Page last updated: 2024-08-21

ethylmalonic acid and palmitic acid

ethylmalonic acid has been researched along with palmitic acid in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Boutron, A; Brivet, M; Haengeli, CA; Khellaf, A; Lemonnier, A; Rocchiccioli, F; Tardieu, M	1
Bali, D; Gregersen, N; Koeberl, DD; Liu, HM; Matern, D; Millington, DS; Stevens, RD; Young, SP	1

Other Studies

2 other study(ies) available for ethylmalonic acid and palmitic acid

Article	Year
Riboflavin responsive ethylmalonic-adipic aciduria in a 9-month-old boy with liver cirrhosis, myopathy and encephalopathy. Journal of inherited metabolic disease, 1991, Volume: 14, Issue:3 Topics: 3-Hydroxyacyl CoA Dehydrogenases; Adipates; Brain Diseases; Fatty Acids; Female; Fibroblasts; Humans; Infant; Liver Cirrhosis; Malonates; Metabolism, Inborn Errors; Muscular Diseases; Myristic Acid; Myristic Acids; Oxidation-Reduction; Palmitic Acid; Palmitic Acids; Riboflavin	1991
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

Article

Year

Riboflavin responsive ethylmalonic-adipic aciduria in a 9-month-old boy with liver cirrhosis, myopathy and encephalopathy.

Journal of inherited metabolic disease, 1991, Volume: 14, Issue:3

Topics: 3-Hydroxyacyl CoA Dehydrogenases; Adipates; Brain Diseases; Fatty Acids; Female; Fibroblasts; Humans; Infant; Liver Cirrhosis; Malonates; Metabolism, Inborn Errors; Muscular Diseases; Myristic Acid; Myristic Acids; Oxidation-Reduction; Palmitic Acid; Palmitic Acids; Riboflavin

1991

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