glycogen has been researched along with Mucopolysaccharidoses* in 6 studies
3 review(s) available for glycogen and Mucopolysaccharidoses
| Article | Year |
|---|---|
Urinary amino acid glycosides and oligosaccharides in health and disease.
Due to heterogeneity and lack of suitable fractionation techniques it is only recently that more detailed information about urinary low molecular weight carbohydrates has been obtained. Ingemar Berggård was one of the pioneers who opened up this field and outlined the directions towards fruitful progress. Today more than one hundred well characterized oligosaccharides and amino acid glycosides have been described. This review covers the latest development and discusses the mechanisms behind the urinary excretion. Topics: Blood Group Antigens; Female; Glycogen; Glycopeptides; Glycoproteins; Humans; Lactation; Mucopolysaccharidoses; Oligosaccharides; Pregnancy; Pregnancy Proteins | 1980 |
[Hereditary diseases connected with defective metabolism of polysaccharides and mixed carbohydrate-containing biopolymers].
Topics: Amniocentesis; Animals; Carbohydrate Metabolism, Inborn Errors; Cats; Cattle; Disease Models, Animal; Dogs; Female; Glycogen; Glycogen Storage Disease; Glycolipids; Glycoproteins; Humans; Male; Mucopolysaccharidoses; Polysaccharides; Pregnancy; Prenatal Diagnosis; Rats | 1973 |
Degenerative disease of the central nervous system.
Topics: Angiokeratoma; Arthritis; Autopsy; Biopsy; Carbohydrate Metabolism, Inborn Errors; Central Nervous System Diseases; Child; Diffuse Cerebral Sclerosis of Schilder; Encephalitis; Encephalomyelitis; Gangliosides; Gaucher Disease; Glycogen; Glycosaminoglycans; Humans; Lipid Metabolism; Lipidoses; Medical History Taking; Metabolic Diseases; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Multiple Sclerosis; Myelin Sheath; Nerve Degeneration; Neurons; Niemann-Pick Diseases; Retinal Degeneration; Slow Virus Diseases; Virus Diseases | 1969 |
3 other study(ies) available for glycogen and Mucopolysaccharidoses
| Article | Year |
|---|---|
Fine structure and silver-staining patterns of lysosome-like bodies in absorptive cells of the small intestine in normal children and children with a lysosomal storage disease.
Topics: Adolescent; Biopsy; Child; Child, Preschool; Female; Gangliosides; Glycogen; Glycogen Storage Disease; Golgi Apparatus; Humans; Infant; Intellectual Disability; Intestine, Small; Leukocytes; Lipid Metabolism, Inborn Errors; Lysosomes; Macrophages; Male; Microscopy, Electron; Mucopolysaccharidoses | 1973 |
Colorimetric measurement of dermatan sulphate.
The periodate-Schiff reaction has been adapted for the measurement of dermatan sulphate. The method is specific for this glycosaminoglycan, provided that glycogen and glycoproteins are removed. Measurements of dermatan sulphate present in the urine of patients affected by various mucopolysaccharidoses indicate a good agreement between the values obtained with enzymic methods and those obtained with the colorimetric method described. Topics: Chromatography; Colorimetry; Glycogen; Glycoproteins; Glycosaminoglycans; Humans; Methods; Mucopolysaccharidoses; Periodic Acid; Staining and Labeling | 1971 |
Fine-needle aspiration biopsy of human liver for enzymatic diagnosis of glycogen storage disease and gargoylism.
Topics: Adult; Biopsy; Child; Child, Preschool; Diagnosis, Differential; Female; Galactosidases; Glucose-6-Phosphatase; Glucosidases; Glucosyltransferases; Glucuronidase; Glycogen; Glycogen Storage Disease; Glycoside Hydrolases; Hepatomegaly; Humans; Infant; Liver; Liver Function Tests; Male; Methods; Mucopolysaccharidoses | 1970 |