phenyl acetate has been researched along with Mucopolysaccharidoses in 6 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 5 (83.33) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (16.67) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Al-Saleh, S; Clarke, J; Gibbons, J; MacFarlane, J; MacLusky, I; Narang, I; Nashed, A; Riekstins, A | 1 |
Dorfman, A; Lamberg, SI | 1 |
Carrel, RE; Fluharty, AL; Kihara, H; Lassila, EL; Porter, MT; Trammell, J | 1 |
O'Brien, JS | 1 |
Bain, AD; Butterworth, J; McCrae, WM; Scott, F | 1 |
Den Tandt, WR; Giesberts, MA | 1 |
6 other study(ies) available for phenyl acetate and Mucopolysaccharidoses
Article | Year |
---|---|
Sleep-related breathing in children with mucopolysaccharidosis.
Topics: Acetates; Adolescent; Anti-Asthmatic Agents; Child; Child, Preschool; Cyclopropanes; Female; Humans; Infant; Male; Mucopolysaccharidoses; Polysomnography; Positive-Pressure Respiration; Prevalence; Quinolines; Respiration; Retrospective Studies; Sleep; Sleep Apnea Syndromes; Sulfides; Tonsillectomy; Treatment Outcome | 2009 |
Synthesis and degradation of hyaluronic acid in the cultured fibroblasts of Marfan's disease.
Topics: Acetates; Adult; Animals; Carbon Isotopes; Cattle; Cetylpyridinium; Cycloheximide; Female; Fibroblasts; Glucosamine; Glycosaminoglycans; Glycoside Hydrolases; Humans; Hyaluronic Acid; Kinetics; Male; Marfan Syndrome; Molecular Weight; Mucopolysaccharidoses; Staining and Labeling; Time Factors | 1973 |
Acid glycosidases in mucopolysaccharidoses fibroblasts.
Topics: Acetates; Carbohydrate Metabolism, Inborn Errors; Electrophoresis; Female; Fibroblasts; Fluorometry; Galactosidases; Glucosamine; Glucosephosphate Dehydrogenase; Glucuronidase; Glycosaminoglycans; Glycoside Hydrolases; Humans; Intellectual Disability; Male; Mucopolysaccharidoses; Retinitis Pigmentosa; Spectrophotometry | 1970 |
Sanfilippo syndrome: profound deficiency of alpha-acetylglucosaminidase activity in organs and skin fibroblasts from type-B patients.
Topics: Acetates; Amniotic Fluid; Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Female; Fibroblasts; Fucose; Glycosaminoglycans; Glycoside Hydrolases; Hexosaminidases; Humans; Intellectual Disability; Kidney; Liver; Male; Mucopolysaccharidoses; Pregnancy; Retinitis Pigmentosa; Skin | 1972 |
Lysosomal enzymes of cultured fibroblasts of cystic fibrosis patients.
Topics: Acetates; Acid Phosphatase; Arabinose; Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Child; Chondroitin; Cystic Fibrosis; Fibroblasts; Fucose; Galactosidases; Glucosidases; Glucuronidase; Glycosaminoglycans; Glycoside Hydrolases; Hexosaminidases; Humans; Lysosomes; Mannose; Mucopolysaccharidoses | 1972 |
Deficiency of lysosomal enzymes in storage diseases.
Topics: Acetates; Acid Phosphatase; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Female; Fucose; Galactosidases; Glucuronidase; Glycolipids; Glycosaminoglycans; Glycoside Hydrolases; Hexosaminidases; Humans; Hydrolases; Infant; Intellectual Disability; Leukocytes; Lipid Metabolism, Inborn Errors; Liver; Lysosomes; Male; Middle Aged; Mucopolysaccharidoses; Sulfatases | 1973 |