Page last updated: 2024-10-19

inositol and Central Nervous System Demyelinating Diseases, Hereditary

inositol has been researched along with Central Nervous System Demyelinating Diseases, Hereditary in 1 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.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Tonduti, D1
Vanderver, A1
Berardinelli, A1
Schmidt, JL1
Collins, CD1
Novara, F1
Genni, AD1
Mita, A1
Triulzi, F1
Brunstrom-Hernandez, JE1
Zuffardi, O1
Balottin, U1
Orcesi, S1

Other Studies

1 other study available for inositol and Central Nervous System Demyelinating Diseases, Hereditary

ArticleYear
MCT8 deficiency: extrapyramidal symptoms and delayed myelination as prominent features.
    Journal of child neurology, 2013, Volume: 28, Issue:6

    Topics: Aspartic Acid; Basal Ganglia Diseases; Brain; Child, Preschool; Choline; Chromosomes, Human, X; Codo

2013