s-adenosylmethionine has been researched along with Atrophy in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (60.00) | 29.6817 |
| 2010's | 1 (20.00) | 24.3611 |
| 2020's | 1 (20.00) | 2.80 |
| Authors | Studies |
|---|---|
| Davatzikos, C; Erus, G; Ferrucci, L; Mitchell, BA; Moaddel, R; Resnick, SM; Tian, Q | 1 |
| Bain, MD; Baric, I; Chalmers, RA; Feyh, P; Hoffmann, GF; Jakobs, C; Jeffrey, I; Kölker, S; Okun, JG; Pourfarzam, M; Schor, DS; Wagner, L; Zschocke, J | 1 |
| Anderson, BD; Freedenberg, D; Hahn, SH; Kramer, KA; Oglesbee, D | 1 |
| Flitton, M; Knight, HM; Macdonald, IA; Rielly, N; Smith, AD; Warden, D; Warman, R | 1 |
| Chazerain, P; Moulonguet, A; Olivero de Rubiana, JP; Vinciguerra, C; Ziza, JM | 1 |
1 review(s) available for s-adenosylmethionine and Atrophy
| Article | Year |
|---|---|
[Postoperative combined medullary sclerosis revealing Biermer's disease: toxic effect of nitrous oxide].
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Abscess; Aged; Anemia, Pernicious; Anesthetics, Inhalation; Arthroplasty, Replacement, Hip; Atrophy; Autoantibodies; Autoimmune Diseases; Demyelinating Diseases; Female; Gastric Mucosa; Humans; Intestinal Absorption; Intrinsic Factor; Nitrous Oxide; Oxidation-Reduction; Paresthesia; Postoperative Complications; Proprioception; S-Adenosylmethionine; Sclerosis; Spinal Cord; Spinal Cord Diseases; Surgical Wound Infection; Vitamin B 12 | 2000 |
4 other study(ies) available for s-adenosylmethionine and Atrophy
| Article | Year |
|---|---|
Sex differences in plasma lipid profiles of accelerated brain aging.
Topics: Aging; Atrophy; Brain; Ceramides; Female; Humans; Male; Sex Characteristics; Triglycerides | 2023 |
Glutaryl-CoA dehydrogenase deficiency: region-specific analysis of organic acids and acylcarnitines in post mortem brain predicts vulnerability of the putamen.
Topics: Acidosis; Acute Disease; Adolescent; Anticonvulsants; Atrophy; Brain; Carnitine; DNA Mutational Analysis; Fatal Outcome; Gas Chromatography-Mass Spectrometry; Gene Expression; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Male; Muscle Hypotonia; N-Methylaspartate; Oxidoreductases Acting on CH-CH Group Donors; Point Mutation; Putamen; Spasm; Vigabatrin | 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 |
Interaction of nutrition and genetics via DNMT3L-mediated DNA methylation determines cognitive decline.
Topics: Aged; Aged, 80 and over; Atrophy; Brain; Cognition; Cognitive Dysfunction; DNA (Cytosine-5-)-Methyltransferases; DNA Methylation; Female; Homocysteine; Humans; Male; S-Adenosylmethionine; Spatial Memory; Vitamin B Complex | 2019 |