carnitine has been researched along with Mucopolysaccharidosis III in 1 studies
Mucopolysaccharidosis III: Mucopolysaccharidosis characterized by heparitin sulfate in the urine, progressive mental retardation, mild dwarfism, and other skeletal disorders. There are four clinically indistinguishable but biochemically distinct forms, each due to a deficiency of a different enzyme.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (100.00) | 2.80 |
| Authors | Studies |
|---|---|
| De Pasquale, V | 1 |
| Caterino, M | 1 |
| Costanzo, M | 1 |
| Fedele, R | 1 |
| Ruoppolo, M | 1 |
| Pavone, LM | 1 |
1 other study available for carnitine and Mucopolysaccharidosis III
| Article | Year |
|---|---|
Targeted Metabolomic Analysis of a Mucopolysaccharidosis IIIB Mouse Model Reveals an Imbalance of Branched-Chain Amino Acid and Fatty Acid Metabolism.
Topics: Amino Acids, Aromatic; Amino Acids, Branched-Chain; Animals; Carnitine; Disease Models, Animal; Huma | 2020 |