taurine has been researched along with Gaucher Disease in 1 studies
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.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Gaucher disease is caused by an autosomal-recessive deficiency of glucocerebrosidase." | 5.31 | Decrease of plasma taurine in Gaucher disease and its sustained correction during enzyme replacement therapy. ( Häussinger, D; Mönnighoff, I; vom Dahl, S, 2000) |
| "Gaucher disease is caused by an autosomal-recessive deficiency of glucocerebrosidase." | 1.31 | Decrease of plasma taurine in Gaucher disease and its sustained correction during enzyme replacement therapy. ( Häussinger, D; Mönnighoff, I; vom Dahl, S, 2000) |
| 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 |
|---|---|
| vom Dahl, S | 1 |
| Mönnighoff, I | 1 |
| Häussinger, D | 1 |
1 other study available for taurine and Gaucher Disease
| Article | Year |
|---|---|
Decrease of plasma taurine in Gaucher disease and its sustained correction during enzyme replacement therapy.
Topics: Adult; Gaucher Disease; Glucosylceramidase; Humans; Middle Aged; Taurine | 2000 |