Page last updated: 2024-08-24

hydracrylic acid and valerates

hydracrylic acid has been researched along with valerates in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19903 (42.86)18.7374
1990's0 (0.00)18.2507
2000's2 (28.57)29.6817
2010's2 (28.57)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Baker, H; Baswell, DL; Holman, RT; Mock, DM; Sweetman, L1
Green, A; Pollitt, RJ; Smith, R1
Sweetman, L1
Boylan, J; Cannon, MJ; Cederbaum, S; Cress, S; Jennings, ML; Mardach, R; Mock, DM; Roth, S; Wolf, B; Zempleni, J1
Yoon, HR1
Böhmer, D; Chandoga, J; Konkoľová, J; Kováčik, J; Kramarová, V; Paučinová, I; Repiský, M1
Afroze, B; Ali, ZZ; Fatimah, M; Jafri, L; Jamil, A; Khan, AH; Majid, H; Yusufzai, N1

Other Studies

7 other study(ies) available for hydracrylic acid and valerates

ArticleYear
Biotin deficiency complicating parenteral alimentation: diagnosis, metabolic repercussions, and treatment.
    The Journal of pediatrics, 1985, Volume: 106, Issue:5

    Topics: Alopecia; Biotin; Citrates; Diagnosis, Differential; Erythema; Fatty Acids, Essential; Female; Glycine; Humans; Infant; Isomerism; Lactates; Lactic Acid; Male; Nervous System Diseases; Parenteral Nutrition; Valerates; Zinc

1985
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
Two forms of biotin-responsive multiple carboxylase deficiency.
    Journal of inherited metabolic disease, 1981, Volume: 4, Issue:2

    Topics: Acute Disease; Biotin; Carbon-Carbon Ligases; Chronic Disease; Fibroblasts; Humans; Hydroxy Acids; Infant; Lactates; Lactic Acid; Ligases; Lymphocytes; Pyruvate Carboxylase Deficiency Disease; Valerates

1981
Biotin dependency due to a defect in biotin transport.
    The Journal of clinical investigation, 2002, Volume: 109, Issue:12

    Topics: Amidohydrolases; Biological Transport; Biotin; Biotinidase; Carbon-Carbon Ligases; Carboxy-Lyases; Carrier Proteins; Cell Line, Transformed; Child, Preschool; Female; Humans; Lactic Acid; Leukocytes, Mononuclear; Male; Membrane Glycoproteins; Methylmalonyl-CoA Decarboxylase; Pyruvate Carboxylase; Substance Withdrawal Syndrome; Symporters; Valerates

2002
Two step derivatization for the analyses of organic, amino acids and glycines on filter paper plasma by GC-MS/SIM.
    Archives of pharmacal research, 2007, Volume: 30, Issue:3

    Topics: Amino Acids; Blood Specimen Collection; Filtration; Gas Chromatography-Mass Spectrometry; Glycine; Humans; Infant; Infant, Newborn; Lactic Acid; Orotic Acid; Valerates

2007
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
Diagnostic dilemma of patients with methylmalonic aciduria: Experience from a tertiary care centre in Pakistan.
    JPMA. The Journal of the Pakistan Medical Association, 2018, Volume: 68, Issue:4

    Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Child, Preschool; Citrates; Cross-Sectional Studies; Female; Glycine; Humans; Infant; Lactic Acid; Male; Methionine; Mitochondrial Diseases; Pakistan; Tertiary Care Centers; Urinalysis; Valerates; Vitamin B 12 Deficiency

2018