thiamine has been researched along with Motor Neuron Disease in 2 studies
thiamine(1+) : A primary alcohol that is 1,3-thiazol-3-ium substituted by (4-amino-2-methylpyrimidin-5-yl)methyl, methyl and 2-hydroxyethyl groups at positions 3, 4 and 5, respectively.
Motor Neuron Disease: Diseases characterized by a selective degeneration of the motor neurons of the spinal cord, brainstem, or motor cortex. Clinical subtypes are distinguished by the major site of degeneration. In AMYOTROPHIC LATERAL SCLEROSIS there is involvement of upper, lower, and brainstem motor neurons. In progressive muscular atrophy and related syndromes (see MUSCULAR ATROPHY, SPINAL) the motor neurons in the spinal cord are primarily affected. With progressive bulbar palsy (BULBAR PALSY, PROGRESSIVE), the initial degeneration occurs in the brainstem. In primary lateral sclerosis, the cortical neurons are affected in isolation. (Adams et al., Principles of Neurology, 6th ed, p1089)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Zambon, AA | 1 |
| Ghezzi, D | 1 |
| Baldoli, C | 1 |
| Cutillo, G | 1 |
| Fontana, K | 1 |
| Sofia, V | 1 |
| Patricelli, MG | 1 |
| Nasca, A | 1 |
| Vinci, S | 1 |
| Spiga, I | 1 |
| Lamantea, E | 1 |
| Fanelli, GF | 1 |
| Sora, MGN | 1 |
| Rovelli, R | 1 |
| Poloniato, A | 1 |
| Carrera, P | 1 |
| Filippi, M | 1 |
| Barera, G | 1 |
| Bonne, G | 1 |
| Benelli, C | 1 |
| De Meirleir, L | 1 |
| Lissens, W | 1 |
| Chaussain, M | 1 |
| Diry, M | 1 |
| Clot, JP | 1 |
| Ponsot, G | 1 |
| Geoffroy, V | 1 |
| Leroux, JP | 1 |
2 other studies available for thiamine and Motor Neuron Disease
| Article | Year |
|---|---|
Expanding the spectrum of neonatal-onset AIFM1-associated disorders.
Topics: Apoptosis Inducing Factor; Humans; Infant, Newborn; Male; Mitochondria; Mitochondrial Encephalomyopa | 2023 |
E1 pyruvate dehydrogenase deficiency in a child with motor neuropathy.
Topics: Base Sequence; Carnitine; Child; DNA; DNA Mutational Analysis; Drug Therapy, Combination; Humans; Ly | 1993 |