Page last updated: 2024-09-05

butyrylcarnitine and ethylmalonic acid

butyrylcarnitine has been researched along with ethylmalonic acid in 6 studies

Compound Research Comparison

Studies
(butyrylcarnitine)
Trials
(butyrylcarnitine)
Recent Studies (post-2010)
(butyrylcarnitine)
Studies
(ethylmalonic acid)
Trials
(ethylmalonic acid)
Recent Studies (post-2010) (ethylmalonic acid)
29213101224

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's4 (66.67)29.6817
2010's2 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bali, D; Gregersen, N; Koeberl, DD; Liu, HM; Matern, D; Millington, DS; Stevens, RD; Young, SP1
Gordon, N1
Belanger-Quintana, A; Bischoff, C; de la Mota, JL; Ferrer, I; García, MJ; Gregersen, N; Martin-Hernández, E; Martínez Pardo, M; Merinero, B; Pérez-Cerdá, C; Ruiz Sala, P; Ugarte, M; Vianey-Saban, C1
Duran, M; Hogeveen, M; Ijlst, L; Niezen-Koning, KE; van Maldegem, BT; Wanders, RJ; Waterham, HR; Wijburg, FA1
Duran, M; van Maldegem, BT; Wanders, RJ; Waterham, HR; Wijburg, FA1
Abdenur, JE; Barshop, BA; Cederbaum, SD; Chang, E; Deignan, JL; Dorrani, N; Feuchtbaum, L; Gallant, NM; Leydiker, K; Lorey, F; Neidich, J; Puckett, R; Tang, H; Wang, RY1

Trials

1 trial(s) available for butyrylcarnitine and ethylmalonic acid

ArticleYear
Flavin adenine dinucleotide status and the effects of high-dose riboflavin treatment in short-chain acyl-CoA dehydrogenase deficiency.
    Pediatric research, 2010, Volume: 67, Issue:3

    Topics: Adolescent; Biomarkers; Butyryl-CoA Dehydrogenase; Carnitine; Child; Child, Preschool; Female; Flavin-Adenine Dinucleotide; Genetic Predisposition to Disease; Humans; Infant; Lipid Metabolism, Inborn Errors; Male; Malonates; Mutation; Phenotype; Prospective Studies; Riboflavin; Treatment Outcome; Vitamin B Complex

2010

Other Studies

5 other study(ies) available for butyrylcarnitine and ethylmalonic acid

ArticleYear
A comparison of in vitro acylcarnitine profiling methods for the diagnosis of classical and variant short chain acyl-CoA dehydrogenase deficiency.
    Clinica chimica acta; international journal of clinical chemistry, 2003, Volume: 337, Issue:1-2

    Topics: Acyl-CoA Dehydrogenase; Butyric Acid; Butyryl-CoA Dehydrogenase; Carbon Isotopes; Carnitine; Deuterium; DNA Mutational Analysis; Fibroblasts; Heterozygote; Homozygote; Humans; Malonates; Mutation, Missense; Palmitic Acid; Palmitoylcarnitine; Polymorphism, Genetic; Sensitivity and Specificity; Spectrometry, Mass, Electrospray Ionization; Spiro Compounds

2003
Acyl-CoA dehydrogenase deficiency: varieties with neurological involvement.
    Developmental medicine and child neurology, 2005, Volume: 47, Issue:3

    Topics: Acyl-CoA Dehydrogenase; Carnitine; Child; Child, Preschool; Chromosome Aberrations; Developmental Disabilities; Diagnosis, Differential; Electron-Transferring Flavoproteins; Female; Genes, Recessive; Genetic Variation; Humans; Hypoglycemia; Infant; Infant, Newborn; Male; Malonates; Mass Spectrometry; Metabolism, Inborn Errors; Neonatal Screening; Nervous System Diseases; Pregnancy; Prenatal Diagnosis; Prognosis; Succinates; Sudden Infant Death

2005
Persistent increase of plasma butyryl/isobutyrylcarnitine concentrations as marker of SCAD defect and ethylmalonic encephalopathy.
    Journal of inherited metabolic disease, 2006, Volume: 29, Issue:5

    Topics: Brain Diseases; Butyryl-CoA Dehydrogenase; Carnitine; Humans; Malonates; Mitochondrial Proteins; Nervous System Diseases; Nucleocytoplasmic Transport Proteins

2006
Clinical, biochemical, and genetic heterogeneity in short-chain acyl-coenzyme A dehydrogenase deficiency.
    JAMA, 2006, Aug-23, Volume: 296, Issue:8

    Topics: Acyl-CoA Dehydrogenase; Adolescent; Carnitine; Child; Child, Preschool; Female; Genotype; Humans; Infant; Infant, Newborn; Male; Malonates; Metabolism, Inborn Errors; Mutation; Neonatal Screening; Netherlands; Phenotype; Retrospective Studies; Riboflavin; Vitamin B Complex

2006
Biochemical, molecular, and clinical characteristics of children with short chain acyl-CoA dehydrogenase deficiency detected by newborn screening in California.
    Molecular genetics and metabolism, 2012, Volume: 106, Issue:1

    Topics: Acyl Coenzyme A; Acyl-CoA Dehydrogenase; California; Carnitine; Female; Follow-Up Studies; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Male; Malonates; Neonatal Screening; Sequence Deletion; Succinates

2012