hydroxyproline has been researched along with Gaucher Disease in 1 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.
Gaucher Disease: An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ciana, G | 1 |
| Martini, C | 1 |
| Leopaldi, A | 1 |
| Tamaro, G | 1 |
| Katouzian, F | 1 |
| Ronfani, L | 1 |
| Bembi, B | 1 |
1 other study available for hydroxyproline and Gaucher Disease
| Article | Year |
|---|---|
Bone marker alterations in patients with type 1 Gaucher disease.
Topics: Absorptiometry, Photon; Adult; Alkaline Phosphatase; Amino Acids; Biomarkers; Bone Density; Bone Rem | 2003 |