trimethylamine has been researched along with Muscular Atrophy, Spinal in 1 studies
Muscular Atrophy, Spinal: A group of disorders marked by progressive degeneration of motor neurons in the spinal cord resulting in weakness and muscular atrophy, usually without evidence of injury to the corticospinal tracts. Diseases in this category include Werdnig-Hoffmann disease and later onset SPINAL MUSCULAR ATROPHIES OF CHILDHOOD, most of which are hereditary. (Adams et al., Principles of Neurology, 6th ed, p1089)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hsieh, TJ | 1 |
| Wang, CK | 1 |
| Chuang, HY | 1 |
| Jong, YJ | 1 |
| Li, CW | 1 |
| Liu, GC | 1 |
1 other study available for trimethylamine and Muscular Atrophy, Spinal
| Article | Year |
|---|---|
In vivo proton magnetic resonance spectroscopy assessment for muscle metabolism in neuromuscular diseases.
Topics: Adipose Tissue; Adolescent; Child; Child, Preschool; Creatine; Female; Humans; Magnetic Resonance Sp | 2007 |