coenzyme a has been researched along with Muscular Diseases in 10 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (20.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (20.00) | 24.3611 |
| 2020's | 6 (60.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cunha, R; Fidalgo, C; Mendes, A; Rodrigues, F | 1 |
| Amar, SK; Edwards, CJ; Eren, E; Forster, T; Hajela, V; Hughes, R; Joseph, VMK; Kiely, PDW; Lloyd, M; Rose, EC; Smith, KA; Wheeler, RD | 1 |
| 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 |
| Aydingoz, U; Batu, ED; Haliloglu, G; Kasap Cuceoglu, M; Ozen, S; Sari, S; Sener, S; Talim, B; Yildiz, AE | 1 |
| Fukui, Y; Katsuyama, E; Morihara, R; Nakano, Y; Nishino, I; Sasaki, R; Takemoto, M; Yamashita, T; Yunoki, T | 1 |
| Ali, G; Chico, L; Ricci, G; Siciliano, G; Torri, F | 1 |
| Brininger, CM; Call, JA; Corona, BT; Flanagan, KE; Goldman, SM; Greising, SM | 1 |
| Charuvanij, S; Galindo-Feria, AS; Lundberg, IE; Nishino, I; Ohnuki, Y; Sangruchi, T; Sanmaneechai, O; Shiina, T; Suzuki, S; Tanboon, J | 1 |
| Penn, D; Schmidt-Sommerfeld, E | 1 |
| Vaisrub, S | 1 |
1 review(s) available for coenzyme a and Muscular Diseases
| Article | Year |
|---|---|
A Child with Refractory and Relapsing Anti-3-Hydroxy-3-Methylglutaryl-Coenzyme A Reductase Myopathy: Case-Based Review.
Topics: Adolescent; Autoantibodies; Child; Coenzyme A; Delayed Diagnosis; Female; Humans; Immunoglobulins, Intravenous; Male; Methotrexate; Muscle Weakness; Muscular Diseases; Oxidoreductases | 2023 |
9 other study(ies) available for coenzyme a and Muscular Diseases
| Article | Year |
|---|---|
Diagnosis of Statin-Induced Necrotizing Myopathy: Contribution of Anti-HMGCR Antibodies.
Topics: Autoantibodies; Autoimmune Diseases; Coenzyme A; Humans; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Muscular Diseases; Necrosis | 2022 |
Anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase antibodies: incidence using different testing criteria, and case series.
Topics: Adult; Autoantibodies; Autoimmune Diseases; Coenzyme A; Humans; Hydroxymethylglutaryl CoA Reductases; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Incidence; Muscle, Skeletal; Muscular Diseases; Myositis; Oxidoreductases | 2022 |
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 |
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 |
Anti-HMGCR antibodies and asymptomatic hyperCKemia. A case report.
Topics: Coenzyme A; Humans; Hydroxymethylglutaryl CoA Reductases; Male; Muscle, Skeletal; Muscular Diseases; Myositis; Necrosis; Oxidoreductases | 2021 |
Impact of volumetric muscle loss injury on persistent motoneuron axotomy.
Topics: Analysis of Variance; Animals; Axotomy; Cholera Toxin; Citrate (si)-Synthase; Coenzyme A; Disease Models, Animal; Functional Laterality; Male; Motor Neurons; Muscle Contraction; Muscle, Skeletal; Muscular Diseases; Organ Size; Rats; Rats, Inbred Lew; Spinal Cord; Time Factors | 2018 |
Concurrent positive anti-3-hydroxy-3-methylglutaryl-coenzyme a reductase antibody with reducing body myopathy: Possible double trouble.
Topics: Autoantibodies; Autoimmune Diseases; Child; Coenzyme A; Humans; Hydroxymethylglutaryl CoA Reductases; Male; Muscle, Skeletal; Muscular Diseases; Muscular Dystrophies; Myositis; Oxidoreductases | 2019 |
[Carnitine deficiency].
Topics: Carnitine; Carnitine Acyltransferases; Carnitine O-Palmitoyltransferase; Child; Coenzyme A; Cytochrome-c Oxidase Deficiency; Fatty Acid Desaturases; Fatty Acids; Humans; Ketones; Lipid Metabolism, Inborn Errors; Mitochondria, Liver; Mitochondria, Muscle; Muscular Diseases; Renal Aminoacidurias; Renal Dialysis; Transferases | 1986 |
Carnitine deficiency myopathy.
Topics: Adolescent; Carnitine; Coenzyme A; Female; Humans; Lipid Metabolism, Inborn Errors; Mitochondria, Muscle; Muscles; Muscular Diseases | 1973 |