Page last updated: 2024-09-05

2-ethylhydracrylic acid and alpha-methyl-beta-hydroxybutyrate

2-ethylhydracrylic acid has been researched along with alpha-methyl-beta-hydroxybutyrate in 2 studies

Compound Research Comparison

Studies
(2-ethylhydracrylic acid)
Trials
(2-ethylhydracrylic acid)
Recent Studies (post-2010)
(2-ethylhydracrylic acid)
Studies
(alpha-methyl-beta-hydroxybutyrate)
Trials
(alpha-methyl-beta-hydroxybutyrate)
Recent Studies (post-2010) (alpha-methyl-beta-hydroxybutyrate)
12032305

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19901 (50.00)18.7374
1990's0 (0.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Jakobs, C; Nyhan, WL; Sweetman, L1
Baldellou, A; Briones, P; Campistol, J; Cortés, N; Delpiccolo, C; Fernández, C; Fons, C; Fuentes-Castelló, MA; García-Villoria, J; González, I; Hernández-Gonzalez, A; Messeguer, A; Navarro-Sastre, A; Pérez-Cerdá, C; Ribes, A1

Other Studies

2 other study(ies) available for 2-ethylhydracrylic acid and alpha-methyl-beta-hydroxybutyrate

ArticleYear
Hydroxy acid metabolites of branched-chain amino acids in amniotic fluid.
    Clinica chimica acta; international journal of clinical chemistry, 1984, Jul-16, Volume: 140, Issue:2

    Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids, Branched-Chain; Amniotic Fluid; Caproates; Female; Gas Chromatography-Mass Spectrometry; Humans; Hydroxy Acids; Hydroxybutyrates; Maple Syrup Urine Disease; Methylmalonic Acid; Pentanoic Acids; Pregnancy; Prenatal Diagnosis; Valerates

1984
Study of patients and carriers with 2-methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency: difficulties in the diagnosis.
    Clinical biochemistry, 2009, Volume: 42, Issue:1-2

    Topics: 3-Hydroxyacyl CoA Dehydrogenases; Alcohol Oxidoreductases; Amino Acid Metabolism, Inborn Errors; Female; Glycine; Heredodegenerative Disorders, Nervous System; Humans; Hydroxybutyrates; Infant; Infant, Newborn; Male; Valerates

2009