Page last updated: 2024-10-20

thiamine and Motor Neuron Disease

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)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (50.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's1 (50.00)2.80

Authors

AuthorsStudies
Zambon, AA1
Ghezzi, D1
Baldoli, C1
Cutillo, G1
Fontana, K1
Sofia, V1
Patricelli, MG1
Nasca, A1
Vinci, S1
Spiga, I1
Lamantea, E1
Fanelli, GF1
Sora, MGN1
Rovelli, R1
Poloniato, A1
Carrera, P1
Filippi, M1
Barera, G1
Bonne, G1
Benelli, C1
De Meirleir, L1
Lissens, W1
Chaussain, M1
Diry, M1
Clot, JP1
Ponsot, G1
Geoffroy, V1
Leroux, JP1

Other Studies

2 other studies available for thiamine and Motor Neuron Disease

ArticleYear
Expanding the spectrum of neonatal-onset AIFM1-associated disorders.
    Annals of clinical and translational neurology, 2023, Volume: 10, Issue:10

    Topics: Apoptosis Inducing Factor; Humans; Infant, Newborn; Male; Mitochondria; Mitochondrial Encephalomyopa

2023
E1 pyruvate dehydrogenase deficiency in a child with motor neuropathy.
    Pediatric research, 1993, Volume: 33, Issue:3

    Topics: Base Sequence; Carnitine; Child; DNA; DNA Mutational Analysis; Drug Therapy, Combination; Humans; Ly

1993