Page last updated: 2024-08-21

isovaleric acid and methylmalonic acid

isovaleric acid has been researched along with methylmalonic acid in 14 studies

Research

Studies (14)

TimeframeStudies, this research(%)All Research%
pre-19906 (42.86)18.7374
1990's3 (21.43)18.2507
2000's5 (35.71)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chalmers, RA; Hind, AJ; Iles, RA1
Algert, S; Kelts, DG; Nyhan, WL; Prodanos, C; Wolff, JA1
Guibaud, P; Rousson, R1
Charpentier, C; Coudé, FX; Depondt, E; Frézal, J; Mitchell, G; Munnich, A; Ogier, H; Rey, F; Rey, J; Saudubray, JM1
Chalmers, RA; Hoppel, CL; Roe, CR; Stacey, TE1
Briand, P; Cathelineau, L; Charpentier, C; Coudé, FX; Ogier, H; Saudubray, JM1
Bennett, MJ; Berry, GT; Hale, DE; Stanley, CA; Treem, WR; Willi, SM1
Hoppel, CL; Minkler, PE1
Chalmers, RA; Down, S; Halket, JM; Mallard, WG; Przyborowska, A; Stein, SE1
Blau, N; Bonafé, L; Burlina, AB; Chamoles, NA; Heizmann, CW; Kuster, T; Troxler, H1
Ogier de Baulny, H; Saudubray, JM1
Kim, KR; Lee, HJ; Paik, MJ1
Gao, XL; Gu, XF; Han, LS; Qiu, WJ; Ye, J1
Fuller, GG; Hsu, TT; Nishimura, S; Sonner, JM; Weng, Y; Zhao, J1

Reviews

1 review(s) available for isovaleric acid and methylmalonic acid

ArticleYear
Branched-chain organic acidurias.
    Seminars in neonatology : SN, 2002, Volume: 7, Issue:1

    Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids, Branched-Chain; Diagnosis, Differential; Glycine; Hemiterpenes; Humans; Infant, Newborn; Malonates; Maple Syrup Urine Disease; Methylmalonic Acid; Pentanoic Acids; Prognosis; Propionates

2002

Other Studies

13 other study(ies) available for isovaleric acid and methylmalonic acid

ArticleYear
Use of proton nuclear magnetic resonance spectroscopy in detection and study of organic acidurias.
    Clinical chemistry, 1985, Volume: 31, Issue:11

    Topics: Amino Acid Metabolism, Inborn Errors; Carboxylic Acids; Child, Preschool; Glutarates; Hemiterpenes; Humans; Magnetic Resonance Spectroscopy; Male; Maple Syrup Urine Disease; Methylmalonic Acid; Pentanoic Acids; Propionates; Protons

1985
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
Long term outcome of organic acidurias: survey of 105 French cases (1967-1983).
    Journal of inherited metabolic disease, 1984, Volume: 7 Suppl 1

    Topics: Acids; Adolescent; Child; Child, Preschool; France; Hemiterpenes; Humans; Infant; Infant, Newborn; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Methylmalonic Acid; Pentanoic Acids; Prognosis; Propionates; Time Factors

1984
Hudson memorial lecture. Neonatal management of organic acidurias. Clinical update.
    Journal of inherited metabolic disease, 1984, Volume: 7 Suppl 1

    Topics: Acids; Amino Acid Metabolism, Inborn Errors; Diuresis; Exchange Transfusion, Whole Blood; Hemiterpenes; Humans; Infant, Newborn; Maple Syrup Urine Disease; Methylmalonic Acid; Pentanoic Acids; Peritoneal Dialysis; Propionates

1984
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
Hyperammonemia secondary to hereditary organic acidurias: a study of 29 cases.
    Advances in experimental medicine and biology, 1982, Volume: 153

    Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Hemiterpenes; Humans; Infant, Newborn; Methylmalonic Acid; Pentanoic Acids; Propionates; Urea

1982
Renal handling of carnitine in secondary carnitine deficiency disorders.
    Pediatric research, 1993, Volume: 34, Issue:1

