrolases; Glycosides; Humans; Hydrogen-Ion Concentration; Kinetics; Leukocytes; Liver; Lysosomes; Maltose; Muscles; Myocardium | 1970 |
The maltase, glucoamylase and transglucosylase activities of acid -glucosidase from rabbit muscle.
Topics: Animals; Binding Sites; Carbon Isotopes; Glucose; Glucosidases; Glucosyltransferases; Glycogen; Glycogen Storage Disease; Glycoside Hydrolases; Heart Diseases; Humans; Hydrogen-Ion Concentration; Kinetics; Maltose; Muscles; Polysaccharides; Rabbits; Sulfhydryl Reagents; Water | 1971 |