tyrosine has been researched along with Action Myoclonus-Renal Failure Syndrome 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 |
|---|---|
| Farhan, SM; Hegele, RA; Murphy, LM; Prasad, AN; Robinson, JF; Rupar, CA; Siu, VM; Wang, J | 1 |
| Kawano, H; Matsushita, H; Ochi, M; Sakai, H; Takeuchi, Y | 1 |
2 other study(ies) available for tyrosine and Action Myoclonus-Renal Failure Syndrome
| Article | Year |
|---|---|
Linkage analysis and exome sequencing identify a novel mutation in KCTD7 in patients with progressive myoclonus epilepsy with ataxia.
Topics: Adolescent; Ataxia; Child, Preschool; Chromosome Mapping; Chromosomes, Human, Pair 7; Cysteine; Electroencephalography; Exome; Female; Genetic Linkage; Humans; Infant; Male; Mutation; Myoclonic Epilepsies, Progressive; Potassium Channels; Tyrosine | 2014 |
Developmental changes in cerebrospinal fluid concentrations of monoamine-related substances in patients with dentatorubral-pallidoluysian atrophy.
Topics: Adolescent; Age Factors; Aging; Biogenic Monoamines; Case-Control Studies; Child; Child, Preschool; Chromatography, High Pressure Liquid; Female; Homovanillic Acid; Humans; Hydroxyindoleacetic Acid; Male; Methoxyhydroxyphenylglycol; Myoclonic Epilepsies, Progressive; Tryptophan; Tyrosine | 2001 |