alanine has been researched along with Frontotemporal Lobar Degeneration 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.
Frontotemporal Lobar Degeneration: Heterogeneous group of neurodegenerative disorders characterized by frontal and temporal lobe atrophy associated with neuronal loss, gliosis, and dementia. Patients exhibit progressive changes in social, behavioral, and/or language function. Multiple subtypes or forms are recognized based on presence or absence of TAU PROTEIN inclusions. FTLD includes three clinical syndromes: FRONTOTEMPORAL DEMENTIA, semantic dementia, and PRIMARY PROGRESSIVE NONFLUENT APHASIA.
| Excerpt | Relevance | Reference |
|---|---|---|
| "In these families, FTLD cosegregates with ALS." | 1.36 | Amyotrophic lateral sclerosis-frontotemporal lobar dementia in 3 families with p.Ala382Thr TARDBP mutations. ( Borghero, G; Brunetti, M; Calvo, A; Chiò, A; Cistaro, A; Marrosu, MG; Moglia, C; Montuschi, A; Murru, MR; Mutani, R; Ossola, I; Restagno, G; Schymick, JC; Ticca, A; Traynor, BJ, 2010) |
| 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 |
|---|---|
| Chiò, A | 1 |
| Calvo, A | 1 |
| Moglia, C | 1 |
| Restagno, G | 1 |
| Ossola, I | 1 |
| Brunetti, M | 1 |
| Montuschi, A | 1 |
| Cistaro, A | 1 |
| Ticca, A | 1 |
| Traynor, BJ | 1 |
| Schymick, JC | 1 |
| Mutani, R | 1 |
| Marrosu, MG | 1 |
| Murru, MR | 1 |
| Borghero, G | 1 |
1 other study available for alanine and Frontotemporal Lobar Degeneration
| Article | Year |
|---|---|
Amyotrophic lateral sclerosis-frontotemporal lobar dementia in 3 families with p.Ala382Thr TARDBP mutations.
Topics: Adult; Aged; Alanine; Amyotrophic Lateral Sclerosis; Brain; Cognition Disorders; DNA-Binding Protein | 2010 |