s-adenosylmethionine has been researched along with Abnormal Movements in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Akiba, K; Aoyama, Y; Fukao, T; Goto, M; Hasegawa, Y; Hashimoto, T; Hori, T; Kuwayama, N; Morita, M; Moriyama, Y; Murayama, K; Ohtake, A; Shigematsu, Y; Usuda, N; Venkatesan, R; Wierenga, R | 1 |
| Priebe, S; Turner, T; Werneke, U | 1 |
1 review(s) available for s-adenosylmethionine and Abnormal Movements
| Article | Year |
|---|---|
Complementary medicines in psychiatry: review of effectiveness and safety.
Topics: Antidepressive Agents; Antipsychotic Agents; Cognition Disorders; Complementary Therapies; Dementia; Dyskinesias; Ergoloid Mesylates; Folic Acid; Humans; Hypnotics and Sedatives; Mental Disorders; Nootropic Agents; Phytotherapy; Plant Preparations; S-Adenosylmethionine; Selenium; Substance-Related Disorders | 2006 |
1 other study(ies) available for s-adenosylmethionine and Abnormal Movements
| Article | Year |
|---|---|
The first case in Asia of 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency (HSD10 disease) with atypical presentation.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Acetyl-CoA C-Acetyltransferase; Base Sequence; Carnitine; Child; Diagnosis, Differential; DNA Mutational Analysis; Dyskinesias; Fibroblasts; Glycine; Humans; Hydroxybutyrates; Immunoblotting; Lipid Metabolism, Inborn Errors; Male; Mental Retardation, X-Linked; Mitochondria; Models, Molecular; Point Mutation; Protein Structure, Tertiary | 2014 |