    Topics: Acyl Coenzyme A; Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenase, Long-Chain; Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Carnitine; Child; Child, Preschool; Female; Hemiterpenes; Humans; Infant; Kidney; Male; Methylmalonic Acid; Mitochondria; Oxidation-Reduction; Pentanoic Acids

1993
Quantification of carnitine and specific acylcarnitines by high-performance liquid chromatography: application to normal human urine and urine from patients with methylmalonic aciduria, isovaleric acidemia or medium-chain acyl-CoA dehydrogenase deficiency
    Journal of chromatography, 1993, Apr-02, Volume: 613, Issue:2

    Topics: Acetophenones; Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Amino Acid Metabolism, Inborn Errors; Carnitine; Child, Preschool; Chromatography, High Pressure Liquid; Female; Hemiterpenes; Humans; Indicators and Reagents; Infant; Methylmalonic Acid; Pentanoic Acids

1993
Deconvolution gas chromatography/mass spectrometry of urinary organic acids--potential for pattern recognition and automated identification of metabolic disorders.
    Rapid communications in mass spectrometry : RCM, 1999, Volume: 13, Issue:4

    Topics: Acyl-CoA Dehydrogenase; Autoanalysis; Child, Preschool; Dicarboxylic Acids; Fatty Acid Desaturases; Gas Chromatography-Mass Spectrometry; Glutarates; Hemiterpenes; Humans; Infant; Meglutol; Metabolism, Inborn Errors; Methylmalonic Acid; Pattern Recognition, Automated; Pentanoic Acids; Propionates

1999
Evaluation of urinary acylglycines by electrospray tandem mass spectrometry in mitochondrial energy metabolism defects and organic acidurias.
    Molecular genetics and metabolism, 2000, Volume: 69, Issue:4

    Topics: Acyl-CoA Dehydrogenase; Adolescent; Adult; Amidohydrolases; Biotinidase; Carbon-Nitrogen Ligases; Child; Child, Preschool; Fatty Acid Desaturases; Glycine; Hemiterpenes; Humans; Infant; Infant, Newborn; Mass Spectrometry; Meglutol; Metabolism, Inborn Errors; Methylmalonic Acid; Mitochondria; Pentanoic Acids; Propionates

2000
Simultaneous retention index analysis of urinary amino acids and carboxylic acids for graphic recognition of abnormal state.
    Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2005, Jul-05, Volume: 821, Issue:1

    Topics: Acetamides; Amino Acids; Carboxylic Acids; Child; Child, Preschool; Chromatography, Gas; Fluoroacetates; Hemiterpenes; Humans; Hydroxylamines; Infant; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Methylmalonic Acid; Organosilicon Compounds; Pentanoic Acids; Phenylketonurias; Trifluoroacetic Acid

2005
[Application of tandem mass spectrometry in diagnosis of organic acidemias].
    Zhonghua er ke za zhi = Chinese journal of pediatrics, 2005, Volume: 43, Issue:5

    Topics: Adolescent; Child; Child, Preschool; Female; Filtration; Gas Chromatography-Mass Spectrometry; Glutarates; Hemiterpenes; Humans; Infant; Male; Metabolism, Inborn Errors; Methylmalonic Acid; Pentanoic Acids; Propionic Acidemia; Tandem Mass Spectrometry

2005
Isovaleric, methylmalonic, and propionic acid decrease anesthetic EC50 in tadpoles, modulate glycine receptor function, and interact with the lipid 1,2-dipalmitoyl-Sn-glycero-3-phosphocholine.
    Anesthesia and analgesia, 2009, Volume: 108, Issue:5

    Topics: 1,2-Dipalmitoylphosphatidylcholine; Anesthetics, Inhalation; Animals; Cell Membrane; Chlorides; Dose-Response Relationship, Drug; Female; Hemiterpenes; Isoflurane; Larva; Membrane Potentials; Methylmalonic Acid; Mutation; Pentanoic Acids; Pressure; Propionates; Receptors, GABA-A; Receptors, Glycine; Surface Properties; Xenopus laevis

2009