carnitine has been researched along with Autosomal Chromosome Disorders in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (50.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Gellera, C | 1 |
| Uziel, G | 1 |
| Rimoldi, M | 1 |
| Zeviani, M | 1 |
| Laverda, A | 1 |
| Carrara, F | 1 |
| DiDonato, S | 1 |
| Shahar, E | 1 |
| Brand, N | 1 |
| Shapira, Y | 1 |
| Barash, V | 1 |
| Gutman, A | 1 |
2 other studies available for carnitine and Autosomal Chromosome Disorders
| Article | Year |
|---|---|
Fumarase deficiency is an autosomal recessive encephalopathy affecting both the mitochondrial and the cytosolic enzymes.
Topics: Acids; Blotting, Western; Brain Diseases, Metabolic; Carnitine; Chromatography, Gas; Chromosome Aber | 1990 |
Familial carnitine deficiency: further evidence for autosomal recessive transmission with variable expression.
Topics: Carnitine; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Female; Gene Expression R | 1988 |