alanine has been researched along with Chorea Disorders in 4 studies
Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (25.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (75.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| COWIE, V | 1 |
| SEAKINS, JW | 1 |
| Chen, DH | 1 |
| Matsushita, M | 1 |
| Rainier, S | 1 |
| Meaney, B | 1 |
| Tisch, L | 1 |
| Feleke, A | 1 |
| Wolff, J | 1 |
| Lipe, H | 1 |
| Fink, J | 1 |
| Bird, TD | 1 |
| Raskind, WH | 1 |
| Stefanova, E | 1 |
| Djarmati, A | 1 |
| Momcilović, D | 1 |
| Dragasević, N | 1 |
| Svetel, M | 1 |
| Klein, C | 1 |
| Kostić, VS | 1 |
| Wiltshire, EJ | 1 |
| Poplawski, NK | 1 |
| Harbord, MG | 1 |
| Harrison, RJ | 1 |
| Fletcher, JM | 1 |
4 other studies available for alanine and Chorea Disorders
| Article | Year |
|---|---|
Urinary alanine excretor in a Huntington's chorea family.
Topics: Alanine; Body Fluids; Chorea; Humans; Huntington Disease | 1962 |
Presence of alanine-to-valine substitutions in myofibrillogenesis regulator 1 in paroxysmal nonkinesigenic dyskinesia: confirmation in 2 kindreds.
Topics: Alanine; Amino Acid Substitution; Chorea; Chromosome Mapping; Chromosomes, Human, Pair 2; DNA Mutati | 2005 |
Clinical characteristics of paroxysmal nonkinesigenic dyskinesia in Serbian family with Myofibrillogenesis regulator 1 gene mutation.
Topics: Adolescent; Adult; Alanine; Chorea; DNA Mutational Analysis; Family Health; Female; Humans; Male; Mi | 2006 |
Ornithine carbamoyltransferase deficiency presenting with chorea in a female.
Topics: Alanine; Chorea; Female; Glutamine; Humans; Infant; Ornithine Carbamoyltransferase Deficiency Diseas | 2000 |