acetylcarnitine has been researched along with Cystic Fibrosis in 1 studies
Acetylcarnitine: An acetic acid ester of CARNITINE that facilitates movement of ACETYL COA into the matrices of mammalian MITOCHONDRIA during the oxidation of FATTY ACIDS.
Cystic Fibrosis: An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Acylcarnitine is low in cord blood in patients with cystic fibrosis, suggesting that fatty acid metabolism is disturbed in utero." | 7.68 | Carnitine metabolites in infants with cystic fibrosis: a prospective study. ( Lloyd-Still, JD; Powers, CA; Wessel, HU, 1993) |
| "Acylcarnitine is low in cord blood in patients with cystic fibrosis, suggesting that fatty acid metabolism is disturbed in utero." | 3.68 | Carnitine metabolites in infants with cystic fibrosis: a prospective study. ( Lloyd-Still, JD; Powers, CA; Wessel, HU, 1993) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (100.00) | 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 |
|---|---|
| Lloyd-Still, JD | 1 |
| Powers, CA | 1 |
| Wessel, HU | 1 |
1 other study available for acetylcarnitine and Cystic Fibrosis
| Article | Year |
|---|---|
Carnitine metabolites in infants with cystic fibrosis: a prospective study.
Topics: Acetylcarnitine; Age Factors; Carnitine; Child, Preschool; Cystic Fibrosis; Energy Metabolism; Human | 1993 |