inositol has been researched along with Gelineau Syndrome in 3 studies
Inositol: An isomer of glucose that has traditionally been considered to be a B vitamin although it has an uncertain status as a vitamin and a deficiency syndrome has not been identified in man. (From Martindale, The Extra Pharmacopoeia, 30th ed, p1379) Inositol phospholipids are important in signal transduction.
inositol : Any cyclohexane-1,2,3,4,5,6-hexol.
1D-chiro-inositol : Belonging to the inositol family of compounds, D-chiro-inositol (DCI) is an isomer of glucose. It is an important secondary messenger in insulin signal transduction.
muco-inositol : An inositol that is cyclohexane-1,2,3,4,5,6-hexol having a (1R,2R,3r,4R,5S,6r)-configuration.
| Excerpt | Relevance | Reference |
|---|---|---|
| " As neuronal loss and gliosis have been described in narcolepsy, metabolites of primary interest are N-acetylaspartate (NAA), a marker of neuronal integrity and myo-Inositol (ml), a glial marker and second messenger involved in the regulation of intracellular calcium." | 3.75 | Evidence for metabolic hypothalamo-amygdala dysfunction in narcolepsy. ( Bassetti, CL; Boesiger, P; Dydak, U; Khatami, R; Meier, D; Poryazova, R; Schnepf, B; Werth, E, 2009) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Moghadam, KK | 1 |
| Pizza, F | 1 |
| Tonon, C | 1 |
| Lodi, R | 1 |
| Carelli, V | 1 |
| Poli, F | 1 |
| Franceschini, C | 1 |
| Barboni, P | 1 |
| Seri, M | 1 |
| Ferrari, S | 1 |
| La Morgia, C | 1 |
| Testa, C | 1 |
| Cornelio, F | 1 |
| Liguori, R | 1 |
| Winkelmann, J | 1 |
| Lin, L | 1 |
| Mignot, E | 1 |
| Plazzi, G | 1 |
| Picchioni, D | 1 |
| Poryazova, R | 1 |
| Schnepf, B | 1 |
| Werth, E | 1 |
| Khatami, R | 1 |
| Dydak, U | 1 |
| Meier, D | 1 |
| Boesiger, P | 1 |
| Bassetti, CL | 1 |
3 other studies available for inositol and Gelineau Syndrome
| Article | Year |
|---|---|
Polysomnographic and neurometabolic features may mark preclinical autosomal dominant cerebellar ataxia, deafness, and narcolepsy due to a mutation in the DNA (cytosine-5-)-methyltransferase gene, DNMT1.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Asymptomatic Diseases; Brain; Cerebellar Ataxia; Cerebel | 2014 |
Using magnetic resonance spectroscopy in narcolepsy to study the limbic mechanisms of cataplexy.
Topics: Amygdala; Aspartic Acid; Cataplexy; Energy Metabolism; Humans; Hypothalamus; Inositol; Magnetic Reso | 2009 |
Evidence for metabolic hypothalamo-amygdala dysfunction in narcolepsy.
Topics: Adult; Amygdala; Aspartic Acid; Cataplexy; Creatine; Dominance, Cerebral; Energy Metabolism; Female; | 2009 |