isoleucine has been researched along with Lipid Metabolism, Inborn Error in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Akiyama, M; Nakajima, K; Sano, S; Shimizu, H; Teraishi, M; Uchida, Y; Ujihara, M; Yamamoto, M | 1 |
| Brand, J; Hoffmann, GF; Lindner, M; Mayatepek, E; Ruiter, JP; Wanders, RJ; Zschocke, J | 1 |
2 other study(ies) available for isoleucine and Lipid Metabolism, Inborn Error
| Article | Year |
|---|---|
Epidermal triglyceride levels are correlated with severity of ichthyosis in Dorfman-Chanarin syndrome.
Topics: 1-Acylglycerol-3-Phosphate O-Acyltransferase; Amino Acid Substitution; Asian People; Base Sequence; Epidermis; Exons; Genes, Recessive; Heterozygote; Humans; Ichthyosis, Lamellar; Isoleucine; Lipid Metabolism, Inborn Errors; Lipids; Male; Microscopy, Electron; Middle Aged; Mutation, Missense; Point Mutation; Seasons; Severity of Illness Index; Skin; Threonine; Triglycerides | 2010 |
Progressive infantile neurodegeneration caused by 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency: a novel inborn error of branched-chain fatty acid and isoleucine metabolism.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Acetyl-CoA C-Acyltransferase; Alcohol Oxidoreductases; Amino Acid Metabolism, Inborn Errors; Diagnosis, Differential; Disease Progression; Fatty Acids; Hemophilia A; Humans; Infant, Newborn; Intellectual Disability; Isoleucine; Lipid Metabolism, Inborn Errors; Male; Mitochondria; Neurodegenerative Diseases; Oxidation-Reduction; Psychomotor Agitation; Seizures | 2000 |