hyaluronoglucosaminidase has been researched along with Deficiency, Mental in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 8 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Lamberg, SI; Stoolmiller, AC | 1 |
| Józsa, L; Szabó, L | 2 |
| Koch, F; Platt, D | 1 |
| Bachhawat, BK; George, E | 1 |
| Gordon, BA; Haust, MD | 1 |
| Feleki, V; Gordon, BA | 1 |
| Harvey, J; Robertson, WV | 1 |
1 review(s) available for hyaluronoglucosaminidase and Deficiency, Mental
| Article | Year |
|---|---|
Glycosaminoglycans. A biochemical and clinical review.
Topics: Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Chondroitin; Cornea; Corneal Opacity; Dermatan Sulfate; Fibroblasts; Galactose; Glucosamine; Glycosaminoglycans; Heparin; Humans; Hyaluronic Acid; Hyaluronoglucosaminidase; Intellectual Disability; Male; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Proteoglycans; Retinitis Pigmentosa; Skin; Staining and Labeling; Sulfatases; Testis | 1974 |
7 other study(ies) available for hyaluronoglucosaminidase and Deficiency, Mental
| Article | Year |
|---|---|
Urinary hyaluronidase activity in mucopolysaccharidosis.
Topics: Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Female; Glycosaminoglycans; Humans; Hyaluronoglucosaminidase; Infant; Intellectual Disability; Male; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Retinitis Pigmentosa | 1969 |
[Increase of the serum activity of hyaluronidase, beta glucuronidase and beta acetylglucosaminidase in mucopolysaccharidoses].
Topics: Carbohydrate Metabolism, Inborn Errors; Glucuronidase; Glycosaminoglycans; Glycoside Hydrolases; Humans; Hyaluronoglucosaminidase; Intellectual Disability; Methods; Mucopolysaccharidosis IV | 1969 |
Brain glycosaminoglycans and glycosaminoglycan sulphotransferase in Sanfilippo syndrome.
Topics: Biopsy; Brain Chemistry; Carbohydrate Metabolism, Inborn Errors; Child; Chondroitin; Glycosaminoglycans; Heparin; Humans; Hyaluronoglucosaminidase; Intellectual Disability; Male; Sulfates; Sulfur Isotopes; Transferases | 1970 |
The mucopolysaccharidoses types I, II, and 3: urinary findings in 23 cases.
Topics: Adolescent; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chromatography, Gas; Chromatography, Gel; Chromatography, Ion Exchange; Female; Galactosamine; Glucosamine; Glycosaminoglycans; Hexosamines; Humans; Hyaluronoglucosaminidase; Infant; Intellectual Disability; Male; Mucopolysaccharidosis I; Mucopolysaccharidosis II; Retinitis Pigmentosa; Sulfates; Testis; Uronic Acids | 1970 |
Acid hydrolases in the serum and liver in mucopolysaccharidoses types I and 3.
Topics: Acid Phosphatase; Adolescent; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Fucose; Galactosidases; Glucuronidase; Glycosaminoglycans; Glycoside Hydrolases; Hexosaminidases; Humans; Hyaluronoglucosaminidase; Intellectual Disability; Liver; Mannose; Mucopolysaccharidosis I; Sulfatases | 1970 |
The determination of galactose in urinary acidic glycosaminoglycans as a measure of keratan sulfate-like substances in urine.
Topics: Achondroplasia; Adolescent; Adult; Aged; Aging; Arthritis, Rheumatoid; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chromatography, Ion Exchange; Chromatography, Thin Layer; Colorimetry; Dermatomyositis; Female; Galactose; Glucosamine; Glycosaminoglycans; Humans; Hyaluronoglucosaminidase; Infant; Infant, Newborn; Intellectual Disability; Lipid Metabolism, Inborn Errors; Male; Methods; Middle Aged; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Retinitis Pigmentosa; Sulfuric Acids | 1972 |
Determination of heterozygous carrier state from the urine of the parents of children suffering from mucopolysaccharidosis.
Topics: Adult; Carbohydrate Metabolism, Inborn Errors; Child; Female; Glycosaminoglycans; Heterozygote; Humans; Hyaluronoglucosaminidase; Intellectual Disability; Male; Mucopolysaccharidoses | 1972 |