n-caproylglycine has been researched along with caprylates in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (50.00) | 18.7374 |
| 1990's | 1 (25.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| David, M; Divry, P; Gregersen, N; Hobolth, N; Kølvraa, S; Mortensen, PB; Rasmussen, K | 1 |
| Gregersen, N; Hobolth, N; Kølvraa, S; Lauritzen, R; Rasmussen, K; Rosleff, F | 1 |
| Bennett, MJ; Ostfeld, RJ; Ragni, MC; Santer, R; Schmidt-Sommerfeld, E | 1 |
| Albers, S; Irons, M; Levy, HL; Marsden, D; Strauss, AW | 1 |
4 other study(ies) available for n-caproylglycine and caprylates
| Article | Year |
|---|---|
General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three cases.
Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Adipates; Caproates; Caprylates; Carboxylic Acids; Child, Preschool; Decanoic Acids; Dicarboxylic Acids; Female; Glycine; Humans; Hydroxy Acids; Hydroxybutyrates; Infant; Male | 1983 |
Non-ketotic C6-C10-dicarboxylic aciduria: biochemical investigations of two cases.
Topics: Adipates; Caproates; Caprylates; Child, Preschool; Chromatography, Gas; Decanoic Acids; Dicarboxylic Acids; Fatty Acid Desaturases; Fatty Acids; Glycine; Humans; Hydroxy Acids; Hydroxybutyrates; Hypoglycemia; Infant; Lipid Metabolism, Inborn Errors; Male; Mass Spectrometry; Valerates | 1980 |
Population screening for medium-chain acyl-CoA dehydrogenase deficiency: analysis of medium-chain fatty acids and acylglycines in blood spots.
Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Caprylates; Child, Preschool; Decanoic Acids; Fatty Acids; Fatty Acids, Monounsaturated; Gas Chromatography-Mass Spectrometry; Glycine; Humans; Infant; Infant, Newborn; Neonatal Screening; Reference Values; Sensitivity and Specificity | 1994 |
Compound heterozygosity in four asymptomatic siblings with medium-chain acyl-CoA dehydrogenase deficiency.
Topics: Acyl-CoA Dehydrogenases; Caprylates; Carnitine; Child; Child, Preschool; Dicarboxylic Acids; DNA Mutational Analysis; Female; Glycine; Heterozygote; Humans; Infant, Newborn; Male; Mutation; Neonatal Screening | 2001 |