phenyl acetate has been researched along with Lipid Metabolism, Inborn Error in 9 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 6 (66.67) | 18.7374 |
| 1990's | 1 (11.11) | 18.2507 |
| 2000's | 1 (11.11) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (11.11) | 2.80 |
| Authors | Studies |
|---|---|
| Banerji, T; DeBell, MJ; Hartley, MD; Kirkemo, LL; Scanlan, TS; Shokat, MD | 1 |
| Borba Rosa, R; da Costa Ferreira, G; Dutra-Filho, CS; Duval Wannmacher, CM; Maria, Rde C; Reis de Assis, D; Ribeiro, CA; Santos Perry, ML; Schuck, PF; Terezinha de Souza Wyse, A; Wajner, M | 1 |
| Coleman, RA; Grunfeld, C; Placezk, D; Williams, ML | 1 |
| Mapes, CA; Sweeley, CC | 1 |
| Den Tandt, WR; Giesberts, MA | 1 |
| Desnick, RJ; Krivit, W; Snyder, PD | 1 |
| Dacremont, G | 1 |
| de Groot, WP; Rietra, PJ; Tager, JM | 1 |
| Montreuil, J; Strecker, G | 1 |
9 other study(ies) available for phenyl acetate and Lipid Metabolism, Inborn Error
| Article | Year |
|---|---|
Pharmacological Complementation Remedies an Inborn Error of Lipid Metabolism.
Topics: Acetates; Adrenoleukodystrophy; Animals; ATP Binding Cassette Transporter, Subfamily D, Member 1; Disease Models, Animal; Fatty Acids; Female; Humans; Lipid Metabolism, Inborn Errors; Male; Mice; Mice, Knockout; Phenols; Prodrugs; Thyroid Hormones | 2020 |
Inhibition of energy metabolism in cerebral cortex of young rats by the medium-chain fatty acids accumulating in MCAD deficiency.
Topics: Acetates; Acyl-CoA Dehydrogenase; Age Factors; Animals; Antifungal Agents; Antihypertensive Agents; Caprylates; Carbon Radioisotopes; Cerebral Cortex; Citrate (si)-Synthase; Creatine Kinase; Decanoic Acids; Electron Transport; Energy Metabolism; Fatty Acids; Lipid Metabolism, Inborn Errors; Rats; Rats, Wistar | 2004 |
Neutral lipid storage disease: a possible functional defect in phospholipid- linked triacylglycerol metabolism.
Topics: Acetates; Cells, Cultured; Genes, Recessive; Glycolipids; Humans; In Vitro Techniques; Lipase; Lipid Metabolism, Inborn Errors; Male; Oleic Acid; Oleic Acids; Phospholipids; Plasmalogens; Triglycerides | 1991 |
Preparation and properties of an affinity column adsorbent for differentiation of multiple forms of -galactosidase activity.
Topics: Acetates; Adolescent; Amides; Aniline Compounds; Blood Chemical Analysis; Cerebrosides; Chromatography; Chromatography, Affinity; Chromatography, Thin Layer; Disaccharides; Electrophoresis; Female; Galactosidases; Glycolipids; Glycoproteins; Humans; Kidney; Lipid Metabolism, Inborn Errors; Male; Phosphatidylcholines; Polysaccharides; Staining and Labeling | 1973 |
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 |
The glycosphingolipids and glycosyl hydrolases of human blood platelets.
Topics: Acetates; Blood Platelets; Cerebrosides; Chromatography, Gas; Chromatography, Thin Layer; Fluorometry; Galactosidases; Gangliosides; Glucosidases; Glycolipids; Glycoside Hydrolases; Heterozygote; Hexosaminidases; Homozygote; Humans; Lipid Metabolism, Inborn Errors; Lipidoses | 1972 |
Ganglioside concentration in human plasma.
Topics: Acetates; Aging; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chromatography; Chromatography, Thin Layer; Cystic Fibrosis; Female; Gangliosides; Glycolipids; Humans; Infant; Intellectual Disability; Lipid Metabolism, Inborn Errors; Lipidoses; Male; Methods; Muscular Atrophy; Neuraminic Acids; Niemann-Pick Diseases; Sex Factors | 1972 |
Detection of Fabry hemizygotes and heterozygotes by measurement of -galactosidase in urine.
Topics: Acetates; Adolescent; Adult; Aged; Carrier State; Child; Child, Preschool; Circadian Rhythm; Dialysis; Drug Storage; Female; Galactosidases; Glycolipids; Heterozygote; Hexosaminidases; Homozygote; Humans; Infant; Lipid Metabolism, Inborn Errors; Male; Middle Aged | 1972 |
[Oligosaccharide excretion in a case of GM 2 gangliosidosis due to total N-acetylhexosaminidase deficiency].
Topics: Acetates; Carbohydrate Metabolism, Inborn Errors; Chemical Precipitation; Chromatography; Chromatography, Ion Exchange; Chromatography, Paper; Colorimetry; Ethanol; Fucose; Galactose; Gangliosides; Glucosamine; Glucose; Glycoproteins; Glycoside Hydrolases; Hexosamines; Hexosaminidases; Hexoses; Humans; Infant; Lipid Metabolism, Inborn Errors; Lipidoses; Mannose; Monosaccharides; Neuraminic Acids; Oligosaccharides; Uronic Acids | 1971 |