s-adenosylmethionine has been researched along with Arrhythmia in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (25.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 1 (25.00) | 2.80 |
| Authors | Studies |
|---|---|
| Aldehaimi, A; Almannai, M; Almontashiri, NAM; Peake, RWA | 1 |
| Akaza, K; Bunai, Y; Ishii, A; Nagai, A; Nishida, N; Yamaguchi, S | 1 |
| Bollaert, PE; de Chillou, C; Feillet, F; Lefebvre, E; Sadoul, N; Steinmann, G; Vianey-Saban, C; Vidailhet, M | 1 |
| Bonnet, D; Brivet, M; Jouvet, P; Martin, D; Rabier, D; Saudubray, JM; Villain, E | 1 |
4 other study(ies) available for s-adenosylmethionine and Arrhythmia
| Article | Year |
|---|---|
Hyperammonemia, Lactic Acidosis, and Arrhythmia in a Newborn.
Topics: Acidosis, Lactic; Arrhythmias, Cardiac; Carnitine; Female; Humans; Hyperammonemia; Infant, Newborn; Lipid Metabolism, Inborn Errors; Membrane Transport Proteins; Mutation | 2021 |
A case of sudden death after Japanese encephalitis vaccination.
Topics: Anaphylaxis; Arrhythmias, Cardiac; Autopsy; C-Reactive Protein; Carnitine; Cause of Death; Child; Death, Sudden; Encephalitis, Japanese; Fatal Outcome; Heart Arrest; Humans; Japanese Encephalitis Vaccines; Male; Non-alcoholic Fatty Liver Disease; Psychotropic Drugs; Tandem Mass Spectrometry; Uncertainty | 2015 |
Adult presentation of MCAD deficiency revealed by coma and severe arrythmias.
Topics: Acyl-CoA Dehydrogenase; Adult; Arrhythmias, Cardiac; Carnitine; Coma; Critical Care; Dicarboxylic Acids; Humans; Male; Metabolism, Inborn Errors; Treatment Outcome | 2003 |
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 |