Page last updated: 2024-08-21

isovaleric acid and BH4 Deficiency

isovaleric acid has been researched along with BH4 Deficiency in 5 studies

Research

Studies (5)

Timeframe	Studies, this research(%)	All Research%
pre-1990	2 (40.00)	18.7374
1990's	1 (20.00)	18.2507
2000's	2 (40.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Kim, KR; Lee, HJ; Paik, MJ	1
Bal, D; Gradowska, W; Gryff-Keller, A; Kraska-Dziadecka, A	1
Desnick, RJ; Schweitzer, LB	1
Burke, DG; Danks, D; Halpern, B; Malegan, D; McCairns, E; Schlesinger, P; Wilken, B	1
Liammongkolkul, S; Naylor, EW; Wasant, P	1

Reviews

1 review(s) available for isovaleric acid and BH4 Deficiency

Article	Year
Inherited metabolic diseases: advances in delineation, diagnosis, and treatment. Birth defects original article series, 1983, Volume: 19, Issue:5 Topics: Argininosuccinic Aciduria; Bone Marrow Transplantation; Carboxy-Lyases; Cystinosis; Genetic Engineering; Hemiterpenes; Humans; Infant; Infant, Newborn; Metabolism, Inborn Errors; Mucolipidoses; Mucopolysaccharidoses; Mucopolysaccharidosis III; Pentanoic Acids; Phenylketonurias; Thalassemia	1983

Article

Year

Inherited metabolic diseases: advances in delineation, diagnosis, and treatment.

Birth defects original article series, 1983, Volume: 19, Issue:5

Topics: Argininosuccinic Aciduria; Bone Marrow Transplantation; Carboxy-Lyases; Cystinosis; Genetic Engineering; Hemiterpenes; Humans; Infant; Infant, Newborn; Metabolism, Inborn Errors; Mucolipidoses; Mucopolysaccharidoses; Mucopolysaccharidosis III; Pentanoic Acids; Phenylketonurias; Thalassemia

1983

Other Studies

4 other study(ies) available for isovaleric acid and BH4 Deficiency

Article	Year
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
Investigation of a wide spectrum of inherited metabolic disorders by 13C NMR spectroscopy. Acta biochimica Polonica, 2008, Volume: 55, Issue:1 Topics: Biomarkers; Canavan Disease; Glutarates; Hemiterpenes; Humans; Lactic Acid; Magnetic Resonance Spectroscopy; Metabolic Diseases; Models, Chemical; Orotic Acid; Pentanoic Acids; Phenylketonurias; Pyrrolidonecarboxylic Acid; Tyrosinemias; Urinalysis	2008
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