glycine has been researched along with Abnormal Movements 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 | 1 (33.33) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Fukao, T | 1 |
| Akiba, K | 1 |
| Goto, M | 1 |
| Kuwayama, N | 1 |
| Morita, M | 1 |
| Hori, T | 1 |
| Aoyama, Y | 1 |
| Venkatesan, R | 1 |
| Wierenga, R | 1 |
| Moriyama, Y | 1 |
| Hashimoto, T | 1 |
| Usuda, N | 1 |
| Murayama, K | 1 |
| Ohtake, A | 1 |
| Hasegawa, Y | 2 |
| Shigematsu, Y | 1 |
| Rizos, EN | 1 |
| Siafakas, N | 1 |
| Katsantoni, E | 1 |
| Lazou, V | 1 |
| Sakellaropoulos, K | 1 |
| Kastania, A | 1 |
| Kossida, S | 1 |
| Chatzigeorgiou, KS | 1 |
| Arsenis, G | 1 |
| Zerva, L | 1 |
| Katsafouros, K | 1 |
| Lykouras, L | 1 |
| Małek, LA | 1 |
| Labib, S | 1 |
| Mazurkiewicz, L | 1 |
| Saj, M | 1 |
| Płoski, R | 1 |
| Tesson, F | 1 |
| Bilińska, ZT | 1 |
3 other studies available for glycine 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; D | 2014 |
Association of the dopamine D3 receptor Ser9Gly and of the serotonin 2C receptor gene polymorphisms with tardive dyskinesia in Greeks with chronic schizophrenic disorder.
Topics: Amino Acid Substitution; Chronic Disease; Dyskinesias; Female; Genetic Predisposition to Disease; Gl | 2009 |
A new c.1621 C > G, p.R541G lamin A/C mutation in a family with DCM and regional wall motion abnormalities (akinesis/dyskinesis): genotype-phenotype correlation.
Topics: Amino Acid Substitution; Arginine; Cardiomyopathy, Dilated; Dyskinesias; Family; Genetic Association | 2011 |