Page last updated: 2024-08-21

isovaleric acid and Deficiency Disease, Ornithine Carbamoyltransferase

isovaleric acid has been researched along with Deficiency Disease, Ornithine Carbamoyltransferase in 2 studies

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
Baykal, T; Demir, F; Demirkol, M; Huner, G1
Algert, S; Kelts, DG; Nyhan, WL; Prodanos, C; Wolff, JA1

Other Studies

2 other study(ies) available for isovaleric acid and Deficiency Disease, Ornithine Carbamoyltransferase

ArticleYear
Breastfeeding experience in inborn errors of metabolism other than phenylketonuria.
    Journal of inherited metabolic disease, 2005, Volume: 28, Issue:4

    Topics: Amino Acid Metabolism, Inborn Errors; Breast Feeding; Child, Preschool; Follow-Up Studies; Glutarates; Hemiterpenes; Humans; Infant; Infant Formula; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Methylmalonyl-CoA Mutase; Ornithine Carbamoyltransferase Deficiency Disease; Pentanoic Acids; Propionates; Time Factors

2005
Alanine decreases the protein requirements of infants with inborn errors of amino acid metabolism.
    Journal of neurogenetics, 1985, Volume: 2, Issue:1

    Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Amino Acids; Body Weight; Dietary Proteins; Female; Hemiterpenes; Humans; Infant; Male; Methylmalonic Acid; Ornithine Carbamoyltransferase Deficiency Disease; Pentanoic Acids; Propionates; Proteins

1985