coenzyme a has been researched along with Rhabdomyolysis in 4 studies
| 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 | 4 (100.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cole, D; Darin, N; Donker Kaat, L; Doolaard, M; Ebberink, MS; Ferdinandusse, S; Fuchs, SA; Hedberg-Oldfors, C; Huidekoper, HH; Moat, SJ; Olpin, S; Régal, L; Ruiter, JPN; Schwantje, M; Visser, G | 1 |
| Astrowski, AA; Kanunnikova, NP; Lukiyenko, EP; Plotnikov, EY; Semenovich, DS | 1 |
| Fukui, Y; Katsuyama, E; Morihara, R; Nakano, Y; Nishino, I; Sasaki, R; Takemoto, M; Yamashita, T; Yunoki, T | 1 |
| Gokmen-Ozel, H; Kadayifcilar, S; Kahraman, AB; Sivri, S; Yildiz, Y | 1 |
4 other study(ies) available for coenzyme a and Rhabdomyolysis
| Article | Year |
|---|---|
Thermo-sensitive mitochondrial trifunctional protein deficiency presenting with episodic myopathy.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Adolescent; Cardiomyopathies; Child; Child, Preschool; Coenzyme A; Delayed Diagnosis; Fatty Acids; Humans; Lipid Metabolism, Inborn Errors; Mitochondrial Myopathies; Mitochondrial Trifunctional Protein; Muscular Diseases; Nervous System Diseases; Rhabdomyolysis | 2022 |
Protective Effect of D-Panthenol in Rhabdomyolysis-Induced Acute Kidney Injury.
Topics: Acute Kidney Injury; Animals; Antioxidants; Catalase; Coenzyme A; Creatine Kinase; Creatinine; Glutathione; Glutathione Peroxidase; Glycerol; Kidney; Lactate Dehydrogenases; Male; Oxidative Stress; Rats; Rats, Wistar; Rhabdomyolysis; Superoxide Dismutase | 2022 |
A young female case of asymptomatic immune-mediated necrotizing myopathy: a potential diagnostic option of antibody testing for rhabdomyolysis.
Topics: Adolescent; Autoantibodies; Autoimmune Diseases; Coenzyme A; Female; Humans; Muscle, Skeletal; Muscular Diseases; Myositis; Necrosis; Oxidoreductases; Rhabdomyolysis | 2023 |
Successful management of rhabdomyolysis with triheptanoin in a child with severe long-chain 3-hydroxyacyl-coenzyme A dehydrogenase (LCHAD) deficiency.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Child; Coenzyme A; Female; Humans; Infant; Lipid Metabolism, Inborn Errors; Oxidation-Reduction; Rhabdomyolysis; Triglycerides | 2023 |