inositol has been researched along with Muscular Dystrophy, Duchenne in 2 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.
Muscular Dystrophy, Duchenne: An X-linked recessive muscle disease caused by an inability to synthesize DYSTROPHIN, which is involved with maintaining the integrity of the sarcolemma. Muscle fibers undergo a process that features degeneration and regeneration. Clinical manifestations include proximal weakness in the first few years of life, pseudohypertrophy, cardiomyopathy (see MYOCARDIAL DISEASES), and an increased incidence of impaired mentation. Becker muscular dystrophy is a closely related condition featuring a later onset of disease (usually adolescence) and a slowly progressive course. (Adams et al., Principles of Neurology, 6th ed, p1415)
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (50.00) | 24.3611 |
2020's | 1 (50.00) | 2.80 |
Authors | Studies |
---|---|
Merckx, C | 1 |
Cosemans, G | 1 |
Zschüntzsch, J | 1 |
Raedt, R | 1 |
Schmidt, J | 1 |
De Paepe, B | 1 |
De Bleecker, JL | 1 |
Doorenweerd, N | 1 |
Hooijmans, M | 1 |
Schubert, SA | 1 |
Webb, AG | 1 |
Straathof, CS | 1 |
van Zwet, EW | 1 |
van Buchem, MA | 1 |
Verschuuren, JJ | 1 |
Hendriksen, JG | 1 |
Niks, EH | 1 |
Kan, HE | 1 |
2 other studies available for inositol and Muscular Dystrophy, Duchenne
Article | Year |
---|---|
Description of Osmolyte Pathways in Maturing
Topics: Animals; Inositol; Mice; Mice, Inbred C57BL; Mice, Inbred mdx; Muscle, Skeletal; Muscular Dystrophy, | 2022 |
Proton Magnetic Resonance Spectroscopy Indicates Preserved Cerebral Biochemical Composition in Duchenne Muscular Dystrophy Patients.
Topics: Adolescent; Aquaporin 4; Aspartic Acid; Brain; Case-Control Studies; Cerebellum; Child; Choline; Cre | 2017 |