coenzyme a has been researched along with Muscular Dystrophy in 6 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 5 (83.33) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (16.67) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Charuvanij, S; Galindo-Feria, AS; Lundberg, IE; Nishino, I; Ohnuki, Y; Sangruchi, T; Sanmaneechai, O; Shiina, T; Suzuki, S; Tanboon, J | 1 |
Brooke, MH; Carroll, JE; Norris, BJ; Trefz, JI; Villadiego, A | 1 |
Radu, H | 1 |
Kapusi, A; Radu, H; Stenzel, K | 1 |
Keresztes, L; Radu, H; Stenzel, K | 1 |
Radu, H; Stenzel, K | 1 |
6 other study(ies) available for coenzyme a and Muscular Dystrophy
Article | Year |
---|---|
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 |
'Dystrophic' lipid myopathy in two sisters.
Topics: Child; Child, Preschool; Coenzyme A; Female; Humans; Lipid Metabolism; Muscular Dystrophies; Oxidation-Reduction; Palmitates; Pyruvates | 1986 |
Coenzymatic therapy in progressive muscular dystrophy.
Topics: Child; Coenzyme A; Cytochromes; Diseases in Twins; Female; Humans; Male; Muscular Dystrophies; NAD; Phosphocreatine | 1973 |
Defect of coenzyme-A activity in progessive muscular dystrophy.
Topics: Aspartic Acid; Child; Child, Preschool; Citric Acid Cycle; Coenzyme A; Extracellular Space; Glutamates; Glycolysis; Humans; Ketoglutaric Acids; Male; Metabolic Diseases; Muscles; Muscular Dystrophies; Oxaloacetates | 1968 |
[Effects of administration of phosphocreatine on the clinical, biochemical and electromyographic evolution of Duchenne's progressive muscular dystrophy].
Topics: Child; Child, Preschool; Coenzyme A; Creatine; Creatine Kinase; Creatinine; Electromyography; Fructose-Bisphosphate Aldolase; Humans; L-Lactate Dehydrogenase; Muscular Dystrophies; Phosphocreatine; Transaminases | 1968 |
[Contribution on the study of pseudohypertrophic muscular dystrophies. I. Benign pseudohypertrophic muscular dystrophy].
Topics: Adolescent; Adult; Alanine Transaminase; Aspartate Aminotransferases; Biopsy; Coenzyme A; Creatine Kinase; Diagnosis, Differential; Electromyography; Fructose-Bisphosphate Aldolase; Humans; L-Lactate Dehydrogenase; Male; Muscles; Muscular Dystrophies; Pedigree; Phenotype | 1969 |