octanoylcarnitine has been researched along with Inborn Errors of Metabolism in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (25.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (50.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Adams, DJ; Arnold, GL; Caggana, M; Devincentis, E; Erbe, R; Galvin-Parton, PA; Kronn, D; Levy, PA; Mofidi, S; Nichols, M; Pellegrino, JE; Saavedra-Matiz, CA; Wasserstein, M | 1 |
| Lehotay, DC; LePage, J; Rockman-Greenberg, C; Thompson, JR | 1 |
| Baumgartner, C; Baumgartner, D | 1 |
| Maltby, DA; Millington, DS; Roe, CR; Wellman, RB | 1 |
4 other study(ies) available for octanoylcarnitine and Inborn Errors of Metabolism
| Article | Year |
|---|---|
Lack of genotype-phenotype correlations and outcome in MCAD deficiency diagnosed by newborn screening in New York State.
Topics: Acyl-CoA Dehydrogenases; Carnitine; Fatty Acids; Female; Genotype; Humans; Infant, Newborn; Male; Metabolism, Inborn Errors; Mutation; Neonatal Screening; New York; Phenotype; Prognosis | 2010 |
Blood acylcarnitine levels in normal newborns and heterozygotes for medium-chain acyl-CoA dehydrogenase deficiency: a relationship between genotype and biochemical phenotype?
Topics: Acyl-CoA Dehydrogenase; Adenine; Carnitine; Diagnosis, Differential; Gene Frequency; Genotype; Guanine; Heterozygote; Humans; Infant, Low Birth Weight; Infant, Newborn; Metabolism, Inborn Errors; Osmolar Concentration; Phenotype | 2004 |
Biomarker discovery, disease classification, and similarity query processing on high-throughput MS/MS data of inborn errors of metabolism.
Topics: Acyl-CoA Dehydrogenase; Biomarkers; Carnitine; Case-Control Studies; Humans; Mass Spectrometry; Metabolism, Inborn Errors; Methylmalonic Acid | 2006 |
Post-mortem recognition of inherited metabolic disorders from specific acylcarnitines in tissue in cases of sudden infant death.
Topics: Acyl-CoA Dehydrogenase; Carnitine; Fatty Acid Desaturases; Female; Humans; Infant; Infant, Newborn; Male; Metabolism, Inborn Errors; Sudden Infant Death | 1987 |