palmitoylcarnitine has been researched along with Muscle Disorders in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (66.67) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Letellier, T; Malgat, M; Mazat, JP | 1 |
| Chalmers, RA; English, N; Stanley, CA; Wigglesworth, JS | 1 |
| Bauer, MF; Gempel, K; Gerbitz, KD; Hofmann, S; Rettinger, A | 1 |
3 other study(ies) available for palmitoylcarnitine and Muscle Disorders
| Article | Year |
|---|---|
Control of oxidative phosphorylation in rat muscle mitochondria: implications for mitochondrial myopathies.
Topics: Animals; Electron Transport Complex III; Electron Transport Complex IV; Hindlimb; Malates; Mitochondria, Muscle; Muscular Diseases; NAD(P)H Dehydrogenase (Quinone); Oxidation-Reduction; Oxidative Phosphorylation; Oxygen Consumption; Palmitoylcarnitine; Pyruvates; Pyruvic Acid; Rats; Rotenone | 1993 |
Mitochondrial carnitine-acylcarnitine translocase deficiency presenting as sudden neonatal death.
Topics: Adult; Amnion; Breast Feeding; Carnitine; Carnitine Acyltransferases; Carnitine O-Palmitoyltransferase; Chorion; Diagnosis, Differential; Fasting; Fatal Outcome; Fatty Acid Desaturases; Fatty Acids; Fatty Liver; Female; Fetal Diseases; Fibroblasts; Genes, Recessive; Humans; Infant, Newborn; Kidney Diseases; Lipid Metabolism, Inborn Errors; Milk, Human; Mitochondria; Muscular Diseases; Oxidation-Reduction; Palmitoylcarnitine; Pregnancy; Prenatal Diagnosis; Skin; Stress, Physiological; Sudden Infant Death; Triglycerides | 1997 |
Tandem mass spectrometric assay for the determination of carnitine palmitoyltransferase II activity in muscle tissue.
Topics: Acetylcarnitine; Carnitine; Carnitine O-Acetyltransferase; Carnitine O-Palmitoyltransferase; Humans; Kinetics; Mass Spectrometry; Muscles; Muscular Diseases; Palmitoylcarnitine; Spectrophotometry | 2002 |