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3-methylglutaconic acid and Lipid Metabolism, Inborn Error

3-methylglutaconic acid has been researched along with Lipid Metabolism, Inborn Error in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (50.00)18.2507
2000's0 (0.00)29.6817
2010's1 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Antonetti, G; Boenzi, S; Carrozzo, R; Catesini, G; Diodato, D; Dionisi-Vici, C; Martinelli, D; Olivieri, G; Rizzo, C; Sacchetti, E; Semeraro, M1
Kelley, RI; Kratz, L1

Other Studies

2 other study(ies) available for 3-methylglutaconic acid and Lipid Metabolism, Inborn Error

ArticleYear
The urinary organic acids profile in single large-scale mitochondrial DNA deletion disorders.
    Clinica chimica acta; international journal of clinical chemistry, 2018, Volume: 481

    Topics: 3-Hydroxybutyric Acid; Acyl-CoA Dehydrogenase, Long-Chain; Adolescent; Child; Child, Preschool; Congenital Bone Marrow Failure Syndromes; DNA, Mitochondrial; Fumarates; Glutarates; Humans; Hydroxybutyrates; Infant; Kearns-Sayre Syndrome; Lactic Acid; Lipid Metabolism, Inborn Errors; Mitochondrial Diseases; Muscular Diseases; Pyruvic Acid; Retrospective Studies; Valerates

2018
3-methylglutaconic acidemia in Smith-Lemli-Opitz syndrome.
    Pediatric research, 1995, Volume: 37, Issue:5

    Topics: Adolescent; Child; Cholesterol; Dehydrocholesterols; Glutarates; Humans; Lipid Metabolism, Inborn Errors; Syndrome

1995