Compounds > 2-ethylhydracrylic acid
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2-ethylhydracrylic acid and Amino Acid Metabolism Disorders, Inborn

2-ethylhydracrylic acid has been researched along with Amino Acid Metabolism Disorders, Inborn in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19903 (60.00)18.7374
1990's0 (0.00)18.2507
2000's2 (40.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
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
Andresen, BS; Engel, K; Ensenauer, R; Häberle, J; Lehnert, W; Mégarbané, A; Reich, H; Röschinger, W; Sass, JO; Schirrmacher, O; Steuerwald, U; Zschocke, J1
Jakobs, C; Nyhan, WL; Sweetman, L1
Green, A; Pollitt, RJ; Smith, R1
Mamer, OA; Tjoa, SS1

Other Studies

5 other study(ies) available for 2-ethylhydracrylic acid and Amino Acid Metabolism Disorders, Inborn

ArticleYear
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
2-Methylbutyryl-coenzyme A dehydrogenase deficiency: functional and molecular studies on a defect in isoleucine catabolism.
    Molecular genetics and metabolism, 2008, Volume: 93, Issue:1

    Topics: Amino Acid Metabolism, Inborn Errors; Butyryl-CoA Dehydrogenase; Cells, Cultured; Child; Child, Preschool; Female; Genotype; Glycine; Humans; Infant; Isoleucine; Male; Metabolism; Valerates

2008
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
Excessive excretion of beta-alanine and of 3-hydroxypropionic, R- and S-3-aminoisobutyric, R- and S-3-hydroxyisobutyric and S-2-(hydroxymethyl)butyric acids probably due to a defect in the metabolism of the corresponding malonic semialdehydes.
    Journal of inherited metabolic disease, 1985, Volume: 8, Issue:2

    Topics: Alanine; Aldehyde Oxidoreductases; Amino Acid Metabolism, Inborn Errors; Aminoisobutyric Acids; beta-Alanine; Child, Preschool; Humans; Hydroxybutyrates; Lactates; Lactic Acid; Male; Malonate-Semialdehyde Dehydrogenase (Acetylating); Malonates; Malondialdehyde; Methylmalonate-Semialdehyde Dehydrogenase (Acylating); Valerates

1985
2-Ethylhydracrylic acid: a newly described urinary organic acid.
    Clinica chimica acta; international journal of clinical chemistry, 1974, Sep-16, Volume: 55, Issue:2

    Topics: Acyltransferases; Amino Acid Metabolism, Inborn Errors; Chromatography, Gas; Coenzyme A; Humans; Hydroxy Acids; Hydroxybutyrates; Isoleucine; Keto Acids; Malonates; Mass Spectrometry; Valerates

1974