s-adenosylmethionine has been researched along with Mitochondrial Myopathies in 10 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (20.00) | 18.2507 |
| 2000's | 4 (40.00) | 29.6817 |
| 2010's | 3 (30.00) | 24.3611 |
| 2020's | 1 (10.00) | 2.80 |
| Authors | Studies |
|---|---|
| Adam, T; Chrastina, P; Farolfi, M; Foltenová, H; Friedecký, D; Hanák, P; Honzík, T; Hrubá, E; Ješina, P; Kousal, B; Kožich, V; Pavlíková, M; Rücklová, K; Smolka, V; Vlášková, H; Zeman, J | 1 |
| Christensen, M; Dunø, M; Vissing, CR; Vissing, J; Wibrand, F | 1 |
| Ask, S; Gustafsson, J; Haglind, CB; Nordenström, A; Stenlid, MH; von Döbeln, U | 1 |
| Hiramatsu, Y; Izumi, Y; Kaji, R; Matsui, N; Miyazaki, Y; Nodera, H; Takashima, H; Yamamoto, Y | 1 |
| Jumma, O; Ogundare, O; Turnbull, DM; Woywodt, A | 1 |
| Chang, YS; Jin, DK; Ki, CS; Kim, SR; Lee, SY; Park, HD; Park, WS | 1 |
| Armstrong, DL; Scaglia, F; Scheuerle, AE; Sweetman, L; Towbin, JA; Wong, LJ | 1 |
| Andersen, O; Andresen, BS; Beresford, MW; Cornelius, N; Dean, JC; Frerman, FE; Gregersen, N; Holme, E; Merinero, B; Miedzybrodzka, ZH; Morris, AA; Oldfors, A; Olpin, SE; Olsen, RK; Pourfarzam, M; Turnbull, DM | 1 |
| Becker, LE; Bennett, MJ; Haslam, RH; Rhead, WJ; Tein, I; Vockley, J | 1 |
| Bonnet, D; Brivet, M; Jouvet, P; Martin, D; Rabier, D; Saudubray, JM; Villain, E | 1 |
10 other study(ies) available for s-adenosylmethionine and Mitochondrial Myopathies
| Article | Year |
|---|---|
Impact of Newborn Screening and Early Dietary Management on Clinical Outcome of Patients with Long Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency and Medium Chain Acyl-CoA Dehydrogenase Deficiency-A Retrospective Nationwide Study.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Acyl-CoA Dehydrogenase; Cardiomyopathies; Carnitine; Child; Child, Preschool; Czech Republic; Female; Humans; Incidence; Infant; Infant, Newborn; Lipid Metabolism, Inborn Errors; Male; Metabolism, Inborn Errors; Mitochondrial Myopathies; Mitochondrial Trifunctional Protein; Neonatal Screening; Nervous System Diseases; Outcome Assessment, Health Care; Retrospective Studies; Rhabdomyolysis; Severity of Illness Index | 2021 |
Hydroxylated Long-Chain Acylcarnitines are Biomarkers of Mitochondrial Myopathy.
Topics: Acyl Coenzyme A; Acyl-CoA Dehydrogenase; Adult; Biomarkers; Carnitine; Cohort Studies; Denmark; Female; Humans; Hydroxylation; Male; Middle Aged; Mitochondrial Myopathies; Mixed Function Oxygenases; Oxidation-Reduction; Prospective Studies | 2019 |
Increased and early lipolysis in children with long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency during fast.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Age Factors; Biomarkers; Blood Glucose; Calorimetry, Indirect; Cardiomyopathies; Carnitine; Child; Child, Preschool; Energy Metabolism; Fasting; Female; Glycerol; Humans; Hyperglycemia; Isotope Labeling; Lipid Metabolism, Inborn Errors; Lipolysis; Male; Microdialysis; Mitochondrial Myopathies; Mitochondrial Trifunctional Protein; Nervous System Diseases; Postprandial Period; Rhabdomyolysis; Time Factors | 2015 |
Mitochondrial trifunctional protein deficiency: an adult patient with similar progress to Charcot-Marie-Tooth disease.
Topics: Biomarkers; Cardiomyopathies; Carnitine; Charcot-Marie-Tooth Disease; Diagnosis, Differential; Disease Progression; Genetic Testing; Humans; Lipid Metabolism, Inborn Errors; Male; Middle Aged; Mitochondrial Myopathies; Mitochondrial Trifunctional Protein; Mitochondrial Trifunctional Protein, beta Subunit; Mutation; Nervous System Diseases; Peripheral Nervous System Diseases; Recurrence; Rhabdomyolysis | 2017 |
Searching for the needle in the Haystacks.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Age of Onset; Biopsy; Carnitine; Creatine Kinase; Creatinine; Histocytochemistry; Humans; Male; Middle Aged; Mitochondrial Myopathies; Prognosis; Rare Diseases; Recurrence; Rhabdomyolysis; Walking | 2009 |
Two novel HADHB gene mutations in a Korean patient with mitochondrial trifunctional protein deficiency.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Cardiomyopathies; Carnitine; DNA Mutational Analysis; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Male; Mitochondria; Mitochondrial Myopathies; Mitochondrial Proteins; Mitochondrial Trifunctional Protein; Mitochondrial Trifunctional Protein, beta Subunit; Multienzyme Complexes; Mutation; Nervous System Diseases; Peripheral Nervous System Diseases; Republic of Korea; Retinitis Pigmentosa; Rhabdomyolysis | 2009 |
Neonatal presentation of ventricular tachycardia and a Reye-like syndrome episode associated with disturbed mitochondrial energy metabolism.
Topics: Biomarkers; Carnitine; DNA, Mitochondrial; Female; Glutarates; Humans; Infant, Newborn; Mitochondrial Myopathies; Mutation; Orotic Acid; Reye Syndrome; Tachycardia, Ventricular | 2002 |
ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency.
Topics: Acyl-CoA Dehydrogenase; Adolescent; Adult; Brain Diseases, Metabolic; Carnitine; Child; Child, Preschool; Electron Transport; Electron-Transferring Flavoproteins; Fatty Acids; Female; Humans; Iron-Sulfur Proteins; Male; Metabolism, Inborn Errors; Mitochondria, Muscle; Mitochondrial Myopathies; Muscle, Skeletal; Mutation; Oxidation-Reduction; Oxidoreductases Acting on CH-NH Group Donors; Riboflavin | 2007 |
Short-chain acyl-CoA dehydrogenase deficiency: a cause of ophthalmoplegia and multicore myopathy.
Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Adolescent; Carnitine; Cells, Cultured; Diagnosis, Differential; Female; Fibroblasts; Humans; Mitochondrial Myopathies; Ophthalmoplegia, Chronic Progressive External; Phenotype | 1999 |
Arrhythmias and conduction defects as presenting symptoms of fatty acid oxidation disorders in children.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenase, Long-Chain; Arrhythmias, Cardiac; Carnitine; Carnitine Acyltransferases; Carnitine O-Palmitoyltransferase; Fatty Acid Desaturases; Fatty Acids; Female; Heart Conduction System; Humans; Infant; Infant, Newborn; Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase; Male; Mitochondria, Heart; Mitochondrial Myopathies; Models, Biological; Oxidation-Reduction; Sudden Infant Death; Tachycardia, Ventricular | 1999 |