allantoin has been researched along with Hepatolenticular Degeneration in 3 studies
Hepatolenticular Degeneration: A rare autosomal recessive disease characterized by the deposition of copper in the BRAIN; LIVER; CORNEA; and other organs. It is caused by defects in the ATP7B gene encoding copper-transporting ATPase 2 (EC 3.6.3.4), also known as the Wilson disease protein. The overload of copper inevitably leads to progressive liver and neurological dysfunction such as LIVER CIRRHOSIS; TREMOR; ATAXIA and intellectual deterioration. Hepatic dysfunction may precede neurologic dysfunction by several years.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ogihara, T | 2 |
| Tamai, H | 1 |
| Ogihara, H | 1 |
| Miki, M | 1 |
| Yasuda, H | 1 |
| Mino, M | 1 |
| Sorensen, LB | 1 |
1 review available for allantoin and Hepatolenticular Degeneration
| Article | Year |
|---|---|
[Allantoin].
Topics: Allantoin; Arthritis, Rheumatoid; Biomarkers; Chromatography, High Pressure Liquid; Chromatography, | 2005 |
2 other studies available for allantoin and Hepatolenticular Degeneration
| Article | Year |
|---|---|
Plasma copper and antioxidant status in Wilson's disease.
Topics: Allantoin; Antioxidants; Ascorbic Acid; Biomarkers; Ceruloplasmin; Child; Copper; Female; Free Radic | 1995 |
Role of the intestinal tract in the elimination of uric acid.
Topics: Allantoin; Ammonia; Carbon Dioxide; Carbon Isotopes; Digestive System Physiological Phenomena; Feces | 1965 |