hydroxyproline has been researched along with Hepatolenticular Degeneration in 2 studies
Hydroxyproline: A hydroxylated form of the imino acid proline. A deficiency in ASCORBIC ACID can result in impaired hydroxyproline formation.
hydroxyproline : A proline derivative that is proline substituted by at least one hydroxy group.
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 | 2 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Asatoor, AM | 2 |
| Milne, MD | 1 |
| Walshe, JM | 2 |
| Miline, MD | 1 |
2 other studies available for hydroxyproline and Hepatolenticular Degeneration
| Article | Year |
|---|---|
Peptiduria in the Fanconi syndrome.
Topics: Animals; Fanconi Syndrome; Hepatolenticular Degeneration; Humans; Hydroxyproline; Maleates; Peptides | 1977 |
Urinary excretion of peptides and of hydroxyproline in Wilson's disease.
Topics: Adolescent; Adult; Amino Acids; Child; Collagen; Copper; Female; Hepatolenticular Degeneration; Huma | 1976 |