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octanoyl-coenzyme a and Inborn Errors of Metabolism

octanoyl-coenzyme a has been researched along with Inborn Errors of Metabolism in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Izumi, T; Korematsu, S; Kosugi, Y; Kumamoto, T; Yamaguchi, S1
Hasegawa, Y; Hata, I; Kimura, M; Kobayashi, M; Nishimura, Y; Ono, H; Sakura, N; Shigematsu, Y; Tajima, G; Yamaguchi, S; Yofune, H1

Reviews

1 review(s) available for octanoyl-coenzyme a and Inborn Errors of Metabolism

ArticleYear
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.
    Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2005, Sep-05, Volume: 823, Issue:2

    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

Other Studies

1 other study(ies) available for octanoyl-coenzyme a and Inborn Errors of Metabolism

ArticleYear
Novel mutation of early, perinatal-onset, myopathic-type very-long-chain acyl-CoA dehydrogenase deficiency.
    Pediatric neurology, 2009, Volume: 41, Issue:2

    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