palmitic acid has been researched along with Inborn Errors of Metabolism in 6 studies
Palmitic Acid: A common saturated fatty acid found in fats and waxes including olive oil, palm oil, and body lipids.
hexadecanoic acid : A straight-chain, sixteen-carbon, saturated long-chain fatty acid.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 3 (50.00) | 18.2507 |
| 2000's | 1 (16.67) | 29.6817 |
| 2010's | 2 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Fontaine, M | 1 |
| Kim, I | 1 |
| Dessein, AF | 1 |
| Mention-Mulliez, K | 1 |
| Dobbelaere, D | 1 |
| Douillard, C | 1 |
| Sole, G | 1 |
| Schiff, M | 1 |
| Jaussaud, R | 1 |
| Espil-Taris, C | 1 |
| Boutron, A | 2 |
| Wuyts, W | 1 |
| Acquaviva, C | 1 |
| Vianey-Saban, C | 1 |
| Roland, D | 1 |
| Joncquel-Chevalier Curt, M | 1 |
| Vamecq, J | 1 |
| Gélinas, R | 1 |
| Thompson-Legault, J | 1 |
| Bouchard, B | 1 |
| Daneault, C | 1 |
| Mansour, A | 1 |
| Gillis, MA | 1 |
| Charron, G | 1 |
| Gavino, V | 1 |
| Labarthe, F | 1 |
| Des Rosiers, C | 1 |
| Schulze-Bergkamen, A | 1 |
| Okun, JG | 1 |
| Spiekerkötter, U | 1 |
| Lindner, M | 1 |
| Haas, D | 1 |
| Kohlmüller, D | 1 |
| Mayatepek, E | 1 |
| Schulze-Bergkamen, H | 1 |
| Greenberg, CR | 1 |
| Zschocke, J | 1 |
| Hoffmann, GF | 1 |
| Kölker, S | 1 |
| Kelly, DP | 1 |
| Mendelsohn, NJ | 1 |
| Sobel, BE | 1 |
| Bergmann, SR | 1 |
| Roe, CR | 1 |
| Roe, DS | 1 |
| Brivet, M | 1 |
| Tardieu, M | 1 |
| Khellaf, A | 1 |
| Rocchiccioli, F | 1 |
| Haengeli, CA | 1 |
| Lemonnier, A | 1 |
1 review available for palmitic acid and Inborn Errors of Metabolism
| Article | Year |
|---|---|
Recent developments in the investigation of inherited metabolic disorders using cultured human cells.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Carnitine; Carnitine O-Palmitoyltransferase; Cell Line; Fatty Acid | 1999 |
5 other studies available for palmitic acid and Inborn Errors of Metabolism
| Article | Year |
|---|---|
Fluxomic assay-assisted diagnosis orientation in a cohort of 11 patients with myopathic form of CPT2 deficiency.
Topics: Adolescent; Adult; Biomarkers; Carnitine O-Palmitoyltransferase; Child; Child, Preschool; Female; Fo | 2018 |
Prolonged QT interval and lipid alterations beyond β-oxidation in very long-chain acyl-CoA dehydrogenase null mouse hearts.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Age Factors; Aging; Analysis of Variance; Animals; Congenital Bo | 2011 |
Quantitative acylcarnitine profiling in peripheral blood mononuclear cells using in vitro loading with palmitic and 2-oxoadipic acids: biochemical confirmation of fatty acid oxidation and organic acid disorders.
Topics: Adipates; Carnitine; Child; Child, Preschool; Female; Humans; Infant; Male; Mass Spectrometry; Metab | 2005 |
Detection and assessment by positron emission tomography of a genetically determined defect in myocardial fatty acid utilization (long-chain acyl-CoA dehydrogenase deficiency).
Topics: Acetates; Acyl-CoA Dehydrogenase, Long-Chain; Adult; Carbon Dioxide; Carbon Radioisotopes; Child; Ch | 1993 |
Riboflavin responsive ethylmalonic-adipic aciduria in a 9-month-old boy with liver cirrhosis, myopathy and encephalopathy.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Adipates; Brain Diseases; Fatty Acids; Female; Fibroblasts; Humans | 1991 |