2,4-diaminobutyric acid has been researched along with Amyotrophic Lateral Sclerosis in 2 studies
2,4-diaminobutyric acid: RN given refers to parent cpd without isomeric designation
2,4-diaminobutyric acid : A diamino acid that is butyric acid in which a hydrogen at position 2 and a hydrogen at position 4 are replaced by amino groups.
Amyotrophic Lateral Sclerosis: A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94)
| 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 |
|---|---|
| Combes, A | 1 |
| El Abdellaoui, S | 1 |
| Vial, J | 1 |
| Lagrange, E | 1 |
| Pichon, V | 1 |
| Cox, PA | 1 |
| Richer, R | 1 |
| Metcalf, JS | 1 |
| Banack, SA | 1 |
| Codd, GA | 1 |
| Bradley, WG | 1 |
2 other studies available for 2,4-diaminobutyric acid and Amyotrophic Lateral Sclerosis
| Article | Year |
|---|---|
Development of an analytical procedure for quantifying the underivatized neurotoxin β-N-methylamino-L-alanine in brain tissues.
Topics: Amino Acids, Diamino; Aminobutyrates; Amyotrophic Lateral Sclerosis; Animals; Cattle; Chromatography | 2014 |
Cyanobacteria and BMAA exposure from desert dust: a possible link to sporadic ALS among Gulf War veterans.
Topics: Amino Acids, Diamino; Amino Acids, Dicarboxylic; Aminobutyrates; Amyotrophic Lateral Sclerosis; Chro | 2009 |