Compounds > 3-hydroxyisobutyric acid

3-hydroxyisobutyric acid and lactic acid

3-hydroxyisobutyric acid has been researched along with lactic acid in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19903 (75.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Green, A; Pollitt, RJ; Smith, R1
Bankier, A; Barnes, G; Blakey, J; Brown, G; Haan, E; Hunt, S; Mitchell, D1
Congdon, PJ; Green, A; Haigh, D; Pollitt, RJ; Smith, R1
Böhmer, D; Chandoga, J; Konkoľová, J; Kováčik, J; Kramarová, V; Paučinová, I; Repiský, M1

Other Studies

4 other study(ies) available for 3-hydroxyisobutyric acid and lactic acid

ArticleYear
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
Severe illness caused by the products of bacterial metabolism in a child with a short gut.
    European journal of pediatrics, 1985, Volume: 144, Issue:1

    Topics: Acidosis; Caproates; Child; Cognition Disorders; Consciousness Disorders; Humans; Hydroxybutyrates; Lactates; Lactic Acid; Malabsorption Syndromes; Male; Phenylacetates; Phenylpropionates; Short Bowel Syndrome

1985
Hypermethioninaemia and 3-hydroxyisobutyric aciduria in an apparently healthy baby.
    Journal of inherited metabolic disease, 1981, Volume: 4, Issue:2

    Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Aminoisobutyric Acids; Humans; Hydroxybutyrates; Infant; Isomerism; Lactates; Lactic Acid; Methionine; Thymine; Valine

1981
Severe child form of primary hyperoxaluria type 2 - a case report revealing consequence of GRHPR deficiency on metabolism.
    BMC medical genetics, 2017, 05-31, Volume: 18, Issue:1

    Topics: Alcohol Oxidoreductases; Aminoisobutyric Acids; DNA Mutational Analysis; Female; Gas Chromatography-Mass Spectrometry; Humans; Hydroxybutyrates; Hyperoxaluria, Primary; Infant; Lactic Acid; Urolithiasis; Valerates

2017