s-adenosylmethionine has been researched along with Acidosis, Lactic in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Aldehaimi, A; Almannai, M; Almontashiri, NAM; Peake, RWA | 1 |
| Bocian, M; Boyle, K; Gargus, JJ; Roe, CR; Roe, DS; Vianey-Saban, C | 1 |
| Anderson, BD; Freedenberg, D; Hahn, SH; Kramer, KA; Oglesbee, D | 1 |
3 other study(ies) available for s-adenosylmethionine and Acidosis, Lactic
| 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 |
Respiratory complex II defect in siblings associated with a symptomatic secondary block in fatty acid oxidation.
Topics: Acidosis, Lactic; Acyl-CoA Dehydrogenase; Behavior; Bicarbonates; Carnitine; Cell Line; Fatty Acids; Female; Fibroblasts; Growth; Humans; Infant, Newborn; Lactic Acid; Mitochondrial Diseases; Oxidation-Reduction; Oxidative Phosphorylation; Phenotype | 2003 |
Normal muscle respiratory chain enzymes can complicate mitochondrial disease diagnosis.
Topics: Acidosis, Lactic; Atrophy; Biopsy; Blotting, Western; Carnitine; Central Nervous System Cysts; Cerebral Ventricles; Diagnosis, Differential; DNA Mutational Analysis; Electron Transport Complex I; Female; Fibroblasts; Frontal Lobe; Humans; Infant, Newborn; Magnetic Resonance Imaging; Mitochondrial Diseases; Muscle, Skeletal; Nerve Fibers, Myelinated; Point Mutation | 2006 |