Page last updated: 2024-08-21

isovaleric acid and BCKD Deficiency

isovaleric acid has been researched along with BCKD Deficiency in 9 studies

Research

Studies (9)

TimeframeStudies, this research(%)All Research%
pre-19905 (55.56)18.7374
1990's1 (11.11)18.2507
2000's3 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Kim, KR; Lee, HJ; Paik, MJ1
Baykal, T; Demir, F; Demirkol, M; Huner, G1
Guibaud, P; Rousson, R1
Charpentier, C; Coudé, FX; Depondt, E; Frézal, J; Mitchell, G; Munnich, A; Ogier, H; Rey, F; Rey, J; Saudubray, JM1
Burke, DG; Danks, D; Halpern, B; Malegan, D; McCairns, E; Schlesinger, P; Wilken, B1
Liammongkolkul, S; Naylor, EW; Wasant, P1
Ogier de Baulny, H; Saudubray, JM1
Chalmers, RA; Hind, AJ; Iles, RA1
Josephson, MW; Oliphant, C; Tsai, MY1

Reviews

1 review(s) available for isovaleric acid and BCKD Deficiency

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

8 other study(ies) available for isovaleric acid and BCKD Deficiency

ArticleYear
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
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
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
Profiles of urinary volatiles from metabolic disorders characterized by unusual odors.
    Clinical chemistry, 1983, Volume: 29, Issue:10

    Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Chromatography, Gas; Flame Ionization; Hemiterpenes; Humans; Infant, Newborn; Maple Syrup Urine Disease; Methylamines; Pentanoic Acids; Phenylketonurias; Valerates

1983
Detection of inherited metabolic disorders via tandem mass spectrometry in Thai infants.
    The Southeast Asian journal of tropical medicine and public health, 1999, Volume: 30 Suppl 2

    Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Blood Chemical Analysis; Carnitine Acyltransferases; Child; Fatty Acids; Hemiterpenes; Humans; Infant; Infant, Newborn; Male; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Pentanoic Acids; Phenylketonurias; Retrospective Studies; Spectrometry, Mass, Electrospray Ionization; Thailand

1999
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
Identification of metabolites diagnostic for organic acidurias by simultaneous dual-column capillary gas chromatography.
    Journal of chromatography, 1985, May-31, Volume: 341, Issue:1

    Topics: Acidosis; Chromatography, Gas; Gas Chromatography-Mass Spectrometry; Hemiterpenes; Humans; Indicators and Reagents; Maple Syrup Urine Disease; Pentanoic Acids; Propionates

1985