inositol has been researched along with Ornithine Carbamoyltransferase Deficiency Disease 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.
Ornithine Carbamoyltransferase Deficiency Disease: An inherited urea cycle disorder associated with deficiency of the enzyme ORNITHINE CARBAMOYLTRANSFERASE, transmitted as an X-linked trait and featuring elevations of amino acids and ammonia in the serum. Clinical features, which are more prominent in males, include seizures, behavioral alterations, episodic vomiting, lethargy, and coma. (Menkes, Textbook of Child Neurology, 5th ed, pp49-50)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Takanashi, J | 1 |
| Kurihara, A | 1 |
| Tomita, M | 1 |
| Kanazawa, M | 1 |
| Yamamoto, S | 1 |
| Morita, F | 1 |
| Ikehira, H | 1 |
| Tanada, S | 1 |
| Kohno, Y | 1 |
| Gropman, AL | 1 |
| Seltzer, RR | 1 |
| Yudkoff, M | 1 |
| Sawyer, A | 1 |
| VanMeter, J | 1 |
| Fricke, ST | 1 |
2 other studies available for inositol and Ornithine Carbamoyltransferase Deficiency Disease
| Article | Year |
|---|---|
Distinctly abnormal brain metabolism in late-onset ornithine transcarbamylase deficiency.
Topics: Adolescent; Adult; Age of Onset; Brain; Case-Control Studies; Child; Child, Preschool; Choline; Fema | 2002 |
1H MRS allows brain phenotype differentiation in sisters with late onset ornithine transcarbamylase deficiency (OTCD) and discordant clinical presentations.
Topics: Adult; Age of Onset; Brain; Brain Chemistry; Cell Differentiation; Cognition Disorders; Female; Huma | 2008 |