carnitine has been researched along with Auditory Processing Disorder, Central in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Waisbren, SE | 1 |
| Landau, Y | 1 |
| Wilson, J | 1 |
| Vockley, J | 1 |
| Eminoglu, FT | 1 |
| Ozcelik, AA | 1 |
| Okur, I | 1 |
| Tumer, L | 1 |
| Biberoglu, G | 1 |
| Demir, E | 1 |
| Hasanoglu, A | 1 |
| Baumgartner, MR | 1 |
| Ly, TB | 1 |
| Peters, V | 1 |
| Gibson, KM | 1 |
| Liesert, M | 1 |
| Buckel, W | 1 |
| Wilcken, B | 1 |
| Carpenter, K | 1 |
| Ensenauer, R | 1 |
| Hoffmann, GF | 1 |
| Mack, M | 1 |
| Zschocke, J | 1 |
3 other studies available for carnitine and Auditory Processing Disorder, Central
| Article | Year |
|---|---|
Neuropsychological outcomes in fatty acid oxidation disorders: 85 cases detected by newborn screening.
Topics: Acyl-CoA Dehydrogenase; Carnitine; Child; Child, Preschool; Developmental Disabilities; Fatty Acids; | 2013 |
3-Methylcrotonyl-CoA carboxylase deficiency: phenotypic variability in a family.
Topics: Adult; Brain; Carbon-Carbon Ligases; Carnitine; Cells, Cultured; Child, Preschool; DNA Mutational An | 2009 |
Mutations in the AUH gene cause 3-methylglutaconic aciduria type I.
Topics: Amino Acid Metabolism, Inborn Errors; Carnitine; Child, Preschool; Exons; Genes, Recessive; Glutarat | 2003 |