Page last updated: 2024-08-21

isovaleric acid and 3-methylbutyrylcarnitine

isovaleric acid has been researched along with 3-methylbutyrylcarnitine in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19902 (28.57)18.7374
1990's4 (57.14)18.2507
2000's0 (0.00)29.6817
2010's1 (14.29)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Dan, M; Fujioka, M; Kanaoka, H; Kikawa, Y; Shigematsu, Y; Sudo, M1
Chalmers, RA; Hoppel, CL; Roe, CR; Stacey, TE1
Bohan, TP; Kahler, SG; Maltby, DA; Millington, DS; Roe, CR1
Barbato, R; Burlina, AB; De Tullio, R; Di Lisa, F; Menabŏ, R; Salamino, F; Siliprandi, N1
Fries, MH; Jurecki, E; Packman, S; Rinaldo, P; Schmidt-Sommerfeld, E1
Abdenur, JE; Chamoles, NA; Fuertes, AN; Guinle, AE; Schenone, AB1
Aldamiz-Echevarría, L; Barros, P; Belanger-Quintana, A; Blasco, J; Bueno, MA; Couce, ML; Fernández-Marmiesse, A; García-Silva, MT; Márquez-Armenteros, AM; Navarrete, R; Pérez, B; Pérez-Cerdá, C; Vitoria, I; Vives, I1

Other Studies

7 other study(ies) available for isovaleric acid and 3-methylbutyrylcarnitine

ArticleYear
Prenatal diagnosis of isovaleric acidemia by fast atom bombardment and tandem mass spectrometry.
    Clinica chimica acta; international journal of clinical chemistry, 1991, Dec-16, Volume: 203, Issue:2-3

    Topics: Amniotic Fluid; Carnitine; Female; Fetal Diseases; Glycine; Hemiterpenes; Humans; Isovaleryl-CoA Dehydrogenase; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Pentanoic Acids; Pregnancy; Prenatal Diagnosis; Spectrometry, Mass, Fast Atom Bombardment

1991
Urinary excretion of l-carnitine and acylcarnitines by patients with disorders of organic acid metabolism: evidence for secondary insufficiency of l-carnitine.
    Pediatric research, 1984, Volume: 18, Issue:12

    Topics: Acyl-CoA Dehydrogenases; Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids, Branched-Chain; Carnitine; Child; Child, Preschool; Female; Hemiterpenes; Humans; Infant; Infant, Newborn; Lysine; Male; Methylmalonic Acid; Middle Aged; Pentanoic Acids; Propionates

1984
L-carnitine therapy in isovaleric acidemia.
    The Journal of clinical investigation, 1984, Volume: 74, Issue:6

    Topics: Amino Acid Metabolism, Inborn Errors; Carnitine; Child, Preschool; Chromatography, Ion Exchange; Glycine; Hemiterpenes; Humans; Isovaleryl-CoA Dehydrogenase; Male; Mass Spectrometry; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Pentanoic Acids; Valerates

1984
Involvement of erythrocyte calpain in glycine- and carnitine-treated isovaleric acidemia.
    Pediatric research, 1994, Volume: 36, Issue:2

    Topics: Calpain; Carnitine; Child; Erythrocytes; Female; Glycine; Hemiterpenes; Humans; Isovaleryl-CoA Dehydrogenase; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Pentanoic Acids

1994
Isovaleric acidemia: response to a leucine load after three weeks of supplementation with glycine, L-carnitine, and combined glycine-carnitine therapy.
    The Journal of pediatrics, 1996, Volume: 129, Issue:3

    Topics: Amino Acid Metabolism, Inborn Errors; Carnitine; Child; Female; Glycine; Hemiterpenes; Humans; Isovaleryl-CoA Dehydrogenase; Leucine; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Pentanoic Acids

1996
Diagnosis of isovaleric acidaemia by tandem mass spectrometry: false positive result due to pivaloylcarnitine in a newborn screening programme.
    Journal of inherited metabolic disease, 1998, Volume: 21, Issue:6

    Topics: Carnitine; False Positive Reactions; Female; Gas Chromatography-Mass Spectrometry; Hemiterpenes; Humans; Infant, Newborn; Mass Spectrometry; Metabolism, Inborn Errors; Neonatal Screening; Pentanoic Acids; Sulbactam; Urinary Tract Infections

1998
Genotype and phenotype characterization in a Spanish cohort with isovaleric acidemia.
    Journal of human genetics, 2017, Volume: 62, Issue:3

    Topics: Acute Disease; Amino Acid Metabolism, Inborn Errors; Asymptomatic Diseases; Carnitine; Child; Child, Preschool; Chronic Disease; Creatinine; Female; Fibroblasts; Gene Expression; Genetic Association Studies; Genotype; Glycine; Hemiterpenes; Humans; Infant; Infant, Newborn; Isovaleryl-CoA Dehydrogenase; Male; Mutation; Neonatal Screening; Pentanoic Acids; Phenotype; Prevalence; Spain

2017