octanoyl-coenzyme a has been researched along with Metabolism, Inborn Errors in 2 studies
*Metabolism, Inborn Errors: Errors in metabolic processes resulting from inborn genetic mutations that are inherited or acquired in utero. [MeSH]
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Izumi, T; Korematsu, S; Kosugi, Y; Kumamoto, T; Yamaguchi, S | 1 |
| Hasegawa, Y; Hata, I; Kimura, M; Kobayashi, M; Nishimura, Y; Ono, H; Sakura, N; Shigematsu, Y; Tajima, G; Yamaguchi, S; Yofune, H | 1 |
1 review(s) available for octanoyl-coenzyme a and Metabolism, Inborn Errors
| Article | Year |
|---|---|
Enzymatic diagnosis of medium-chain acyl-CoA dehydrogenase deficiency by detecting 2-octenoyl-CoA production using high-performance liquid chromatography: a practical confirmatory test for tandem mass spectrometry newborn screening in Japan.
Topics: Acyl Coenzyme A; Acyl-CoA Dehydrogenase; Base Sequence; Child, Preschool; Chromatography, High Pressure Liquid; Female; Ferrous Compounds; Humans; Infant; Infant, Newborn; Japan; Lymphocytes; Male; Metabolism, Inborn Errors; Neonatal Screening; Reproducibility of Results; Sequence Deletion; Sequence Homology, Nucleic Acid; Spectrometry, Mass, Electrospray Ionization | 2005 |
1 other study(ies) available for octanoyl-coenzyme a and Metabolism, Inborn Errors
| Article | Year |
|---|---|
Novel mutation of early, perinatal-onset, myopathic-type very-long-chain acyl-CoA dehydrogenase deficiency.
Topics: Acyl Coenzyme A; Acyl-CoA Dehydrogenase, Long-Chain; Age of Onset; Carnitine; DNA Mutational Analysis; Fibroblasts; Humans; Infant, Newborn; Male; Metabolism, Inborn Errors; Muscles; Mutation; Palmitoyl Coenzyme A; Rhabdomyolysis; Skin; Treatment Outcome | 2009 |