lactic acid has been researched along with Dyskinesia Syndromes in 6 studies
Lactic Acid: A normal intermediate in the fermentation (oxidation, metabolism) of sugar. The concentrated form is used internally to prevent gastrointestinal fermentation. (From Stedman, 26th ed)
2-hydroxypropanoic acid : A 2-hydroxy monocarboxylic acid that is propanoic acid in which one of the alpha-hydrogens is replaced by a hydroxy group.
| Excerpt | Relevance | Reference |
|---|---|---|
| "D-Allose was intravenously injected before and after ischemia (200 mg/kg)." | 1.40 | The effects of D-allose on transient ischemic neuronal death and analysis of its mechanism. ( Itano, T; Keep, RF; Liu, Y; Nakamura, T; Shinomiya, A; Tamiya, T; Tokuda, M; Toyoshima, T, 2014) |
| "Both patients had PDH deficiency caused by a new mutation (G585C) in the PDHA1 gene, which is predicted to replace a highly conserved glycine at codon 195 by alanine." | 1.35 | Pyruvate dehydrogenase deficiency presenting as intermittent isolated acute ataxia. ( Debray, FG; Gagne, R; Laframboise, R; Lambert, M; MacKay, N; Maranda, B; Mitchell, GA; Robinson, BH, 2008) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (33.33) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (33.33) | 29.6817 |
| 2010's | 2 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Liu, Y | 1 |
| Nakamura, T | 1 |
| Toyoshima, T | 1 |
| Shinomiya, A | 1 |
| Tamiya, T | 1 |
| Tokuda, M | 1 |
| Keep, RF | 1 |
| Itano, T | 1 |
| Aguiar, AS | 1 |
| Tuon, T | 1 |
| Albuquerque, MM | 1 |
| Rocha, GS | 1 |
| Speck, AE | 1 |
| Araújo, JC | 1 |
| Dafré, AL | 1 |
| Prediger, RD | 1 |
| Pinho, RA | 1 |
| Glavina, T | 1 |
| Mrass, D | 1 |
| Dodig, T | 1 |
| Glavina, G | 1 |
| Pranić, S | 1 |
| Uglešić, B | 1 |
| Debray, FG | 1 |
| Lambert, M | 1 |
| Gagne, R | 1 |
| Maranda, B | 1 |
| Laframboise, R | 1 |
| MacKay, N | 1 |
| Robinson, BH | 1 |
| Mitchell, GA | 1 |
| Stansbie, D | 1 |
| Wallace, SJ | 1 |
| Marsac, C | 1 |
| Haas, RH | 1 |
| Rice, MA | 1 |
| Trauner, DA | 1 |
| Merritt, TA | 1 |
| Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
|---|---|---|---|---|---|---|---|
| Blood Lactate Levels in Patients Treated With Typical or Atypical Antipsychotics[NCT01139463] | 60 participants (Actual) | Observational | 2008-06-30 | Completed | |||
| [information is prepared from clinicaltrials.gov, extracted Sep-2024] | |||||||
1 review available for lactic acid and Dyskinesia Syndromes
| Article | Year |
|---|---|
Disorders of the pyruvate dehydrogenase complex.
Topics: Acetyl Coenzyme A; Acetyltransferases; Acidosis; Brain; Carbon Dioxide; Child; Child, Preschool; Coe | 1986 |
1 trial available for lactic acid and Dyskinesia Syndromes
| Article | Year |
|---|---|
Blood lactate levels in patients receiving first- or second- generation antipsychotics.
Topics: Adult; Antipsychotic Agents; Benzodiazepines; Dopamine Antagonists; Drug Monitoring; Haloperidol; Hu | 2011 |
4 other studies available for lactic acid and Dyskinesia Syndromes
| Article | Year |
|---|---|
The effects of D-allose on transient ischemic neuronal death and analysis of its mechanism.
Topics: 8-Hydroxy-2'-Deoxyguanosine; Analysis of Variance; Animals; Cerebral Cortex; Deoxyguanosine; Disease | 2014 |
The exercise redox paradigm in the Down's syndrome: improvements in motor function and increases in blood oxidative status in young adults.
Topics: Adult; Antioxidants; Biomarkers; Brain; Brain Diseases, Metabolic, Inborn; Catalase; Down Syndrome; | 2008 |
Pyruvate dehydrogenase deficiency presenting as intermittent isolated acute ataxia.
Topics: Ataxia; Basal Ganglia Diseases; Binding Sites; Brain Diseases, Metabolic; Child; Child, Preschool; D | 2008 |
Therapeutic effects of a ketogenic diet in Rett syndrome.
Topics: Ammonia; Blood Glucose; Child; Child, Preschool; Dietary Fats; Electroencephalography; Energy Intake | 1986 |