alanine has been researched along with Spastic Paraplegia, Hereditary in 1 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.
Spastic Paraplegia, Hereditary: A group of inherited diseases that share similar phenotypes but are genetically diverse. Different genetic loci for autosomal recessive, autosomal dominant, and x-linked forms of hereditary spastic paraplegia have been identified. Clinically, patients present with slowly progressive distal limb weakness and lower extremity spasticity. Peripheral sensory neurons may be affected in the later stages of the disease. (J Neurol Neurosurg Psychiatry 1998 Jan;64(1):61-6; Curr Opin Neurol 1997 Aug;10(4):313-8)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Roxburgh, RH | 1 |
| Marquis-Nicholson, R | 1 |
| Ashton, F | 1 |
| George, AM | 1 |
| Lea, RA | 1 |
| Eccles, D | 1 |
| Mossman, S | 1 |
| Bird, T | 1 |
| van Gassen, KL | 1 |
| Kamsteeg, EJ | 1 |
| Love, DR | 1 |
1 other study available for alanine and Spastic Paraplegia, Hereditary
| Article | Year |
|---|---|
The p.Ala510Val mutation in the SPG7 (paraplegin) gene is the most common mutation causing adult onset neurogenetic disease in patients of British ancestry.
Topics: Adult; Age of Onset; Alanine; ATPases Associated with Diverse Cellular Activities; Female; Genetic P | 2013 |